1 00:00:00,070 --> 00:00:01,780 The following content is provided 2 00:00:01,780 --> 00:00:04,030 under a Creative Commons license. 3 00:00:04,030 --> 00:00:06,880 Your support will help MIT OpenCourseWare continue 4 00:00:06,880 --> 00:00:10,740 to offer high quality educational resources for free. 5 00:00:10,740 --> 00:00:13,350 To make a donation or view additional materials 6 00:00:13,350 --> 00:00:17,237 from hundreds of MIT courses, visit MIT OpenCourseWare 7 00:00:17,237 --> 00:00:17,862 at ocw.mit.edu. 8 00:00:24,840 --> 00:00:25,960 PROFESSOR: Good afternoon. 9 00:00:30,170 --> 00:00:34,190 The title here is the topic for our class today. 10 00:00:34,190 --> 00:00:38,720 We want to discuss formally the derivation Optical Bloch 11 00:00:38,720 --> 00:00:43,290 Equations, but usually when I teach you something, 12 00:00:43,290 --> 00:00:46,240 I have a general concept in mind and the concept right now here 13 00:00:46,240 --> 00:00:52,080 is, how can we get from unitary time evolution of a quantum 14 00:00:52,080 --> 00:00:55,740 system to rate equations anticipation. 15 00:00:55,740 --> 00:00:59,250 And this is sort of the subject of master equation 16 00:00:59,250 --> 00:01:03,460 open system dynamics, and this cartoon sort of tells you 17 00:01:03,460 --> 00:01:05,489 what you want to do. 18 00:01:05,489 --> 00:01:10,990 We have a total system, which is one part we are interested in, 19 00:01:10,990 --> 00:01:14,163 and the other one, often it has many, many degrees of freedom, 20 00:01:14,163 --> 00:01:16,140 and we don't want to keep track of them. 21 00:01:16,140 --> 00:01:18,380 But they have one Hamiltonian. 22 00:01:18,380 --> 00:01:22,330 But we are only interested in how our atomic system evolves, 23 00:01:22,330 --> 00:01:24,550 and we want to find an equation, which 24 00:01:24,550 --> 00:01:26,680 is no longer a Schrodinger equation. 25 00:01:26,680 --> 00:01:30,950 How does an initial density matrix describing our system 26 00:01:30,950 --> 00:01:32,780 develop with time? 27 00:01:32,780 --> 00:01:37,050 And as we will see, in general, it follows a master equation, 28 00:01:37,050 --> 00:01:39,710 and we want to discuss what are general principles 29 00:01:39,710 --> 00:01:41,560 of such equations. 30 00:01:41,560 --> 00:01:45,080 But it's very important here is that we are not 31 00:01:45,080 --> 00:01:47,770 keeping track of what happens in the environment, 32 00:01:47,770 --> 00:01:51,140 and that's associated here with a little bucket or trash can. 33 00:01:51,140 --> 00:01:54,350 Every result photons or such are measured, 34 00:01:54,350 --> 00:01:59,040 the environment is constantly projected on a measurement 35 00:01:59,040 --> 00:02:03,200 basis, and therefore, re-introduce probabilistic 36 00:02:03,200 --> 00:02:07,970 element into the part we don't observe mainly 37 00:02:07,970 --> 00:02:12,470 the part which characterizes the atoms. 38 00:02:12,470 --> 00:02:19,690 So for that we need the formalism of density matrix, 39 00:02:19,690 --> 00:02:26,065 and that's where we want to start. 40 00:02:29,850 --> 00:02:34,540 At the end of last lecture, I reminded you 41 00:02:34,540 --> 00:02:36,880 that the density matrix can always 42 00:02:36,880 --> 00:02:39,700 be written as an ensemble where you 43 00:02:39,700 --> 00:02:42,520 say you have a certain probability for certain rate 44 00:02:42,520 --> 00:02:45,160 function. 45 00:02:45,160 --> 00:02:48,660 This is always possible, but it is not unique. 46 00:02:48,660 --> 00:02:52,580 So each of you could actually create the same density matrix 47 00:02:52,580 --> 00:02:55,460 by preparing a number of quantum states 48 00:02:55,460 --> 00:02:57,420 with a certain probability and saying 49 00:02:57,420 --> 00:02:58,960 this is my density matrix. 50 00:02:58,960 --> 00:03:01,700 And also each of you has prepared different quantum 51 00:03:01,700 --> 00:03:02,630 states. 52 00:03:02,630 --> 00:03:04,640 If you sum them up in that same way, 53 00:03:04,640 --> 00:03:09,280 you get the same density matrix and therefore, all observables 54 00:03:09,280 --> 00:03:12,280 or measurements you will do on your ensemble in the future 55 00:03:12,280 --> 00:03:15,320 will be identical because the density matrix is 56 00:03:15,320 --> 00:03:17,890 a full description of the system. 57 00:03:17,890 --> 00:03:20,705 So at that level, it may look sort of very trivial 58 00:03:20,705 --> 00:03:23,000 that we have different unraveling. 59 00:03:23,000 --> 00:03:25,130 Unraveling means you look microscopically 60 00:03:25,130 --> 00:03:27,140 what is behind the density matrix, 61 00:03:27,140 --> 00:03:28,640 but in your homework assignment, you 62 00:03:28,640 --> 00:03:32,970 will all show that you can have a system which have very, very 63 00:03:32,970 --> 00:03:34,990 different dissipation mechanisms, 64 00:03:34,990 --> 00:03:37,290 but they're described by the same equation. 65 00:03:37,290 --> 00:03:41,490 So therefore, it's physically not possible 66 00:03:41,490 --> 00:03:45,280 to distinguish by just measuring the density matrix what 67 00:03:45,280 --> 00:03:46,810 causes a dissipation. 68 00:03:46,810 --> 00:03:49,400 Of course, if you know what causes a dissipation, 69 00:03:49,400 --> 00:03:50,990 fluctuating fields or collisions, 70 00:03:50,990 --> 00:03:53,630 you know more than the density matrix knows. 71 00:03:57,220 --> 00:04:01,900 Any questions about density matrix or the agenda 72 00:04:01,900 --> 00:04:03,240 we want to go through today? 73 00:04:07,360 --> 00:04:12,160 Just a quick reminder and since this was covered in 8421, 74 00:04:12,160 --> 00:04:18,410 and most of you know about it, I pre-wrote the slides. 75 00:04:18,410 --> 00:04:20,800 The density matrix is a time evolution. 76 00:04:20,800 --> 00:04:25,160 There is one which is sort trivial and covered in more 77 00:04:25,160 --> 00:04:29,450 elementary takes, and this is the Hamiltonian evolution, 78 00:04:29,450 --> 00:04:30,890 and I'm sure you've seen it. 79 00:04:30,890 --> 00:04:33,250 The time evolution, the unitary time evolution 80 00:04:33,250 --> 00:04:35,190 involves the commutative of the Hamiltonian 81 00:04:35,190 --> 00:04:40,600 with a density matrix, and later on, we 82 00:04:40,600 --> 00:04:43,900 want to specialize including dissipation, including 83 00:04:43,900 --> 00:04:48,170 the environment to the evolution of a tool evolutionary system 84 00:04:48,170 --> 00:04:51,120 driven by a monochromatic field 85 00:04:51,120 --> 00:05:01,680 And this the famous Jaynes-Cummings Hamiltonian, 86 00:05:01,680 --> 00:05:05,920 and we can characterize this system by a density matrix, 87 00:05:05,920 --> 00:05:08,670 but will be very important is that we distinguish 88 00:05:08,670 --> 00:05:11,240 between populations, the diagonal parts, 89 00:05:11,240 --> 00:05:13,350 and the coherences. 90 00:05:13,350 --> 00:05:17,080 And if you simply put this density matrix 91 00:05:17,080 --> 00:05:32,980 into this equation, you find the time evolution of the system, 92 00:05:32,980 --> 00:05:36,630 and we will refer to that result later on. 93 00:05:36,630 --> 00:05:39,470 Many of you have seen it in 8421. 94 00:05:39,470 --> 00:05:42,470 we can parametrize the density matrix 95 00:05:42,470 --> 00:05:44,160 for the two-level system. 96 00:05:44,160 --> 00:05:46,015 So we can parametrize the densities 97 00:05:46,015 --> 00:05:49,080 of the two-level system by a local vector, 98 00:05:49,080 --> 00:05:52,520 r, which is defined by this equation. 99 00:05:52,520 --> 00:05:56,550 And then the equation of motion is simply 100 00:05:56,550 --> 00:06:00,730 the rotation of a Bloch vector on the Bloch sphere, 101 00:06:00,730 --> 00:06:04,770 and it has a rotational axis, which 102 00:06:04,770 --> 00:06:08,360 is given by-- the undriven system 103 00:06:08,360 --> 00:06:10,270 rotates around the z-axis. 104 00:06:10,270 --> 00:06:12,040 This is just e to the i omega naught 105 00:06:12,040 --> 00:06:15,280 t, the normal evolution of the free system. 106 00:06:15,280 --> 00:06:19,440 But if you divide it with a monochromatic field 107 00:06:19,440 --> 00:06:23,060 rotation over the x-axis and the x-axis, of course, 108 00:06:23,060 --> 00:06:25,545 can take your two-level system, and flip it from the ground 109 00:06:25,545 --> 00:06:26,970 to the excited state. 110 00:06:26,970 --> 00:06:30,770 So it's just a reminder of the simple unitary time evolution, 111 00:06:30,770 --> 00:06:33,360 but now we want to add dissipation on top of it. 112 00:06:36,300 --> 00:06:52,240 And what I've decided that before I discuss 113 00:06:52,240 --> 00:06:55,500 with you Optical Bloch Equation and master equation in general, 114 00:06:55,500 --> 00:06:58,840 I want to give you a very simple model. 115 00:06:58,840 --> 00:07:01,570 I really like simple models which 116 00:07:01,570 --> 00:07:05,080 capture the essence of what you are going to discuss. 117 00:07:05,080 --> 00:07:12,750 So what I want to use is I want to use a beam splitter 118 00:07:12,750 --> 00:07:28,520 model I formulated for photons, but it would also immediately 119 00:07:28,520 --> 00:07:30,830 apply to atoms. 120 00:07:30,830 --> 00:07:33,210 And this model, what I like about it, 121 00:07:33,210 --> 00:07:35,910 it has all the ingredients of integration of the master 122 00:07:35,910 --> 00:07:38,990 equation we'll do later on without the kind 123 00:07:38,990 --> 00:07:42,640 of many indices and summations and integration, 124 00:07:42,640 --> 00:07:46,370 but it captures every single bit of what is important. 125 00:07:46,370 --> 00:07:50,640 And I usually like to present exactly solvable, simple models 126 00:07:50,640 --> 00:07:52,780 where you get it, and then I can go a little bit 127 00:07:52,780 --> 00:07:54,300 faster for the general derivation 128 00:07:54,300 --> 00:07:58,097 because you know exactly what the more complicated equations, 129 00:07:58,097 --> 00:07:58,930 what they are doing. 130 00:08:02,360 --> 00:08:09,160 So in other words, what I want to derive for you is 131 00:08:09,160 --> 00:08:11,175 we want to have the following situation. 132 00:08:11,175 --> 00:08:14,260 We have a beam splitter, and we know everything 133 00:08:14,260 --> 00:08:16,590 about beam splitters because we talked about them 134 00:08:16,590 --> 00:08:18,860 in the first part of the course, and we 135 00:08:18,860 --> 00:08:22,680 have a wave function, which is the input, 136 00:08:22,680 --> 00:08:25,390 and this is a photon. 137 00:08:25,390 --> 00:08:29,260 And we want to understand after the beam splitter, 138 00:08:29,260 --> 00:08:31,820 how has the system evolved. 139 00:08:31,820 --> 00:08:34,870 In general, it will be a density matrix, 140 00:08:34,870 --> 00:08:36,464 and what you want to find out is, 141 00:08:36,464 --> 00:08:39,200 what is the equation for the density matrix. 142 00:08:39,200 --> 00:08:42,400 Maybe this density matrix goes through the next beam splitter 143 00:08:42,400 --> 00:08:44,510 and then we want to know what comes out of it. 144 00:08:44,510 --> 00:08:47,950 And all we have to apply is the formalism 145 00:08:47,950 --> 00:08:52,680 we developed for the beam splitter earlier in the course. 146 00:08:52,680 --> 00:08:55,750 Of course, the beam splitter is not as harmless 147 00:08:55,750 --> 00:08:56,970 as it looks like. 148 00:08:56,970 --> 00:09:03,710 There is another part and another part one here 149 00:09:03,710 --> 00:09:07,530 brings in the environment, and for the environment, 150 00:09:07,530 --> 00:09:09,300 we will use the vacuum. 151 00:09:09,300 --> 00:09:11,260 That's the simplest environment. 152 00:09:11,260 --> 00:09:12,810 It's actually important environment 153 00:09:12,810 --> 00:09:16,090 because it is the environment we will use all the time when 154 00:09:16,090 --> 00:09:17,970 we discuss spontaneous emission. 155 00:09:17,970 --> 00:09:21,330 We send photons into the nirvana, into the vacuum 156 00:09:21,330 --> 00:09:24,220 and they disappear, and this is our modified. 157 00:09:24,220 --> 00:09:27,400 But the other one which is often not so explicit. 158 00:09:27,400 --> 00:09:29,860 If you send your photons away, you're 159 00:09:29,860 --> 00:09:31,800 not keeping track of what happens, 160 00:09:31,800 --> 00:09:34,510 but you could as well perform a measurement, 161 00:09:34,510 --> 00:09:36,360 and this is what we put in here. 162 00:09:36,360 --> 00:09:42,630 We say those photons hit a bucket or detector 163 00:09:42,630 --> 00:09:44,300 and measure them, we observe them. 164 00:09:44,300 --> 00:09:46,140 There's nothing else we do with them, 165 00:09:46,140 --> 00:09:49,040 so we can as well measure them, and this being immediately 166 00:09:49,040 --> 00:09:53,281 lead to the equation for the density matrix. 167 00:09:53,281 --> 00:09:54,780 So this is what you want to discuss, 168 00:09:54,780 --> 00:09:56,980 and it will have all the ingredients later 169 00:09:56,980 --> 00:09:59,390 on in a mathematically simple form 170 00:09:59,390 --> 00:10:02,270 for the derivation of master equation. 171 00:10:02,270 --> 00:10:09,170 So let's consider a similar photon for that. 172 00:10:12,580 --> 00:10:16,630 So the wave function, this is superposition 173 00:10:16,630 --> 00:10:20,950 of no photon and 1 photon, and the coefficients 174 00:10:20,950 --> 00:10:23,930 are alpha and beta. 175 00:10:23,930 --> 00:10:28,630 And just for simplifying notation, 176 00:10:28,630 --> 00:10:31,820 I pick alpha and beta to be real. 177 00:10:31,820 --> 00:10:44,640 So what do we expect to happen at the beam splitter? 178 00:10:44,640 --> 00:10:48,175 Well, there's a probability that the photon gets reflected. 179 00:10:54,100 --> 00:10:58,760 Probability to reflect the photon 180 00:10:58,760 --> 00:11:00,500 and therefore to observe the photon. 181 00:11:06,470 --> 00:11:10,940 This probability is, of course, beta square-- the probability 182 00:11:10,940 --> 00:11:15,280 that we have a photon to begin with-- and then the beam 183 00:11:15,280 --> 00:11:18,560 splitter, remember we categorized the beam 184 00:11:18,560 --> 00:11:21,280 splitter with angle sine theta cosine theta. 185 00:11:21,280 --> 00:11:23,720 Sine theta was the reflection amplitude, 186 00:11:23,720 --> 00:11:26,470 cosine theta, the transmission amplitude. 187 00:11:26,470 --> 00:11:30,940 So this probability, which I call P1 188 00:11:30,940 --> 00:11:37,660 is the probability for reflection and for measurement. 189 00:11:37,660 --> 00:11:42,460 And now naively you would think what 190 00:11:42,460 --> 00:11:45,270 happens after the system has passed through the beam 191 00:11:45,270 --> 00:11:49,170 splitter, with a probability of P1, we've measured the photon. 192 00:11:49,170 --> 00:11:51,980 We know for sure there is no photon left. 193 00:11:51,980 --> 00:11:56,930 The system is in the vacuum state, 194 00:11:56,930 --> 00:11:59,980 but then you would say, well, maybe with probability 195 00:11:59,980 --> 00:12:05,030 1 minus P1, we have not measured anything. 196 00:12:05,030 --> 00:12:07,480 Nothing has happened to the wave function, 197 00:12:07,480 --> 00:12:09,760 and that means the wave function just continuous. 198 00:12:12,570 --> 00:12:17,750 Well as we will see, this is wrong. 199 00:12:17,750 --> 00:12:19,640 We are missing something. 200 00:12:19,640 --> 00:12:24,730 What we are actually missing is that if you measure nothing, 201 00:12:24,730 --> 00:12:26,460 the wave function is not sine. 202 00:12:26,460 --> 00:12:29,540 The possibility that we could have measured something, 203 00:12:29,540 --> 00:12:31,930 changes the wave function. 204 00:12:31,930 --> 00:12:36,260 I will comment on that in much more detail in a few lectures 205 00:12:36,260 --> 00:12:38,290 down the road when I derive for you 206 00:12:38,290 --> 00:12:40,040 quantum Monte Carlo wave function. 207 00:12:40,040 --> 00:12:42,450 I will have a wonderful discussions with you 208 00:12:42,450 --> 00:12:46,530 about how does non-observation change a wave function. 209 00:12:46,530 --> 00:12:49,190 So we will talk about the physics behind it 210 00:12:49,190 --> 00:12:50,580 in some more detail. 211 00:12:50,580 --> 00:12:54,150 Right now, I don't want to get into this discussion. 212 00:12:54,150 --> 00:12:56,850 I simply want to use our beam splitter equation, 213 00:12:56,850 --> 00:13:02,310 so we can just take the beam splitter equation and apply it. 214 00:13:02,310 --> 00:13:19,800 So our output state is obtained by taking 215 00:13:19,800 --> 00:13:23,510 the operator for our beam splitter, 216 00:13:23,510 --> 00:13:29,230 and maybe you remember that the propagation for beam splitter 217 00:13:29,230 --> 00:13:31,580 was discovered by an operator, which 218 00:13:31,580 --> 00:13:37,020 had a dagger b dagger a in the exponent. 219 00:13:37,020 --> 00:13:39,195 a and b are the two input nodes. 220 00:13:42,240 --> 00:13:46,540 And the angle of the beam splitter, 221 00:13:46,540 --> 00:13:49,700 which interpolates between 0% and 100% reflection 222 00:13:49,700 --> 00:13:52,180 transmission is theta. 223 00:13:52,180 --> 00:13:55,090 And we're now looking for the output 224 00:13:55,090 --> 00:13:58,010 state of the total system. 225 00:13:58,010 --> 00:14:00,190 We're not performing the measurement yet, 226 00:14:00,190 --> 00:14:08,330 and this is now acting on the total system, which 227 00:14:08,330 --> 00:14:11,110 is the cross product of our photon system, 228 00:14:11,110 --> 00:14:13,010 of our system of interest. 229 00:14:13,010 --> 00:14:15,940 And the other input, which we call 230 00:14:15,940 --> 00:14:19,430 the environment or the vacuum, is 0. 231 00:14:19,430 --> 00:14:25,096 Well, look a few weeks back, we have done that all. 232 00:14:25,096 --> 00:14:32,360 The output state is, well, there was a probability, alpha, 233 00:14:32,360 --> 00:14:38,410 that we had no photon in the state psi. 234 00:14:38,410 --> 00:14:40,340 And if we have no photon in the state psi 235 00:14:40,340 --> 00:14:43,500 and no photon in the vacuum, this is the state 0, 0. 236 00:14:46,770 --> 00:14:50,240 What I denote here with this second place 237 00:14:50,240 --> 00:14:51,120 is the environment. 238 00:14:53,750 --> 00:14:57,510 And now we have one photon. 239 00:14:57,510 --> 00:15:00,920 We have exactly one photon with the amplitude beta, 240 00:15:00,920 --> 00:15:06,810 and this photon is split with cosine theta transmitted 241 00:15:06,810 --> 00:15:10,850 and with phi theta reflected. 242 00:15:10,850 --> 00:15:15,350 If you transmit it, we have 1, 0. 243 00:15:15,350 --> 00:15:19,210 If we reflect it, we have 0, 1. 244 00:15:19,210 --> 00:15:23,399 And again, this is the environment, 245 00:15:23,399 --> 00:15:25,065 and here is a photon in the environment. 246 00:15:30,240 --> 00:15:33,330 So let me just be clear that this 247 00:15:33,330 --> 00:15:35,300 is where the environment comes in. 248 00:15:35,300 --> 00:15:43,710 It is a vacuum state, and here, this 249 00:15:43,710 --> 00:15:46,030 is the output part for the environment. 250 00:15:46,030 --> 00:15:49,110 This is where we do the measurement. 251 00:15:49,110 --> 00:15:53,880 And I don't think it matters. 252 00:15:53,880 --> 00:15:56,010 I haven't really told you which is mode A, which 253 00:15:56,010 --> 00:15:58,770 is mode B. It doesn't matter, but one, let's say 254 00:15:58,770 --> 00:16:01,650 the environment is mode B, and the system 255 00:16:01,650 --> 00:16:18,260 evolves in mode A. As you can see, 256 00:16:18,260 --> 00:16:20,110 I'm using a new program, which has 257 00:16:20,110 --> 00:16:22,620 some nicer features in terms of handwriting, 258 00:16:22,620 --> 00:16:26,770 but it is a little bit rough in scrolling, 259 00:16:26,770 --> 00:16:30,850 so I sometimes have to scroll back and forth. 260 00:16:30,850 --> 00:16:34,500 So what is our output? 261 00:16:34,500 --> 00:16:36,770 Now, we have two possibilities. 262 00:16:36,770 --> 00:16:40,382 The environment is 0, or the environment is 1, 263 00:16:40,382 --> 00:16:41,590 and we perform a measurement. 264 00:16:45,610 --> 00:16:50,120 So we have to now go into a probabilistic description. 265 00:16:50,120 --> 00:16:55,570 So with probability P1, we have done a measurement, 266 00:16:55,570 --> 00:17:04,700 and our output state is now the vacuum state. 267 00:17:04,700 --> 00:17:20,050 With probability 1 minus P1, we have not 268 00:17:20,050 --> 00:17:24,609 detected anything in the vacuum, and therefore, our state 269 00:17:24,609 --> 00:17:29,200 of the system is alpha 0 plus beta cosine theta 1. 270 00:17:36,530 --> 00:17:46,350 Is alpha 0, so it is not beta 1 as naively would have assumed. 271 00:17:46,350 --> 00:17:48,080 It's not the original state. 272 00:17:48,080 --> 00:17:52,060 There is a cosine theta factor, which we got exactly 273 00:17:52,060 --> 00:17:55,940 from the beam splitter from the unitary evolution provided 274 00:17:55,940 --> 00:17:58,130 by the beam splitter. 275 00:17:58,130 --> 00:18:01,660 And since these state is no longer normalized, 276 00:18:01,660 --> 00:18:07,210 I have to normalize it by alpha squared 277 00:18:07,210 --> 00:18:13,250 plus beta square cosine square theta. 278 00:18:13,250 --> 00:18:17,150 So now we have done our measurement probability P1 279 00:18:17,150 --> 00:18:18,430 to detect the photon. 280 00:18:18,430 --> 00:18:22,020 This projects the system into the vacuum state 281 00:18:22,020 --> 00:18:24,150 with the probability 1 minus P1. 282 00:18:24,150 --> 00:18:25,500 We have that state. 283 00:18:25,500 --> 00:18:26,370 Just one second. 284 00:18:26,370 --> 00:18:27,570 Scroll in the pictures. 285 00:18:30,330 --> 00:18:32,040 Write that down. 286 00:18:32,040 --> 00:18:36,140 In fact, millions that our system is now 287 00:18:36,140 --> 00:18:43,200 described by a density matrix with probability P1 288 00:18:43,200 --> 00:18:44,890 and 1 minus 1 minus P1. 289 00:18:48,810 --> 00:18:57,100 With probability P1, we are in the vacuum state, 290 00:18:57,100 --> 00:18:59,920 and with probability 1 minus P1, we 291 00:18:59,920 --> 00:19:04,640 are in that state, the denormalized state psi 292 00:19:04,640 --> 00:19:07,360 naught, which I just hold down. 293 00:19:07,360 --> 00:19:08,870 Question? 294 00:19:08,870 --> 00:19:10,680 AUDIENCE: Have you considered theta 295 00:19:10,680 --> 00:19:15,784 to be some like a dynamical phase evolution system. 296 00:19:15,784 --> 00:19:18,760 It's very low order like when you expand it 297 00:19:18,760 --> 00:19:21,240 the first time it looks almost identical to [INAUDIBLE] 298 00:19:21,240 --> 00:19:23,224 quantum effect maybe. 299 00:19:23,224 --> 00:19:28,860 The environment is measuring the state in some way, and I mean, 300 00:19:28,860 --> 00:19:30,120 it's the lowest order now. 301 00:19:30,120 --> 00:19:32,286 PROFESSOR: Yeah, I Quite agree that random 0 is just 302 00:19:32,286 --> 00:19:33,110 an example of it. 303 00:19:35,809 --> 00:19:37,100 Pretty much, it's all the same. 304 00:19:37,100 --> 00:19:38,550 Yeah. 305 00:19:38,550 --> 00:19:41,840 What we do here is, I like the beam splitter 306 00:19:41,840 --> 00:19:44,695 because the beam splitter provides an exact formulation 307 00:19:44,695 --> 00:19:46,190 of the measurement process. 308 00:19:46,190 --> 00:19:47,780 You really can use a beam splitter 309 00:19:47,780 --> 00:19:50,440 to discuss what happens fundamentally 310 00:19:50,440 --> 00:19:52,450 when you perform a measurement. 311 00:19:52,450 --> 00:19:56,570 And the beams splitter is one typical implementation of that, 312 00:19:56,570 --> 00:19:58,000 but it has all the features you'll 313 00:19:58,000 --> 00:19:59,291 find in any measurement system. 314 00:20:02,120 --> 00:20:04,350 And especially what you observe here, 315 00:20:04,350 --> 00:20:07,470 let me just emphasizes is, the fact that we you do not 316 00:20:07,470 --> 00:20:09,970 make a measurement is changing the way 317 00:20:09,970 --> 00:20:14,910 function from the initial wave function psi to psi naught, 318 00:20:14,910 --> 00:20:18,760 we have a factor of cosine theta here. 319 00:20:18,760 --> 00:20:21,170 And that's also very general. 320 00:20:21,170 --> 00:20:27,289 A measurement perturbs, modifies your wave function 321 00:20:27,289 --> 00:20:29,330 no matter what the outcome of the measurement is. 322 00:20:38,330 --> 00:20:41,460 So let me write it down because we 323 00:20:41,460 --> 00:20:45,400 want to take it to the next level. 324 00:20:45,400 --> 00:20:52,830 So we have now found in terms of the beam splitter, angle theta, 325 00:20:52,830 --> 00:20:59,070 and the parameters of the initial state, alpha beta. 326 00:20:59,070 --> 00:21:01,610 We found the density matrix after the beam splitter. 327 00:21:10,760 --> 00:21:12,920 Yes. 328 00:21:12,920 --> 00:21:15,000 So what is the next step? 329 00:21:15,000 --> 00:21:21,250 Our goal is to derive the master equation for the density 330 00:21:21,250 --> 00:21:24,100 matrix, the time evolution of the density matrix. 331 00:21:24,100 --> 00:21:27,950 So since we want to discuss the time evolution, 332 00:21:27,950 --> 00:21:30,620 we want to find a differential equation. 333 00:21:30,620 --> 00:21:32,260 So what we want to figure out is, 334 00:21:32,260 --> 00:21:36,710 what is the difference between the output density 335 00:21:36,710 --> 00:21:39,720 matrix and the input density matrix. 336 00:21:39,720 --> 00:21:42,730 The input was, of course, pure state 337 00:21:42,730 --> 00:21:48,130 characterized by the matrix population alpha squared 338 00:21:48,130 --> 00:21:54,170 and beta squared of diagonal matrix element of alpha beta. 339 00:22:03,810 --> 00:22:06,030 The difference between the density matrix 340 00:22:06,030 --> 00:22:08,660 is can just calculate the difference. 341 00:22:12,920 --> 00:22:19,640 You can simplify things by applying 342 00:22:19,640 --> 00:22:23,760 some trigonometric identities, so this 343 00:22:23,760 --> 00:22:40,710 is an exact result, cosine theta minus 1. 344 00:22:40,710 --> 00:22:48,450 Here we have alpha beta cosine theta minus 1, 345 00:22:48,450 --> 00:22:53,850 and on the diagonal, we have cosine 346 00:22:53,850 --> 00:22:58,870 2 theta minus 1 divided by 2. 347 00:22:58,870 --> 00:23:02,530 Anyway this is an intermediate result. 348 00:23:02,530 --> 00:23:04,760 We're interested in the differential equation. 349 00:23:04,760 --> 00:23:07,610 We want to sort of find out what happens when we observe, 350 00:23:07,610 --> 00:23:11,190 when we have the density matrix interacting 351 00:23:11,190 --> 00:23:13,600 with the environment all the time. 352 00:23:13,600 --> 00:23:17,850 And this can be simulated by beam splitters 353 00:23:17,850 --> 00:23:22,220 by using many beam splitters with a small degree 354 00:23:22,220 --> 00:23:24,650 of reflection. 355 00:23:24,650 --> 00:23:28,810 So we want to simplify this result now 356 00:23:28,810 --> 00:23:33,550 for the case of many beam splitters, and each of them 357 00:23:33,550 --> 00:23:44,040 has a small tipping angle, theta, 358 00:23:44,040 --> 00:23:53,620 and for later convenience, I defined theta to be gamma times 359 00:23:53,620 --> 00:23:55,460 delta t over 2. 360 00:23:55,460 --> 00:23:59,390 That's just my definition of theta. 361 00:23:59,390 --> 00:24:07,510 So what we have in mind now is that we start with the system 362 00:24:07,510 --> 00:24:15,230 psi, and we have many such beam splitters with an infinitesimal 363 00:24:15,230 --> 00:24:15,840 tipping angle. 364 00:24:21,250 --> 00:24:29,160 Each beam splitter has the vacuum at its input state. 365 00:24:32,620 --> 00:24:38,023 And we always perform the measurement. 366 00:24:48,390 --> 00:24:51,320 If I take the equation above, which 367 00:24:51,320 --> 00:24:55,740 I know you can't see anymore, we find a differential equation 368 00:24:55,740 --> 00:25:05,740 for the density matrix, which is we find an infinitesimal change 369 00:25:05,740 --> 00:25:11,390 delta over the density matrix, which looks like this. 370 00:25:19,650 --> 00:25:24,480 So all I've done is, I've used the equation above, 371 00:25:24,480 --> 00:25:30,120 and I've done a Taylor expansion in the small angle theta. 372 00:25:30,120 --> 00:25:32,820 And the reason why I brought in the square root, well, 373 00:25:32,820 --> 00:25:34,630 we get cosine theta. 374 00:25:34,630 --> 00:25:37,430 The first order Taylor expansion or the lowest order Taylor 375 00:25:37,430 --> 00:25:41,020 expansion from cosine is 1 minus theta squared. 376 00:25:41,020 --> 00:25:44,630 So I get the square root squared. 377 00:25:44,630 --> 00:25:46,610 So I get gamma, which appears here, 378 00:25:46,610 --> 00:25:49,240 and then I divide by delta t. 379 00:25:49,240 --> 00:25:52,800 So this is just an exact mathematical expression, 380 00:25:52,800 --> 00:26:00,350 and the next step is to form a differential equation. 381 00:26:00,350 --> 00:26:04,830 But before I do that, I want to emphasize the two features 382 00:26:04,830 --> 00:26:06,520 we are using here. 383 00:26:06,520 --> 00:26:08,140 They sort of enter automatically, 384 00:26:08,140 --> 00:26:11,280 but these are the two big assumptions 385 00:26:11,280 --> 00:26:14,360 we make when we derive a master equation. 386 00:26:14,360 --> 00:26:25,850 The first one is that we always have a vacuum state 387 00:26:25,850 --> 00:26:27,820 as the input. 388 00:26:27,820 --> 00:26:35,460 So in other words, the environment 389 00:26:35,460 --> 00:26:43,900 is always in the same state, which is a vacuum state, 390 00:26:43,900 --> 00:26:48,860 and this is sort of called a Bohr approximation. 391 00:26:48,860 --> 00:26:53,700 What it means is that we do a measurement here, 392 00:26:53,700 --> 00:26:55,860 but the vacuum is not changing. 393 00:26:55,860 --> 00:26:58,600 In other words, we are not overloading the vacuum 394 00:26:58,600 --> 00:27:02,830 with so many photons that suddenly the vacuum 395 00:27:02,830 --> 00:27:04,760 Is no longer in the vacuum state. 396 00:27:04,760 --> 00:27:06,770 Or in the case of spontaneous emission, 397 00:27:06,770 --> 00:27:10,500 the vacuum can just take as many photons as you dumping into it. 398 00:27:10,500 --> 00:27:14,120 They disappear so quickly that for all practical purposes, 399 00:27:14,120 --> 00:27:18,380 the environment stays in the vacuum state. 400 00:27:18,380 --> 00:27:20,300 So this is called the Bohr approximation. 401 00:27:20,300 --> 00:27:22,390 The environment is not changing. 402 00:27:22,390 --> 00:27:25,851 It has enough capacity you to be modified by the measurement 403 00:27:25,851 --> 00:27:26,350 process. 404 00:27:29,820 --> 00:27:42,260 And the second thing which is related 405 00:27:42,260 --> 00:27:49,540 is, the vacuum is always in the same state, 406 00:27:49,540 --> 00:27:56,120 and there are no correlations from here to here to here, 407 00:27:56,120 --> 00:27:57,990 there is no memory effect. 408 00:27:57,990 --> 00:27:59,690 Everything is completely uncorrelated. 409 00:28:07,340 --> 00:28:10,240 So the environment is uncorrelated. 410 00:28:13,990 --> 00:28:16,380 It has no memory. 411 00:28:16,380 --> 00:28:20,100 It's correlation function is a delta function, 412 00:28:20,100 --> 00:28:21,985 and this is called Markov approximation. 413 00:28:28,390 --> 00:28:31,040 So these are the two effects which are important. 414 00:28:31,040 --> 00:28:33,820 One is no memory for the environment, 415 00:28:33,820 --> 00:28:37,020 Delta function correlation, Markov approximation, 416 00:28:37,020 --> 00:28:40,290 and the two, of course, are related 417 00:28:40,290 --> 00:28:42,680 in the environment is all of this in the same state. 418 00:28:46,920 --> 00:28:59,100 So remember this is a change for the density matrix, 419 00:28:59,100 --> 00:29:03,480 and alpha beta where the original parameters 420 00:29:03,480 --> 00:29:06,460 of the density matrix for the input state. 421 00:29:06,460 --> 00:29:10,256 So I can now rewrite everything as a differential equation. 422 00:29:14,270 --> 00:29:19,130 The density matrix has a derivative 423 00:29:19,130 --> 00:29:26,370 for the diagonal matrix elements and for the coherences. 424 00:29:29,700 --> 00:29:33,700 Here we have plus gamma. 425 00:29:33,700 --> 00:29:36,950 Here we have minus gamma 0, 1, 1, 426 00:29:36,950 --> 00:29:40,640 makes sense because we conserve the trace. 427 00:29:40,640 --> 00:29:44,290 We have unity probability that we have a stellar system. 428 00:29:44,290 --> 00:29:47,830 And therefore the two diagonal matrix elements, 429 00:29:47,830 --> 00:29:52,160 the population, the sum of them cannot change with time. 430 00:29:54,970 --> 00:30:00,120 And for the coherence, we have gamma over 2. 431 00:30:03,340 --> 00:30:10,010 And if you're familiar with Optical Bloch Equations, which 432 00:30:10,010 --> 00:30:13,460 we derive next, we can say that these 433 00:30:13,460 --> 00:30:20,970 means if 0 is the ground state that the ground state changes 434 00:30:20,970 --> 00:30:25,050 because-- call it spontaneous emission from the excited 435 00:30:25,050 --> 00:30:26,480 state. 436 00:30:26,480 --> 00:30:30,940 This equation would say that the excited state decays 437 00:30:30,940 --> 00:30:35,620 with the rate gamma, and sometimes you 438 00:30:35,620 --> 00:30:38,430 may have wondered about that there are factors 439 00:30:38,430 --> 00:30:41,800 of two appearing, which also appears here 440 00:30:41,800 --> 00:30:46,790 that when the excited state decays with a rate gamma, 441 00:30:46,790 --> 00:30:49,310 we have a factor here for the coherences, which 442 00:30:49,310 --> 00:30:50,380 is gamma over 2. 443 00:30:53,800 --> 00:30:56,950 So what we have accomplished in contrast 444 00:30:56,950 --> 00:31:00,430 to let's say Einstein's equation with the Einstein 445 00:31:00,430 --> 00:31:03,500 a and b coefficient, which lead to rate 446 00:31:03,500 --> 00:31:10,080 equations for the population, we have now a new feature. 447 00:31:10,080 --> 00:31:14,450 We have an the equation for the coherences, 448 00:31:14,450 --> 00:31:17,685 and we find a decay of the coherences 449 00:31:17,685 --> 00:31:20,535 with half the rate as a decay of the population. 450 00:31:24,921 --> 00:31:25,420 Questions? 451 00:31:36,190 --> 00:31:41,400 So if you want you could rewrite this model for photon, which 452 00:31:41,400 --> 00:31:44,180 goes through beam splitters, undergoes measurement. 453 00:31:44,180 --> 00:31:46,840 You can rewrite it from atomic wave function 454 00:31:46,840 --> 00:31:48,620 and you measure whether the atomics 455 00:31:48,620 --> 00:31:52,390 in the excited and ground state and the equation 456 00:31:52,390 --> 00:31:54,490 for the measurement performed on the atom 457 00:31:54,490 --> 00:32:01,060 is exactly as the equation by which the beam splitter acts 458 00:32:01,060 --> 00:32:02,460 on the photon state. 459 00:32:02,460 --> 00:32:04,150 So what I've shown here it's very 460 00:32:04,150 --> 00:32:06,450 specific for a single photon because I 461 00:32:06,450 --> 00:32:09,000 could use simple equations, but everything 462 00:32:09,000 --> 00:32:14,535 is what you find in a much more general situation. 463 00:32:17,180 --> 00:32:23,100 So before I give you the general derivation of the master 464 00:32:23,100 --> 00:32:33,490 equation, let me talk about what we have learned 465 00:32:33,490 --> 00:32:41,080 from this example and what the general procedure is. 466 00:32:46,620 --> 00:32:53,650 The first thing is our goal is to find a differential 467 00:32:53,650 --> 00:32:58,760 equation for the density matrix of the system. 468 00:32:58,760 --> 00:32:59,690 I just remember. 469 00:32:59,690 --> 00:33:02,940 There was one thing I wanted to mention. 470 00:33:02,940 --> 00:33:05,370 In the previous derivation with the beam splitter, 471 00:33:05,370 --> 00:33:09,250 I started with a purer state, and the purer state 472 00:33:09,250 --> 00:33:11,930 developed into a statistical mixture, 473 00:33:11,930 --> 00:33:14,350 and this statistical mixture would then 474 00:33:14,350 --> 00:33:16,490 transform the next beam splitter into 475 00:33:16,490 --> 00:33:18,610 another statistical mixture. 476 00:33:18,610 --> 00:33:21,550 I derived the differential equation for you 477 00:33:21,550 --> 00:33:23,530 for the first state from the pure state 478 00:33:23,530 --> 00:33:25,340 to the statistical mixture. 479 00:33:25,340 --> 00:33:27,210 But if you would spend a few minutes, 480 00:33:27,210 --> 00:33:29,100 you could immediately show that you 481 00:33:29,100 --> 00:33:31,950 can start with an elementary density matrix, 482 00:33:31,950 --> 00:33:34,300 look how it evolves through the beam splitter, 483 00:33:34,300 --> 00:33:38,750 and you get exactly the same differential equation. 484 00:33:46,380 --> 00:33:52,260 So the general procedure is, we want a differential equation 485 00:33:52,260 --> 00:33:57,490 how the density matrix evolves with time. 486 00:33:57,490 --> 00:34:03,360 And this will be obtained by finding an operator which 487 00:34:03,360 --> 00:34:05,925 acts on the initial density matrix. 488 00:34:08,730 --> 00:34:11,949 This operator is not a unitary operator 489 00:34:11,949 --> 00:34:14,100 because we are performing measurements 490 00:34:14,100 --> 00:34:16,530 through the environment, even if you don't actually 491 00:34:16,530 --> 00:34:17,750 perform them. 492 00:34:17,750 --> 00:34:20,429 Once we dump something into the environment, 493 00:34:20,429 --> 00:34:22,750 it's out of our control and anybody 494 00:34:22,750 --> 00:34:25,260 could go and perform a measurement, 495 00:34:25,260 --> 00:34:27,330 and so we should assume that this measurement has 496 00:34:27,330 --> 00:34:27,790 been taken. 497 00:34:27,790 --> 00:34:29,581 It's one of those quantum mechanical things 498 00:34:29,581 --> 00:34:32,380 that you don't even have to care whether somebody does it. 499 00:34:32,380 --> 00:34:35,790 The environment does it for you. 500 00:34:35,790 --> 00:34:42,699 So this operator is called a Liouvillian operator. 501 00:34:45,850 --> 00:34:48,120 It's sometimes called-- and I haven't really 502 00:34:48,120 --> 00:34:51,389 traced down why-- it's called sometimes super operator. 503 00:34:55,830 --> 00:34:57,730 I know what superconductivity is, 504 00:34:57,730 --> 00:35:01,070 but I don't know what the super powers of this operator are, 505 00:35:01,070 --> 00:35:06,080 but that's just a name which you will find. 506 00:35:06,080 --> 00:35:08,010 The second thing which we have used 507 00:35:08,010 --> 00:35:14,390 is that the evolution of this system 508 00:35:14,390 --> 00:35:23,050 can be obtained from the time evolution of the total system 509 00:35:23,050 --> 00:35:28,430 by performing a trace over the degrees of freedom 510 00:35:28,430 --> 00:35:29,870 of the environment. 511 00:35:29,870 --> 00:35:31,750 This was exactly what we actually 512 00:35:31,750 --> 00:35:36,070 did when we said the system continues with probability P 513 00:35:36,070 --> 00:35:38,480 naught in one state and probability 514 00:35:38,480 --> 00:35:39,810 P1 in the other state. 515 00:35:39,810 --> 00:35:42,620 The operation which lead to this density matrix 516 00:35:42,620 --> 00:35:44,060 was exactly the partial trace. 517 00:35:49,820 --> 00:35:57,385 So this is the second general feature 518 00:35:57,385 --> 00:36:00,630 which we have to implement. 519 00:36:00,630 --> 00:36:05,510 Thirdly, if we could do one and two exactly, 520 00:36:05,510 --> 00:36:07,100 we would have an exact formulation 521 00:36:07,100 --> 00:36:10,220 for a small part of a quantum system 522 00:36:10,220 --> 00:36:13,030 no matter how complicated the environment is. 523 00:36:13,030 --> 00:36:17,800 In practice, we can solve the equations only 524 00:36:17,800 --> 00:36:22,350 when we make simplifying assumptions 525 00:36:22,350 --> 00:36:23,740 about the environment. 526 00:36:27,870 --> 00:36:34,350 One is, it is large, and more important, 527 00:36:34,350 --> 00:36:42,010 therefore, it's unchanging, and this is the Bohr approximation. 528 00:36:42,010 --> 00:36:47,080 And the second feature is, it has a short correlation 529 00:36:47,080 --> 00:36:55,690 time, tau c. 530 00:36:55,690 --> 00:36:58,160 In the beam splitter, I have made the assumption 531 00:36:58,160 --> 00:37:00,490 that there is no correlation between different beam 532 00:37:00,490 --> 00:37:02,460 splitters in the derivation, which 533 00:37:02,460 --> 00:37:04,240 I want to walk you through. 534 00:37:04,240 --> 00:37:09,130 Right now, you will see explicitly 535 00:37:09,130 --> 00:37:11,170 where the correlation times enter. 536 00:37:11,170 --> 00:37:13,355 And this is called the Markov approximation. 537 00:37:18,910 --> 00:37:26,920 And finally, this is number four, the whole possibility 538 00:37:26,920 --> 00:37:33,850 to derive a master equation hinges on the fact 539 00:37:33,850 --> 00:37:37,780 that we have different time scales which 540 00:37:37,780 --> 00:37:39,120 are very different. 541 00:37:48,490 --> 00:37:58,100 We are interested in the evolution of our system. 542 00:37:58,100 --> 00:38:02,680 We want to know how it relaxes, and this is on a time scale 543 00:38:02,680 --> 00:38:03,700 1 over gamma. 544 00:38:06,240 --> 00:38:08,670 So we call this slow. 545 00:38:08,670 --> 00:38:13,130 We are interested in the variation 546 00:38:13,130 --> 00:38:18,100 of our system, the atomic system or the photon state, 547 00:38:18,100 --> 00:38:21,510 which passes through the beam splitter, 548 00:38:21,510 --> 00:38:25,270 and this time scale has to be much slower 549 00:38:25,270 --> 00:38:27,600 than the fluctuations of the environment. 550 00:38:35,550 --> 00:38:45,440 So therefore, if the environment has fluctuations, 551 00:38:45,440 --> 00:38:47,110 which in the beam splitter model where 552 00:38:47,110 --> 00:38:50,510 assumed to be 0, it was delta function of time, 553 00:38:50,510 --> 00:38:55,880 if that correlation time is much smaller than the time 554 00:38:55,880 --> 00:39:00,480 it takes for the system to relax and to evolve, 555 00:39:00,480 --> 00:39:06,300 that opens a window delta t, and this 556 00:39:06,300 --> 00:39:09,370 is the time scale of the master equation. 557 00:39:16,610 --> 00:39:19,650 Just to give you one example for the spontaneous emission, 558 00:39:19,650 --> 00:39:22,910 the correlation time, tau c, would 559 00:39:22,910 --> 00:39:27,920 be the time it takes the photon to disappear from the atom. 560 00:39:27,920 --> 00:39:30,610 And the photon has disappeared from the atom 561 00:39:30,610 --> 00:39:33,140 when it is one wavelengths away. 562 00:39:33,140 --> 00:39:35,490 So typically, the correlation time 563 00:39:35,490 --> 00:39:38,330 f the vacuum for spontaneous emission 564 00:39:38,330 --> 00:39:44,070 is one cycle of the optical frequency. 565 00:39:44,070 --> 00:39:45,840 It's very, very fast. 566 00:39:45,840 --> 00:39:50,490 Whereas typical decay times of the excited states, 567 00:39:50,490 --> 00:39:51,180 a nano second. 568 00:39:51,180 --> 00:39:53,400 It's six orders of magnitude slower, 569 00:39:53,400 --> 00:39:56,160 and this is what we describe. 570 00:39:56,160 --> 00:39:58,892 But on a time scale of a femtosecond 571 00:39:58,892 --> 00:40:04,460 of one optical cycle, the photon has not detached from the atom 572 00:40:04,460 --> 00:40:06,980 and it could go actually back to the atom. 573 00:40:06,980 --> 00:40:11,440 During that time, we talked a little bit about it 574 00:40:11,440 --> 00:40:14,770 when we did this diagrammatic discussions of resonance 575 00:40:14,770 --> 00:40:17,090 scattering for very, very early times. 576 00:40:17,090 --> 00:40:21,130 You don't have exponential decay because you cannot do 577 00:40:21,130 --> 00:40:24,130 the approximations where we approximated the kernel 578 00:40:24,130 --> 00:40:26,860 by something which was completely energy dependent. 579 00:40:26,860 --> 00:40:30,030 And so what happens at such short times, 580 00:40:30,030 --> 00:40:32,994 we encounter here again in such short times, 581 00:40:32,994 --> 00:40:35,160 we will not have a simple description of the system. 582 00:40:47,200 --> 00:40:50,120 So the last point, let me summarize. 583 00:40:50,120 --> 00:40:57,310 Our goal is that we describe the density matrix of the system, 584 00:40:57,310 --> 00:41:00,420 and we want to find the Liouville operator 585 00:41:00,420 --> 00:41:04,470 or some matrix which acts on it. 586 00:41:04,470 --> 00:41:11,490 And because we will integrate over time steps, which 587 00:41:11,490 --> 00:41:14,910 are larger than the correlation time of the system, 588 00:41:14,910 --> 00:41:21,520 we can also call it, it will be a coarse-grained evolution. 589 00:41:28,810 --> 00:41:30,400 Any questions about that? 590 00:41:44,640 --> 00:41:48,550 I really like the discussion, the derivation of the master 591 00:41:48,550 --> 00:41:53,490 equation, how it is presented in atom-photon indirection. 592 00:41:53,490 --> 00:41:57,230 But it is presented on more than 50 pages 593 00:41:57,230 --> 00:41:59,470 with many, many equations. 594 00:41:59,470 --> 00:42:02,640 So after giving you all of the principles, all 595 00:42:02,640 --> 00:42:06,030 of the concepts, I want to go with you now 596 00:42:06,030 --> 00:42:09,820 over those equations and point out how 597 00:42:09,820 --> 00:42:13,430 the principles, which we encountered with the beam 598 00:42:13,430 --> 00:42:16,120 splitter, how they are now implemented 599 00:42:16,120 --> 00:42:18,520 in a very general context. 600 00:42:18,520 --> 00:42:23,890 I will not be able to give you all of the mathematical aspects 601 00:42:23,890 --> 00:42:27,920 of it, but I think by now you know that the book atom-photon 602 00:42:27,920 --> 00:42:29,660 interactions are actually wonderful. 603 00:42:29,660 --> 00:42:33,400 You can get a lot of conception information out of it 604 00:42:33,400 --> 00:42:37,150 by looking at the equations without understanding 605 00:42:37,150 --> 00:42:38,830 every technical detail. 606 00:42:38,830 --> 00:42:42,670 So I would really encourage you, if there is something which 607 00:42:42,670 --> 00:42:45,800 piques your interest and I hope there will be things which 608 00:42:45,800 --> 00:42:48,840 you'll find very interesting, that you go to the book 609 00:42:48,840 --> 00:42:50,070 and read it. 610 00:42:50,070 --> 00:42:51,950 So I'm exactly following that actually I 611 00:42:51,950 --> 00:42:53,960 used copies of the book. 612 00:42:53,960 --> 00:42:58,550 So we have a Hamiltonian, which is 613 00:42:58,550 --> 00:43:01,730 describing the atomic system. 614 00:43:01,730 --> 00:43:06,521 It describes the reservoir and then there is an interaction. 615 00:43:06,521 --> 00:43:09,020 We keep it very general here, but you may always think well, 616 00:43:09,020 --> 00:43:13,340 the atom is your favorite two-level system. 617 00:43:13,340 --> 00:43:16,350 The environment is maybe the vacuum 618 00:43:16,350 --> 00:43:19,030 with all its possible modes, and the interaction 619 00:43:19,030 --> 00:43:22,670 is the dipole interaction or the a dot p interaction. 620 00:43:33,290 --> 00:43:41,060 So we start out with an equation, 621 00:43:41,060 --> 00:43:46,630 which is nothing else than Schrodinger's 622 00:43:46,630 --> 00:43:52,400 equation for the density matrix. 623 00:43:52,400 --> 00:43:54,360 The time derivation of the density matrix 624 00:43:54,360 --> 00:43:57,670 is commutative with the Hamilton. 625 00:43:57,670 --> 00:44:01,320 But it is often useful and you've seen it many times, 626 00:44:01,320 --> 00:44:03,880 to go to the interaction representation, 627 00:44:03,880 --> 00:44:08,370 that the time dependence due to the unperturbed part 628 00:44:08,370 --> 00:44:12,810 of the operator is absorbed in a unitary transformation, 629 00:44:12,810 --> 00:44:16,850 so therefore, this density matrix in the interaction 630 00:44:16,850 --> 00:44:22,030 representation evolves not with, h, because h naught is taken 631 00:44:22,030 --> 00:44:25,396 care of, it only involves due to the coupling between the two 632 00:44:25,396 --> 00:44:27,395 systems, between the system and the environment. 633 00:44:35,220 --> 00:44:38,580 So now this equation, we are interested in a time step delta 634 00:44:38,580 --> 00:44:40,000 t. 635 00:44:40,000 --> 00:44:42,700 And this time step, delta t remember, 636 00:44:42,700 --> 00:44:45,040 we want to coarse grain, will be larger 637 00:44:45,040 --> 00:44:47,230 than the correlation time of the reservoir, 638 00:44:47,230 --> 00:44:49,660 and you will see exactly where it comes about. 639 00:44:49,660 --> 00:44:53,390 So we want to now do one of those coarse-grain steps. 640 00:44:53,390 --> 00:44:57,180 We take this equation and we integrate from time t 641 00:44:57,180 --> 00:44:58,580 to time t plus delta t. 642 00:45:01,260 --> 00:45:04,560 So this is exact here. 643 00:45:07,750 --> 00:45:19,815 But now we want to iterate, and that means the following. 644 00:45:22,640 --> 00:45:26,750 We have expressed the time step in the density matrix 645 00:45:26,750 --> 00:45:29,570 by having the density matrix there. 646 00:45:29,570 --> 00:45:36,080 But now we can do in a first-order perturbation 647 00:45:36,080 --> 00:45:40,260 theory, we can do one step and we get the second order result 648 00:45:40,260 --> 00:45:43,640 by plugging the first order result into this equation. 649 00:45:43,640 --> 00:45:46,490 It's the same we have seen with our diagrams and such. 650 00:45:46,490 --> 00:45:49,950 We have an exact equation. 651 00:45:49,950 --> 00:45:53,090 It's useless unless we do something, and what we do is, 652 00:45:53,090 --> 00:45:56,630 we realize that we can iterate it 653 00:45:56,630 --> 00:46:00,630 because the part we don't know involves one more 654 00:46:00,630 --> 00:46:02,840 occurrence of the interaction potential. 655 00:46:02,840 --> 00:46:05,740 And when you plug the nth order solution in here, 656 00:46:05,740 --> 00:46:07,647 you get the n plus first order solution. 657 00:46:07,647 --> 00:46:09,230 And this is exactly what is done here. 658 00:46:15,810 --> 00:46:18,370 And I skipped a few equations here. 659 00:46:18,370 --> 00:46:20,990 This is what he's done here, number one. 660 00:46:20,990 --> 00:46:24,160 And number two is, we are interested in the system, 661 00:46:24,160 --> 00:46:26,380 not in the reservoir, so therefore we 662 00:46:26,380 --> 00:46:29,910 perform the trace over the reservoir. 663 00:46:29,910 --> 00:46:32,920 And the trace of the reservoir for the photon beam splitter 664 00:46:32,920 --> 00:46:38,370 mend, we say we have two possible states, 665 00:46:38,370 --> 00:46:40,240 we detect a photon or not. 666 00:46:40,240 --> 00:46:43,540 And for the system, we have now a density matrix 667 00:46:43,540 --> 00:46:47,680 which is probability P naught in one state, probability 668 00:46:47,680 --> 00:46:49,750 P1 in the other state. 669 00:46:49,750 --> 00:46:54,590 And this is exactly what the operator partial trace does. 670 00:46:54,590 --> 00:46:57,030 Remember also I want to really make sure 671 00:46:57,030 --> 00:46:59,190 that you recognize all the structures. 672 00:46:59,190 --> 00:47:04,550 The time evolution of a density matrix was a commutator with h, 673 00:47:04,550 --> 00:47:08,350 but in the interaction picture, it's a commutator with v. 674 00:47:08,350 --> 00:47:13,010 But since we are putting the first order result in here, 675 00:47:13,010 --> 00:47:16,610 the second order result is now the commutator 676 00:47:16,610 --> 00:47:19,910 of v with the commutator of v and o. 677 00:47:19,910 --> 00:47:22,430 It's just we have iterated one more time. 678 00:47:30,240 --> 00:47:40,290 So the sigma tilde, the density matrix for our system, 679 00:47:40,290 --> 00:47:43,470 tilde means in the interaction picture 680 00:47:43,470 --> 00:47:48,180 is now the partial trace over the reservoir 681 00:47:48,180 --> 00:47:50,570 of the total density matrix. 682 00:47:50,570 --> 00:47:52,630 Tilde means in the interaction picture. 683 00:47:55,380 --> 00:48:01,840 And the important part here is that it is exact. 684 00:48:01,840 --> 00:48:06,982 We have not done any approximation here. 685 00:48:06,982 --> 00:48:07,565 Any questions? 686 00:48:24,840 --> 00:48:28,510 Of course, now we have to make approximations because we 687 00:48:28,510 --> 00:48:31,870 cannot solve an interactive problem exactly. 688 00:48:31,870 --> 00:48:37,080 The first one is-- and what do we want to do in the end? 689 00:48:37,080 --> 00:48:41,790 We want to keep the first non-trivial term 690 00:48:41,790 --> 00:48:44,910 but to the extent possible, we want to factorize everything. 691 00:48:44,910 --> 00:48:47,490 We want to get rid of the entanglement of the environment 692 00:48:47,490 --> 00:48:51,260 in the system and only get sort of the minimum which 693 00:48:51,260 --> 00:48:53,370 is provided by the coupling. 694 00:48:53,370 --> 00:48:55,790 So this evolves as follows. 695 00:48:55,790 --> 00:49:01,640 The interaction we assume is a product of two operators. 696 00:49:01,640 --> 00:49:04,380 One operator acts on the system, one operator 697 00:49:04,380 --> 00:49:06,390 acts on the environment. 698 00:49:06,390 --> 00:49:10,115 So this could be the dipole acting on the atom, the vacuum 699 00:49:10,115 --> 00:49:13,730 field, e, interacting with the environment 700 00:49:13,730 --> 00:49:16,160 or it could be p dot a. 701 00:49:16,160 --> 00:49:20,440 Or maybe your system has a magnetic moment, m, 702 00:49:20,440 --> 00:49:25,870 and the environment consists of fluctuating magnetic fields. 703 00:49:25,870 --> 00:49:29,382 So we'll pretty much find in every kind of measurement 704 00:49:29,382 --> 00:49:33,460 that a measurement involves the product of two operators. 705 00:49:33,460 --> 00:49:36,700 One is an operator for your system 706 00:49:36,700 --> 00:49:39,200 and one is an operator for the reservoir of the environment. 707 00:49:44,280 --> 00:49:50,600 And so this is one thing we want to use, 708 00:49:50,600 --> 00:49:53,700 and now there is one thing which the moment we 709 00:49:53,700 --> 00:49:57,390 will set in our equations, there is one thing 710 00:49:57,390 --> 00:50:01,560 which will naturally appear. 711 00:50:01,560 --> 00:50:03,414 Let me scroll back. 712 00:50:07,130 --> 00:50:10,520 What we have here is the interaction operator, v, 713 00:50:10,520 --> 00:50:13,240 at two different times. 714 00:50:13,240 --> 00:50:16,410 So this means if something happens at different times 715 00:50:16,410 --> 00:50:18,150 and we integrate over times. 716 00:50:18,150 --> 00:50:21,000 This is a correlation function, a correlation function 717 00:50:21,000 --> 00:50:26,360 between v at the time t prime and the time t double prime 718 00:50:26,360 --> 00:50:33,450 and since the reservoir part of this interaction 719 00:50:33,450 --> 00:50:37,690 is the operator, r, so what we have here now is, 720 00:50:37,690 --> 00:50:41,650 we have a correlation between the operator, r, 721 00:50:41,650 --> 00:50:46,220 at two times, which characterizes the environment. 722 00:50:46,220 --> 00:50:48,690 And now comes an important approximation. 723 00:50:48,690 --> 00:50:54,630 You remember I said we want to assume that the environment has 724 00:50:54,630 --> 00:50:56,600 a very short correlation time. 725 00:50:56,600 --> 00:51:01,150 Whenever a photon is emitted, it appears dramatically fast. 726 00:51:01,150 --> 00:51:03,470 It disappears in one optical cycle, 727 00:51:03,470 --> 00:51:05,220 and the environment is sort of reset, 728 00:51:05,220 --> 00:51:07,500 it's back in the vacuum state. 729 00:51:07,500 --> 00:51:11,100 So this is now expressed here that this product over which 730 00:51:11,100 --> 00:51:17,120 we take the partial trace has a very short coherence time. 731 00:51:17,120 --> 00:51:20,900 And the fact is now the following. 732 00:51:20,900 --> 00:51:29,380 We are integrating over a coarse-grained step delta t, 733 00:51:29,380 --> 00:51:33,910 but this correlation function goes to 0 in a very short time. 734 00:51:33,910 --> 00:51:39,810 So therefore it will not contribute a lot. 735 00:51:39,810 --> 00:51:40,900 Let me write that down. 736 00:51:54,000 --> 00:52:00,080 What we are going to approximate is our total density matrix 737 00:52:00,080 --> 00:52:08,870 is now approximately factorizing in a density matrix 738 00:52:08,870 --> 00:52:11,420 describing the atomic system. 739 00:52:11,420 --> 00:52:14,500 Well, we describe the atomic system 740 00:52:14,500 --> 00:52:17,570 when we trace out the environment. 741 00:52:17,570 --> 00:52:24,190 We describe the environment when we trace out the atomic part. 742 00:52:24,190 --> 00:52:26,820 And if we now form the direct product, 743 00:52:26,820 --> 00:52:28,990 we are back to the total system, but we 744 00:52:28,990 --> 00:52:32,500 have factorized the total density matrix into two parts. 745 00:52:35,360 --> 00:52:42,140 What we neglect here is a part which cannot be factorized 746 00:52:42,140 --> 00:52:44,700 which is the correlated part of it. 747 00:52:47,520 --> 00:52:52,390 But what happens is, since we are integrating over time steps 748 00:52:52,390 --> 00:52:55,790 delta t and the correlation decay 749 00:52:55,790 --> 00:53:00,920 in a very, very short time, the result is 750 00:53:00,920 --> 00:53:05,200 that this complicated part, which we could never calculate, 751 00:53:05,200 --> 00:53:12,230 is smaller than the first part by the ratio of the time 752 00:53:12,230 --> 00:53:16,590 where the correlations contribute over the time delta 753 00:53:16,590 --> 00:53:20,100 t, the time step we are going to take. 754 00:53:20,100 --> 00:53:23,720 So this is a very critical assumption. 755 00:53:23,720 --> 00:53:26,900 There is a whole page or two in the book where 756 00:53:26,900 --> 00:53:29,250 an photon-atom interaction they discuss 757 00:53:29,250 --> 00:53:34,270 the validity of this assumption, but I've given you 758 00:53:34,270 --> 00:53:38,810 the physical motivation that we indicate over much larger time, 759 00:53:38,810 --> 00:53:41,330 and if this time is large and the correlation is 760 00:53:41,330 --> 00:53:48,284 lost for short time, they only contribute 761 00:53:48,284 --> 00:53:49,950 with this small parameter to the result. 762 00:53:52,470 --> 00:53:56,950 So in other words, this means after-- we 763 00:53:56,950 --> 00:53:59,750 have an interaction between the environment and the system. 764 00:53:59,750 --> 00:54:01,690 We write it down in second order, 765 00:54:01,690 --> 00:54:07,080 but the second order result is now 766 00:54:07,080 --> 00:54:11,810 we evaluated by factorizing the density 767 00:54:11,810 --> 00:54:17,180 matrix into our system in the reservoir. 768 00:54:17,180 --> 00:54:19,810 So that means in that sense if you factorize something, 769 00:54:19,810 --> 00:54:21,550 it looks as if it's not interacting, 770 00:54:21,550 --> 00:54:23,050 but the trick is the same. 771 00:54:23,050 --> 00:54:25,870 You write down something to first and second order, 772 00:54:25,870 --> 00:54:29,190 and once you have factored out the important physics, 773 00:54:29,190 --> 00:54:31,820 now you can evaluate the expression 774 00:54:31,820 --> 00:54:36,760 by using an approximation, which is now the approximation 775 00:54:36,760 --> 00:54:38,910 that the density matrix factorizes. 776 00:54:51,850 --> 00:55:00,430 So with that, this is the approximation 777 00:55:00,430 --> 00:55:05,080 that we have made that the correlation time is very short. 778 00:55:05,080 --> 00:55:09,170 And now we have a differential equation 779 00:55:09,170 --> 00:55:11,870 for the density matrix sigma, which describes 780 00:55:11,870 --> 00:55:12,960 or atomic system. 781 00:55:18,612 --> 00:55:21,170 We have traced out the degrees of the reservoir. 782 00:55:24,120 --> 00:55:28,900 And now we want to insert B.17. 783 00:55:28,900 --> 00:55:31,000 You probably don't remember what B.17 is. 784 00:55:31,000 --> 00:55:32,950 It says that the interaction operator 785 00:55:32,950 --> 00:55:36,940 is a product of a, the operator a for the atoms 786 00:55:36,940 --> 00:55:40,130 and r for the reservoir. 787 00:55:40,130 --> 00:55:44,280 So the reservoir part, tau prime tau double prime, 788 00:55:44,280 --> 00:55:46,340 gives a correlation function. 789 00:55:46,340 --> 00:55:49,690 This is the correlation function between the operator, 790 00:55:49,690 --> 00:55:54,290 r, at two different times and the part 791 00:55:54,290 --> 00:55:59,009 which acts on our system, the a part, is explicitly kept here. 792 00:56:03,320 --> 00:56:07,510 So this is now a general master equation. 793 00:56:07,510 --> 00:56:10,200 It tells us the time evolution of the density 794 00:56:10,200 --> 00:56:16,270 matrix in this form. 795 00:56:16,270 --> 00:56:18,370 It looks very complicated, but this 796 00:56:18,370 --> 00:56:20,990 is because it's very general. 797 00:56:20,990 --> 00:56:31,600 In order to bring it into an easier form, 798 00:56:31,600 --> 00:56:38,590 we want to now introduce a basis of states, energy eigenstates 799 00:56:38,590 --> 00:56:41,960 of the unperturbed system, and write down 800 00:56:41,960 --> 00:56:45,920 all of these operator into such a basis of states. 801 00:56:48,960 --> 00:56:53,080 But anyway you saw here how we had an exact equation, 802 00:56:53,080 --> 00:56:57,120 and the main approximation we made 803 00:56:57,120 --> 00:57:01,680 is that the operator acting on the environment 804 00:57:01,680 --> 00:57:03,460 has a very short correlation time. 805 00:57:07,907 --> 00:57:08,490 Any questions? 806 00:57:11,676 --> 00:57:13,850 Well, you're only a few minutes away 807 00:57:13,850 --> 00:57:17,040 from producing this result to Fermi's golden rule, which 808 00:57:17,040 --> 00:57:18,810 you have known for a long, long time. 809 00:57:18,810 --> 00:57:21,350 It's just we have made very general assumptions. 810 00:57:21,350 --> 00:57:25,770 You see sort of how the assumptions propagate, 811 00:57:25,770 --> 00:57:31,730 but now if you write it down for an energy eigenbasis, 812 00:57:31,730 --> 00:57:35,550 you will immediately see results you have probably 813 00:57:35,550 --> 00:57:39,310 known since your childhood. 814 00:57:39,310 --> 00:57:41,330 So we want to have energy eigenstates 815 00:57:41,330 --> 00:57:42,940 of the atomic operators, so this is 816 00:57:42,940 --> 00:57:44,650 sort of ground and excited state if you 817 00:57:44,650 --> 00:57:48,060 think about a two-level system. 818 00:57:48,060 --> 00:57:53,100 The previous equation, I have to go back to it. 819 00:58:00,520 --> 00:58:04,130 Our previous equation is a differential equation 820 00:58:04,130 --> 00:58:08,730 for the density matrix here, and here is the density matrix. 821 00:58:08,730 --> 00:58:12,340 So now we formulate this equation 822 00:58:12,340 --> 00:58:16,230 into an energy eigenbasis, and what do we get? 823 00:58:16,230 --> 00:58:18,850 Well, we get an equation for the matrix elements, 824 00:58:18,850 --> 00:58:21,290 and what matrix elements are important? 825 00:58:21,290 --> 00:58:24,160 diagonal matrix elements which are population 826 00:58:24,160 --> 00:58:26,870 of diagonal matrix elements which are coherences. 827 00:58:26,870 --> 00:58:29,190 So we pretty much take this equation, 828 00:58:29,190 --> 00:58:31,800 use the energy eigenbasis and look, 829 00:58:31,800 --> 00:58:34,327 what do we get for the populations 830 00:58:34,327 --> 00:58:35,910 and what do we get for the coherences. 831 00:58:50,450 --> 00:58:57,140 So the structure is now the following. 832 00:58:57,140 --> 00:58:59,860 That we have our matrix elements ab. 833 00:59:03,780 --> 00:59:09,030 There is one part which looks like a unitary time evolution. 834 00:59:09,030 --> 00:59:11,180 This is what comes from the Hamilton operator. 835 00:59:11,180 --> 00:59:15,420 This is sort of the-- we'll see that in a moment-- 836 00:59:15,420 --> 00:59:19,020 but this is the time evolution without relaxation 837 00:59:19,020 --> 00:59:21,330 and now we have something here which 838 00:59:21,330 --> 00:59:24,650 are generalized relaxation coefficients. 839 00:59:24,650 --> 00:59:26,960 And you will find if you go further above 840 00:59:26,960 --> 00:59:29,450 that those relaxation coefficients are directly 841 00:59:29,450 --> 00:59:34,440 related to the correlation function of the reservoir. 842 00:59:34,440 --> 00:59:42,260 So we can now specify what happens between populations. 843 00:59:42,260 --> 00:59:45,580 Population means that we have a differential equation, 844 00:59:45,580 --> 00:59:48,770 let's say between sigma aa the puller, 845 00:59:48,770 --> 01:00:01,410 and sigma cc, so we have a rate coefficient 846 01:00:01,410 --> 01:00:04,900 which connects the population in state A 847 01:00:04,900 --> 01:00:10,370 with the population in state C. 848 01:00:10,370 --> 01:00:14,910 And if you take this expression, you find several things. 849 01:00:14,910 --> 01:00:18,180 Well, you find Fermi's golden rule, 850 01:00:18,180 --> 01:00:21,510 in a generalized way-- that's always 851 01:00:21,510 --> 01:00:25,590 nice-- you find Fermi's golden rule. 852 01:00:25,590 --> 01:00:29,530 When you integrate over time, you often get data function, 853 01:00:29,530 --> 01:00:32,200 and you expect to get a delta function because 854 01:00:32,200 --> 01:00:34,040 of energy conservation. 855 01:00:34,040 --> 01:00:36,710 So you get that, of course, naturally. 856 01:00:36,710 --> 01:00:42,040 Secondly, we have second order matrix element, 857 01:00:42,040 --> 01:00:44,920 which you know from Fermi's golden rule, 858 01:00:44,920 --> 01:00:47,710 but now we have the following situation 859 01:00:47,710 --> 01:00:51,770 that the matrix element in Fermi's golden rule 860 01:00:51,770 --> 01:00:57,190 may actually depend on the state, mu, of the environment. 861 01:00:57,190 --> 01:00:59,360 So you have maybe 10 different possibilities 862 01:00:59,360 --> 01:01:01,550 for the environment, and Fermi's golden rule 863 01:01:01,550 --> 01:01:03,610 gives you spontaneous emission, which 864 01:01:03,610 --> 01:01:05,810 is different for those 10 states. 865 01:01:05,810 --> 01:01:08,940 And naturally, since we have performed the partial trace 866 01:01:08,940 --> 01:01:12,000 over the environment, we have all those rates 867 01:01:12,000 --> 01:01:14,460 weighted with the probability that the environment 868 01:01:14,460 --> 01:01:16,850 is in one of those states. 869 01:01:16,850 --> 01:01:20,560 So what you find here is a simple generalization 870 01:01:20,560 --> 01:01:21,950 of Fermi's golden rule. 871 01:01:26,330 --> 01:01:36,980 And if you look at the off-diagonal matrix elements, 872 01:01:36,980 --> 01:01:39,260 for instance, you want to know what 873 01:01:39,260 --> 01:01:44,540 is this rate, what is the rate coefficient, which gives you 874 01:01:44,540 --> 01:01:48,130 the time derivative of the coherence, 875 01:01:48,130 --> 01:01:51,360 and it's multiplied with the coherence. 876 01:01:51,360 --> 01:01:56,640 You'll find now that in general, this rate coefficient has 877 01:01:56,640 --> 01:02:01,640 a damping term, but it may also have an imaginary term. 878 01:02:01,640 --> 01:02:05,320 And I hope you remember when we played with diagrams, that we 879 01:02:05,320 --> 01:02:07,040 had something similar. 880 01:02:07,040 --> 01:02:11,300 There was something which we called the radiative shift. 881 01:02:11,300 --> 01:02:14,800 I called it the AC stock effect of a single photon, 882 01:02:14,800 --> 01:02:17,170 and here it is a level shift which 883 01:02:17,170 --> 01:02:19,940 comes because the environment interacts with your system 884 01:02:19,940 --> 01:02:21,960 and it shifts the levels a little bit. 885 01:02:21,960 --> 01:02:23,940 So in addition to just relaxation, 886 01:02:23,940 --> 01:02:25,950 spontaneous emission, and damping, 887 01:02:25,950 --> 01:02:29,940 there is also a dispersive part, a level shift, 888 01:02:29,940 --> 01:02:35,950 and it has exactly the same structure. 889 01:02:35,950 --> 01:02:40,240 Let me add that delta ab is the difference 890 01:02:40,240 --> 01:02:46,470 between the shift of state b and the shift of state a. 891 01:02:46,470 --> 01:02:51,100 And those shifts have exactly the same structure. 892 01:02:51,100 --> 01:02:55,010 You have to take the principle part of something which 893 01:02:55,010 --> 01:02:58,070 has 1 over the difference of energies, 894 01:02:58,070 --> 01:03:02,390 and we discussed that this has to be understood 895 01:03:02,390 --> 01:03:07,930 by somewhere adding an infinitesimal imaginary part 896 01:03:07,930 --> 01:03:10,120 and doing the right thing with complex function. 897 01:03:10,120 --> 01:03:13,360 It's actually related to Laplace time difference 898 01:03:13,360 --> 01:03:17,590 between Laplace transformation and Fourier transformation. 899 01:03:17,590 --> 01:03:21,110 So anyway what I find sort of beautiful 900 01:03:21,110 --> 01:03:23,780 is that we started with a most general situation. 901 01:03:23,780 --> 01:03:25,400 We perform the partial trace. 902 01:03:25,400 --> 01:03:28,190 We made one assumption of short correlation times, 903 01:03:28,190 --> 01:03:31,880 and a lot of things we have known about quantum system 904 01:03:31,880 --> 01:03:34,310 just pops out in a very general form here. 905 01:03:37,060 --> 01:03:39,130 Any questions about so far? 906 01:03:49,280 --> 01:03:55,160 Well, the coherences are, of course, more interesting 907 01:03:55,160 --> 01:03:56,140 than the population. 908 01:03:56,140 --> 01:03:59,780 Coherence is always something physicists get excited about it 909 01:03:59,780 --> 01:04:03,000 because it captures something which goes often 910 01:04:03,000 --> 01:04:08,200 beyond classical system that we have 911 01:04:08,200 --> 01:04:10,170 quantum mechanical coherences. 912 01:04:10,170 --> 01:04:14,610 And what happens is the coefficient here, which 913 01:04:14,610 --> 01:04:18,700 provides the damping of the coherence, 914 01:04:18,700 --> 01:04:22,460 just comes out of the formalism, has two parts. 915 01:04:22,460 --> 01:04:34,040 And one part is an adiabatic part 916 01:04:34,040 --> 01:04:38,090 and the other one is a non-adiabatic part. 917 01:04:38,090 --> 01:04:39,940 Well, and that makes sense. 918 01:04:39,940 --> 01:04:42,710 If you have two quantum states and there 919 01:04:42,710 --> 01:04:45,886 is a coherence, some phase between the two, 920 01:04:45,886 --> 01:04:49,750 the phase can get lost if you do a transition between the two 921 01:04:49,750 --> 01:04:53,890 states or one state undergoes a collision and is quenched. 922 01:04:53,890 --> 01:04:58,480 So you definitely have one part which is due to the fact 923 01:04:58,480 --> 01:05:03,760 that the quantum states or the population 924 01:05:03,760 --> 01:05:08,660 changes, and you find that there is this state-changing part, 925 01:05:08,660 --> 01:05:11,760 which is pretty much the sum of all the rate 926 01:05:11,760 --> 01:05:14,030 coefficient leading out of state, 927 01:05:14,030 --> 01:05:16,310 leading to the decay of state a and leading 928 01:05:16,310 --> 01:05:18,810 to the decay of state b. 929 01:05:18,810 --> 01:05:21,560 In other words, if you have a two-level system, which 930 01:05:21,560 --> 01:05:29,510 has a coherence and you have decay of the excited 931 01:05:29,510 --> 01:05:31,640 state and decay of the ground state, 932 01:05:31,640 --> 01:05:36,430 you would expect that those decay terms appear also 933 01:05:36,430 --> 01:05:39,950 in the decay of the coherence between the two levels 934 01:05:39,950 --> 01:05:46,070 and they do, and they appear with the correct factor of 1/2. 935 01:05:46,070 --> 01:05:49,580 But there is another possibility and this is the following. 936 01:05:49,580 --> 01:05:54,540 You can have no [INAUDIBLE] of the population of the state, 937 01:05:54,540 --> 01:05:57,450 but you can still lose the coherence. 938 01:05:57,450 --> 01:05:59,360 The model you should maybe make is 939 01:05:59,360 --> 01:06:01,500 that you have spin up, spin down. 940 01:06:01,500 --> 01:06:03,920 You are not perturbing the populations 941 01:06:03,920 --> 01:06:06,650 in spin up and spin down, but the environment 942 01:06:06,650 --> 01:06:09,930 provides fluctuating magnetic field. 943 01:06:09,930 --> 01:06:13,680 Then due to the fluctuating magnetic field, 944 01:06:13,680 --> 01:06:16,240 you no longer can keep track of the phase, 945 01:06:16,240 --> 01:06:18,430 and that means in your identity matrix 946 01:06:18,430 --> 01:06:21,150 the off-diagonal matrix elements decay. 947 01:06:21,150 --> 01:06:25,670 And we find that here this is the second part which 948 01:06:25,670 --> 01:06:28,840 in this book is called the adiabatic part, 949 01:06:28,840 --> 01:06:32,090 and the physics behind it is now pure de-phasing. 950 01:06:35,210 --> 01:06:37,880 So it's an independent way for coherences 951 01:06:37,880 --> 01:06:42,275 to decay independent of the decay of the population. 952 01:06:56,374 --> 01:06:56,873 Questions? 953 01:06:59,900 --> 01:07:00,400 Collin. 954 01:07:00,400 --> 01:07:03,700 AUDIENCE: Where does the Markov approximation come in? 955 01:07:03,700 --> 01:07:06,730 PROFESSOR: The Markov approximation is, so to speak, 956 01:07:06,730 --> 01:07:10,040 the delta function approximation, 957 01:07:10,040 --> 01:07:14,740 which would say that-- I mean, I introduced the correlation 958 01:07:14,740 --> 01:07:16,710 function between the reservoir operator 959 01:07:16,710 --> 01:07:20,320 and said the correlation time tau c is very, very short. 960 01:07:20,320 --> 01:07:22,050 The Markov approximation would actually 961 01:07:22,050 --> 01:07:25,670 state that it would actually say in a more radical way 962 01:07:25,670 --> 01:07:29,360 the correlation time is 0. 963 01:07:29,360 --> 01:07:32,440 And the Bohr approximation, the fact 964 01:07:32,440 --> 01:07:35,940 that the reservoir is unchanged came 965 01:07:35,940 --> 01:07:39,190 in when we said the total density 966 01:07:39,190 --> 01:07:43,320 matrix for the second order expression just factorizes. 967 01:07:43,320 --> 01:07:45,690 It factorizes into the environment, 968 01:07:45,690 --> 01:07:48,850 which is just this density matrix of the environment. 969 01:07:48,850 --> 01:07:52,100 It's not changed by the interaction with the system. 970 01:07:52,100 --> 01:07:53,820 And this is the Bohr approximation. 971 01:07:53,820 --> 01:07:58,650 We just use the same expression for the reservoir independent 972 01:07:58,650 --> 01:08:00,610 of the measurements the reservoir has done. 973 01:08:04,340 --> 01:08:06,320 Other questions? 974 01:08:06,320 --> 01:08:06,834 Yes, Nancy. 975 01:08:06,834 --> 01:08:07,750 AUDIENCE: [INAUDIBLE]. 976 01:08:12,760 --> 01:08:15,020 PROFESSOR: This is something very general. 977 01:08:15,020 --> 01:08:16,990 Thank you actually for the question. 978 01:08:16,990 --> 01:08:30,140 Whenever we have some damping of the population, 979 01:08:30,140 --> 01:08:33,170 the coherence is only damped with a factor of 1/2. 980 01:08:37,740 --> 01:08:40,479 One way to explain it in a very simple way 981 01:08:40,479 --> 01:08:57,750 is, that if you have an amplitude alpha excited 982 01:08:57,750 --> 01:09:06,260 and alpha ground, the population in the excited state 983 01:09:06,260 --> 01:09:09,180 is this squared. 984 01:09:09,180 --> 01:09:13,470 So you sometimes make the model that the amplitude decays 985 01:09:13,470 --> 01:09:17,319 with gamma over 2, but the population 986 01:09:17,319 --> 01:09:22,290 is-- because you take the product, decays with gamma. 987 01:09:22,290 --> 01:09:27,580 So you would say alpha e and alpha g both decay 988 01:09:27,580 --> 01:09:30,200 with half the rate, but the probability 989 01:09:30,200 --> 01:09:33,689 is for the total rate, and the coherence 990 01:09:33,689 --> 01:09:37,109 is the product of the amplitudes. 991 01:09:37,109 --> 01:09:39,750 So therefore when you look at the coherence, 992 01:09:39,750 --> 01:09:42,680 this decays with 1/2 gamma e. 993 01:09:42,680 --> 01:09:46,350 This decays with 1/2 gamma g, and this is what you get here, 994 01:09:46,350 --> 01:09:51,120 1/2 gamma in state a, 1/2 gamma in state b. 995 01:09:51,120 --> 01:09:54,160 Whereas the probability to be in this state 996 01:09:54,160 --> 01:09:59,370 decays with twice that because the probability is squared. 997 01:09:59,370 --> 01:10:03,190 So you find that pretty much in any quantum mechanically 998 01:10:03,190 --> 01:10:05,420 corrects derivation, which you do 999 01:10:05,420 --> 01:10:07,515 about the decay of population coherences. 1000 01:10:26,654 --> 01:10:27,320 Other questions? 1001 01:10:32,230 --> 01:10:33,590 So we have done two things. 1002 01:10:33,590 --> 01:10:36,580 We have done the very, very simple derivation 1003 01:10:36,580 --> 01:10:39,440 using the beam splitter model where you may not even 1004 01:10:39,440 --> 01:10:42,680 notice where I did the Markov approximation because I jumped 1005 01:10:42,680 --> 01:10:44,320 from beam splitter to beam splitter 1006 01:10:44,320 --> 01:10:46,890 and left all the correlations behind. 1007 01:10:46,890 --> 01:10:49,940 Here in the most general calculation, 1008 01:10:49,940 --> 01:10:52,720 you have seen exactly where it enters, 1009 01:10:52,720 --> 01:10:56,140 but maybe now you have the full forest in front of you, 1010 01:10:56,140 --> 01:10:58,480 and you don't recognize the trees anymore. 1011 01:10:58,480 --> 01:11:02,910 So let me wrap up this lecture by now focusing 1012 01:11:02,910 --> 01:11:06,550 on the system we want to discuss further on, 1013 01:11:06,550 --> 01:11:13,930 namely a two-level system interacting with a vacuum 1014 01:11:13,930 --> 01:11:15,690 through spontaneous emission. 1015 01:11:15,690 --> 01:11:19,590 But I also want to make some generalizations. 1016 01:11:19,590 --> 01:11:27,040 I want to give you some generalizations about what 1017 01:11:27,040 --> 01:11:30,385 kind of environments are possible in quantum physics. 1018 01:11:34,150 --> 01:11:38,480 Let me just see how I do that. 1019 01:11:41,020 --> 01:11:45,960 So this part I actually owe to Professor [? Ikschuan ?] who 1020 01:11:45,960 --> 01:11:48,430 wonderfully compiled that. 1021 01:11:48,430 --> 01:11:50,740 So what I want to do now is, I want 1022 01:11:50,740 --> 01:11:53,640 to call your attention to the operator 1023 01:11:53,640 --> 01:11:56,550 form which, is rather unique. 1024 01:11:56,550 --> 01:12:01,680 Remember when we did second order perturbation theory, 1025 01:12:01,680 --> 01:12:08,350 we had sort of the commutator of v 1026 01:12:08,350 --> 01:12:11,020 with the commutator of v and rho. 1027 01:12:11,020 --> 01:12:15,670 This came from iterating the exact equation of motion 1028 01:12:15,670 --> 01:12:17,890 for the density matrix. 1029 01:12:17,890 --> 01:12:21,567 And you want to specialize that now to Jaynes-Cummings model. 1030 01:12:21,567 --> 01:12:23,400 I mean, in the end, at least in this course, 1031 01:12:23,400 --> 01:12:25,400 we always come back to the Jaynes-Cummings model 1032 01:12:25,400 --> 01:12:29,360 because it captures a lot of what we want to explore. 1033 01:12:29,360 --> 01:12:33,120 So the Jaynes-Cummings model in the rotating wave approximation 1034 01:12:33,120 --> 01:12:34,360 is very simple. 1035 01:12:34,360 --> 01:12:38,160 It raises the atom from ground to excited state 1036 01:12:38,160 --> 01:12:41,680 and destroys a photon, or it does the opposite. 1037 01:12:41,680 --> 01:12:45,280 So this is our simple interaction 1038 01:12:45,280 --> 01:12:48,390 between our system, the two-level atom 1039 01:12:48,390 --> 01:12:53,210 and our reservoir which is just the vacuum of all the modes. 1040 01:12:53,210 --> 01:12:56,680 And you, again, recognize what I said in general. 1041 01:12:56,680 --> 01:12:59,380 You usually always find it by linear form, 1042 01:12:59,380 --> 01:13:02,580 an operator which acts on the modes, 1043 01:13:02,580 --> 01:13:05,770 on the reservoir on the vacuum, and an operator which 1044 01:13:05,770 --> 01:13:06,628 acts on the vacuum. 1045 01:13:10,090 --> 01:13:13,990 Now, we want to make the explicit assumption 1046 01:13:13,990 --> 01:13:18,291 that the initial state of the reservoir is the vacuum state. 1047 01:13:18,291 --> 01:13:18,790 It's empty. 1048 01:13:21,800 --> 01:13:25,755 And I want to show you what is the structure 1049 01:13:25,755 --> 01:13:29,540 of the operators we obtain. 1050 01:13:29,540 --> 01:13:32,600 And so if you put v into here, you 1051 01:13:32,600 --> 01:13:37,100 have first the commutator with rho, which I write down here, 1052 01:13:37,100 --> 01:13:40,790 and then we have to take another commutator with v. 1053 01:13:40,790 --> 01:13:47,680 And the result of that is the following, 1054 01:13:47,680 --> 01:13:52,090 that when it comes to relaxation pauses, 1055 01:13:52,090 --> 01:13:55,940 based on the general structure of the time 1056 01:13:55,940 --> 01:14:01,450 evolution of quantum mechanics, we have this double commutator. 1057 01:14:01,450 --> 01:14:16,180 And the operator which, couples our system to the environment 1058 01:14:16,180 --> 01:14:18,740 is erasing and lower an operator. 1059 01:14:18,740 --> 01:14:21,560 I mean, the atom because it interacts with the environment 1060 01:14:21,560 --> 01:14:24,820 either absolves the photon or emits the photon. 1061 01:14:24,820 --> 01:14:29,420 But those operators, sigma plus and sigma minus, 1062 01:14:29,420 --> 01:14:34,100 appear now always as products because we 1063 01:14:34,100 --> 01:14:35,860 have two occurrences of the interaction, 1064 01:14:35,860 --> 01:14:41,410 v. But if you look at the double commutator structure, 1065 01:14:41,410 --> 01:14:44,790 the operator sigma plus sigma minus appears. 1066 01:14:44,790 --> 01:14:46,370 This is just the general structure 1067 01:14:46,370 --> 01:14:48,900 of this double commutator appears 1068 01:14:48,900 --> 01:14:51,930 to the left side of the atomic density matrix 1069 01:14:51,930 --> 01:14:54,390 to the right side of the atomic density matrix 1070 01:14:54,390 --> 01:14:57,430 and then there is the coarse term where the atomic density 1071 01:14:57,430 --> 01:14:59,210 matrix is in the middle of the two. 1072 01:15:09,230 --> 01:15:11,770 So this is actually something which 1073 01:15:11,770 --> 01:15:15,540 is very general and very important 1074 01:15:15,540 --> 01:15:19,550 in the theory of open quantum system. 1075 01:15:19,550 --> 01:15:26,050 What I'm discussing with you now is this famous Lindblad form. 1076 01:15:26,050 --> 01:15:30,030 And the story goes like that. 1077 01:15:30,030 --> 01:15:34,960 You want to know what are possible environments, not just 1078 01:15:34,960 --> 01:15:35,587 empty vacuum. 1079 01:15:35,587 --> 01:15:36,920 You can have fluctuating fields. 1080 01:15:36,920 --> 01:15:39,320 You can have, you name it. 1081 01:15:39,320 --> 01:15:44,470 But if you are saying that your environment interacts 1082 01:15:44,470 --> 01:15:47,330 with your system through an operator, 1083 01:15:47,330 --> 01:15:53,130 and our operator is now the operator sigma minus, which 1084 01:15:53,130 --> 01:15:58,800 is a spontaneous emission, you need heavy t. 1085 01:15:58,800 --> 01:16:02,740 The mathematical structure of a valid quantum field 1086 01:16:02,740 --> 01:16:06,490 remains that if your system interacts with an environment 1087 01:16:06,490 --> 01:16:09,280 by emitting a photon sigma minus, 1088 01:16:09,280 --> 01:16:14,050 this is now the structure of the master equation. 1089 01:16:14,050 --> 01:16:16,910 This is the structure of the time evolution of the density 1090 01:16:16,910 --> 01:16:17,730 matrix. 1091 01:16:17,730 --> 01:16:21,120 So the operator sigma minus and its 1092 01:16:21,120 --> 01:16:23,920 and its Hermitian conjugate sigma plus, all of this 1093 01:16:23,920 --> 01:16:28,330 have to appear in this combination. 1094 01:16:28,330 --> 01:16:28,830 Yes, Collin. 1095 01:16:28,830 --> 01:16:31,716 AUDIENCE: This is still in my interaction picture. 1096 01:16:31,716 --> 01:16:32,216 Right? 1097 01:16:32,216 --> 01:16:34,696 There's no dynamical phase evolution 1098 01:16:34,696 --> 01:16:38,144 that we put back in there. 1099 01:16:38,144 --> 01:16:38,810 PROFESSOR: Yeah. 1100 01:16:38,810 --> 01:16:39,570 OK. 1101 01:16:39,570 --> 01:16:43,460 What we do in general if the system is driven by a laser 1102 01:16:43,460 --> 01:16:46,230 beam, for instance, Rabi oscillation, 1103 01:16:46,230 --> 01:16:49,460 we simply add up the dynamics of the Rabi oscillation 1104 01:16:49,460 --> 01:16:54,294 of the unitary time evolution to the time evolution 1105 01:16:54,294 --> 01:16:55,210 done by the reservoir. 1106 01:16:55,210 --> 01:16:58,654 AUDIENCE: So this form is always in the interaction picture? 1107 01:16:58,654 --> 01:17:00,340 PROFESSOR: Well, this is, you would say, 1108 01:17:00,340 --> 01:17:04,540 this form is what is the relaxation provided 1109 01:17:04,540 --> 01:17:05,890 by the environment. 1110 01:17:05,890 --> 01:17:07,980 And if you drive the system in addition 1111 01:17:07,980 --> 01:17:11,450 with the coherent field, unitary time evolution, 1112 01:17:11,450 --> 01:17:15,250 you would add it to it. 1113 01:17:15,250 --> 01:17:17,970 So in other words, what I'm telling 1114 01:17:17,970 --> 01:17:21,340 you here is that this is the general structure, 1115 01:17:21,340 --> 01:17:23,400 and if you have a system which interacts 1116 01:17:23,400 --> 01:17:26,180 with an environment in five different ways, 1117 01:17:26,180 --> 01:17:29,090 with a dipole wand, with a magnetic moment and such, 1118 01:17:29,090 --> 01:17:32,320 you have maybe five interaction terms 1119 01:17:32,320 --> 01:17:35,920 and then you have to perform the sum over five operators, 1120 01:17:35,920 --> 01:17:39,150 and here one of them is a sigma minus operator. 1121 01:17:39,150 --> 01:17:42,410 So in other words, if you want to know 1122 01:17:42,410 --> 01:17:46,550 what is the whole world of possibilities for quantum 1123 01:17:46,550 --> 01:17:49,950 system to relax and dissipate with an environment, 1124 01:17:49,950 --> 01:17:52,610 you can pretty much take any operator which 1125 01:17:52,610 --> 01:17:55,990 acts on your system, but then put it 1126 01:17:55,990 --> 01:17:59,060 into this so-called Lindblad form 1127 01:17:59,060 --> 01:18:01,380 and you have a possible environment. 1128 01:18:04,560 --> 01:18:07,410 And I mentioned I think last week 1129 01:18:07,410 --> 01:18:11,060 that people are now in our field actively working 1130 01:18:11,060 --> 01:18:13,260 on environmental engineering. 1131 01:18:13,260 --> 01:18:16,870 They want to expose a system to an artificial environment 1132 01:18:16,870 --> 01:18:20,070 and hope the system is not relaxing, let's say, 1133 01:18:20,070 --> 01:18:23,690 to a broken ground state, but to a fancy correlated state. 1134 01:18:27,500 --> 01:18:32,160 So what this Lindblad form, if the operators appears 1135 01:18:32,160 --> 01:18:37,770 in this way, what it insures is the following. 1136 01:18:37,770 --> 01:18:40,800 Just imagine if we have an equation, 1137 01:18:40,800 --> 01:18:43,020 a derivative of the density matrix, 1138 01:18:43,020 --> 01:18:45,310 which depends on the density matrix, 1139 01:18:45,310 --> 01:18:48,080 you could write down a differential equation and say 1140 01:18:48,080 --> 01:18:49,430 is it possible? 1141 01:18:49,430 --> 01:18:52,240 Well, it has to be consistent with quantum physics. 1142 01:18:52,240 --> 01:18:53,980 You have certain requirements. 1143 01:18:53,980 --> 01:18:58,660 One requirement is that rho, the density matrix, 1144 01:18:58,660 --> 01:19:01,870 always has to be the density matrix. 1145 01:19:01,870 --> 01:19:04,270 The trace equal 1 has to be conserved. 1146 01:19:04,270 --> 01:19:09,190 A density matrix always must have non-negative eigenvalues, 1147 01:19:09,190 --> 01:19:10,740 otherwise, what you write down, it 1148 01:19:10,740 --> 01:19:13,200 might be a nice differential equation, but quantum 1149 01:19:13,200 --> 01:19:15,290 mechanically, it's nonsense. 1150 01:19:15,290 --> 01:19:20,940 But now there is one more thing, which is also necessary. 1151 01:19:20,940 --> 01:19:26,380 This time evolution of the system's density matrix 1152 01:19:26,380 --> 01:19:31,370 must come from a unitary time evolution of a bigger system. 1153 01:19:31,370 --> 01:19:35,190 So you must be able to extend your system into a bigger 1154 01:19:35,190 --> 01:19:36,890 system, which is now the environment, 1155 01:19:36,890 --> 01:19:40,710 and this whole system must follow a Schrodinger equation 1156 01:19:40,710 --> 01:19:43,760 with a Hamilton as a unitary time evolution. 1157 01:19:43,760 --> 01:19:46,030 And this is where it's restrictive. 1158 01:19:46,030 --> 01:19:49,050 You cannot just write down a differential equation and hope 1159 01:19:49,050 --> 01:19:51,140 that this will fill some requirement, 1160 01:19:51,140 --> 01:19:56,350 and what people have shown is under very general assumptions, 1161 01:19:56,350 --> 01:20:01,320 it is the Lindblad form which allows for it. 1162 01:20:01,320 --> 01:20:05,360 So some operator always has to appear in this form. 1163 01:20:08,120 --> 01:20:13,310 So often in this Lindblad form, you 1164 01:20:13,310 --> 01:20:18,070 have an operator, which is called a jump operator, which 1165 01:20:18,070 --> 01:20:20,390 is responsible for the measurement, which 1166 01:20:20,390 --> 01:20:22,610 the environment does on your system. 1167 01:20:22,610 --> 01:20:24,820 The jump operator is here, the operator 1168 01:20:24,820 --> 01:20:28,740 which takes the atom from the excited to the ground state. 1169 01:20:28,740 --> 01:20:32,480 With that you need a photon, and the photon can be measured. 1170 01:20:32,480 --> 01:20:37,910 So often you can describe a system by a jump operator, 1171 01:20:37,910 --> 01:20:41,130 and if the jump operator is put into this Lindblad form, 1172 01:20:41,130 --> 01:20:49,760 then you have a valid master equation for your system. 1173 01:20:52,270 --> 01:20:53,610 So let me wrap up. 1174 01:21:05,924 --> 01:21:10,320 If you take now the definition of the raising and lowering 1175 01:21:10,320 --> 01:21:14,540 operator, and you take the form I showed you, the Lindblad 1176 01:21:14,540 --> 01:21:21,052 form, you'll find now this differential equation 1177 01:21:21,052 --> 01:21:22,135 for your two-level system. 1178 01:21:24,900 --> 01:21:27,930 And this is one part of the Optical Bloch Equation. 1179 01:21:27,930 --> 01:21:30,420 Now, coming to Collin's question, 1180 01:21:30,420 --> 01:21:32,280 if you include the time evolution 1181 01:21:32,280 --> 01:21:35,600 of the classical field, this is a coherent evolution 1182 01:21:35,600 --> 01:21:37,610 of the Bloch vector, which I showed 1183 01:21:37,610 --> 01:21:39,790 at the beginning of the class, and we 1184 01:21:39,790 --> 01:21:44,620 add this and what I wrote down at the beginning of the class. 1185 01:21:44,620 --> 01:21:48,792 Then we find the famous Optical Bloch Equations 1186 01:21:48,792 --> 01:21:50,000 in the Jaynes-Cummings model. 1187 01:21:55,610 --> 01:22:00,730 So these are now the Optical Bloch Equations, 1188 01:22:00,730 --> 01:22:03,760 and I hope you enjoy now after this complicated discussion, 1189 01:22:03,760 --> 01:22:04,910 how simple they are. 1190 01:22:04,910 --> 01:22:07,700 And it is this simple set of equations, 1191 01:22:07,700 --> 01:22:10,650 which will be used in the rest of the course 1192 01:22:10,650 --> 01:22:13,480 to describe the time evolution of the system. 1193 01:22:20,430 --> 01:22:22,630 Just because I did some generalizations 1194 01:22:22,630 --> 01:22:26,020 about the Lindblad equation, I copied that into the lecture 1195 01:22:26,020 --> 01:22:29,230 notes from Wikipedia, and probably now you 1196 01:22:29,230 --> 01:22:33,680 sort of understand what is the most general Lindblad equation. 1197 01:22:33,680 --> 01:22:36,760 It has a Hamiltonian part and then it 1198 01:22:36,760 --> 01:22:41,070 has jump operators like you sigma minus operator, 1199 01:22:41,070 --> 01:22:45,100 but it has to come in the form that the jump 1200 01:22:45,100 --> 01:22:49,130 operator and its complex conjugate, emission. conjugate, 1201 01:22:49,130 --> 01:22:53,310 is on the left side, on the right side, and left and right 1202 01:22:53,310 --> 01:22:55,130 of your density matrix. 1203 01:22:55,130 --> 01:22:57,210 So this is the generalization I've mentioned. 1204 01:23:02,980 --> 01:23:05,720 Yeah. with that I think with that we've derived the master 1205 01:23:05,720 --> 01:23:09,250 equation, and on Wednesday, we will 1206 01:23:09,250 --> 01:23:13,270 look at rather simple solutions, transient and steady-state 1207 01:23:13,270 --> 01:23:16,830 solution of the Optical Bloch Equation. 1208 01:23:16,830 --> 01:23:20,110 Any questions? 1209 01:23:20,110 --> 01:23:22,410 One reminder about the schedule, this week 1210 01:23:22,410 --> 01:23:25,300 we have a lecture on Friday because I will not 1211 01:23:25,300 --> 01:23:28,120 be on town next week on Wednesday. 1212 01:23:28,120 --> 01:23:31,700 And of course, you know today in a week, next week on Monday. 1213 01:23:31,700 --> 01:23:32,890 It's [INAUDIBLE] day. 1214 01:23:32,890 --> 01:23:35,260 So we have three classes this week, 1215 01:23:35,260 --> 01:23:38,890 no class the following week, and then the normal schedule 1216 01:23:38,890 --> 01:23:41,040 for the rest of the semester.