Creation and Destruction Operators and Coherent States

Similar documents
PY 351 Modern Physics - Lecture notes, 3

Lecture 12. The harmonic oscillator

in terms of the classical frequency, ω = , puts the classical Hamiltonian in the form H = p2 2m + mω2 x 2

Simple Harmonic Oscillator

Quantum Physics III (8.06) Spring 2016 Assignment 3

1 Heisenberg Representation

Path integrals and the classical approximation 1 D. E. Soper 2 University of Oregon 14 November 2011

Second Quantization Method for Bosons

Many Body Quantum Mechanics

If electrons moved in simple orbits, p and x could be determined, but this violates the Heisenberg Uncertainty Principle.

Harmonic Oscillator. Robert B. Griffiths Version of 5 December Notation 1. 3 Position and Momentum Representations of Number Eigenstates 2

Massachusetts Institute of Technology Physics Department

( ) in the interaction picture arises only

Coherent states, beam splitters and photons

2 Quantization of the Electromagnetic Field

Quantum Mechanics Solutions. λ i λ j v j v j v i v i.

The Sommerfeld Polynomial Method: Harmonic Oscillator Example

Harmonic Oscillator with raising and lowering operators. We write the Schrödinger equation for the harmonic oscillator in one dimension as follows:

Quantum Physics III (8.06) Spring 2007 FINAL EXAMINATION Monday May 21, 9:00 am You have 3 hours.

Coherent states of the harmonic oscillator

Time dependent perturbation theory 1 D. E. Soper 2 University of Oregon 11 May 2012

Problems and Multiple Choice Questions

Lecture 6 Quantum Mechanical Systems and Measurements

Quantum Dynamics. March 10, 2017

2. As we shall see, we choose to write in terms of σ x because ( X ) 2 = σ 2 x.

1 The Quantum Anharmonic Oscillator

The Simple Harmonic Oscillator

SOLUTIONS for Homework #2. 1. The given wave function can be normalized to the total probability equal to 1, ψ(x) = Ne λ x.

Physics 741 Graduate Quantum Mechanics 1 Solutions to Midterm Exam, Fall x i x dx i x i x x i x dx

PHY 396 K. Problem set #5. Due October 9, 2008.

Comparison of Finite Differences and WKB Method for Approximating Tunneling Times of the One Dimensional Schrödinger Equation Student: Yael Elmatad

Physics 221A Fall 1996 Notes 16 Bloch s Theorem and Band Structure in One Dimension

Green Functions in Many Body Quantum Mechanics

5.1 Classical Harmonic Oscillator

Quantum Mechanics: Particles in Potentials

8.05 Quantum Physics II, Fall 2011 FINAL EXAM Thursday December 22, 9:00 am -12:00 You have 3 hours.

Chemistry 532 Problem Set 7 Spring 2012 Solutions

Chem 3502/4502 Physical Chemistry II (Quantum Mechanics) 3 Credits Spring Semester 2006 Christopher J. Cramer. Lecture 9, February 8, 2006

16. GAUGE THEORY AND THE CREATION OF PHOTONS

PHY4604 Introduction to Quantum Mechanics Fall 2004 Final Exam SOLUTIONS December 17, 2004, 7:30 a.m.- 9:30 a.m.

Atomic cross sections

Physics 606, Quantum Mechanics, Final Exam NAME ( ) ( ) + V ( x). ( ) and p( t) be the corresponding operators in ( ) and x( t) : ( ) / dt =...

Section 11: Review. µ1 x < 0

The Two Level Atom. E e. E g. { } + r. H A { e e # g g. cos"t{ e g + g e } " = q e r g

REVIEW: The Matching Method Algorithm

Lecture notes for QFT I (662)

The Hamiltonian and the Schrödinger equation Consider time evolution from t to t + ɛ. As before, we expand in powers of ɛ; we have. H(t) + O(ɛ 2 ).

arxiv:quant-ph/ v1 14 Mar 1999

5.74 Introductory Quantum Mechanics II

16.1. PROBLEM SET I 197

The Schrödinger Equation

PHYS 3313 Section 001 Lecture # 22

Problem Set # 8 Solutions

Physics 221A Fall 2018 Notes 8 Harmonic Oscillators and Coherent States

Second quantization: where quantization and particles come from?

B = 0. E = 1 c. E = 4πρ

Semiconductor Physics and Devices

Brief review of Quantum Mechanics (QM)

Damped harmonic motion

Page 404. Lecture 22: Simple Harmonic Oscillator: Energy Basis Date Given: 2008/11/19 Date Revised: 2008/11/19

Introduction to Quantum Mechanics (Prelude to Nuclear Shell Model) Heisenberg Uncertainty Principle In the microscopic world,

PHY 407 QUANTUM MECHANICS Fall 05 Problem set 1 Due Sep

1. For the case of the harmonic oscillator, the potential energy is quadratic and hence the total Hamiltonian looks like: d 2 H = h2

E = 1 c. where ρ is the charge density. The last equality means we can solve for φ in the usual way using Coulomb s Law:

Columbia University Department of Physics QUALIFYING EXAMINATION

Intent. a little geometry of eigenvectors, two-dimensional example. classical analog of QM, briefly

Basic Quantum Mechanics Prof. Ajoy Ghatak Department of Physics Indian Institute of Technology, Delhi

Lecture #9: Harmonic Oscillator: Creation and Annihilation Operators

C. Show your answer in part B agrees with your answer in part A in the limit that the constant c 0.

Dimensional analysis

Applied Nuclear Physics (Fall 2006) Lecture 2 (9/11/06) Schrödinger Wave Equation

Physics 221B Spring 2018 Notes 43 Introduction to Relativistic Quantum Mechanics and the Klein-Gordon Equation

ˆΨ( x) = 1 V. a k exp(i k x), (1) d 3 xd 3 x ˆΨ ( x) ˆΨ( x )V ( x x ) ˆΨ( x ) ˆΨ( x). (2) [a k, a k ] = δ k, k (3)

ON POSITIVE-OPERATOR-VALUED MEASURE FOR PHASE MEASUREMENTS. Abstract. The unnormalizable Susskind-Glogower (SG) phase eigenstates, which

1 Fundamental physical postulates. C/CS/Phys C191 Quantum Mechanics in a Nutshell I 10/04/07 Fall 2007 Lecture 12

t L(q, q)dt (11.1) ,..., S ) + S q 1

PHY4905: Intro to Solid State Physics. Tight-binding Model

E = hν light = hc λ = ( J s)( m/s) m = ev J = ev

Assignment 8. [η j, η k ] = J jk

Quantum mechanics in one hour

4.3 Lecture 18: Quantum Mechanics

Quantum Mechanics on Heisenberg group. Ovidiu Calin Der-Chen Chang Peter Greiner

arxiv: v7 [quant-ph] 22 Aug 2017

Lecture 14: Superposition & Time-Dependent Quantum States

Lecture 7. More dimensions

Physics 70007, Fall 2009 Answers to Final Exam

Optical Lattices. Chapter Polarization

Introduction to Path Integrals

Quantum Mechanics II

Opinions on quantum mechanics. CHAPTER 6 Quantum Mechanics II. 6.1: The Schrödinger Wave Equation. Normalization and Probability

Chemistry 3502/4502. Exam I Key. September 19, ) This is a multiple choice exam. Circle the correct answer.

Quantum Mechanics for Scientists and Engineers. David Miller

a = ( a σ )( b σ ) = a b + iσ ( a b) mω 2! x + i 1 2! x i 1 2m!ω p, a = mω 2m!ω p Physics 624, Quantum II -- Final Exam

Chemistry 3502/4502. Exam I. September 19, ) This is a multiple choice exam. Circle the correct answer.

Section 9 Variational Method. Page 492

Lecture #8: Quantum Mechanical Harmonic Oscillator

Qualifying Exam. Aug Part II. Please use blank paper for your work do not write on problems sheets!

Chemistry 432 Problem Set 4 Spring 2018 Solutions

Statistical Interpretation

Time evolution of states in quantum mechanics 1

Transcription:

Creation and Destruction Operators and Coherent States WKB Method for Ground State Wave Function state harmonic oscillator wave function, We first rewrite the ground < x 0 >= ( π h )1/4 exp( x2 a 2 h ) (1) In the notes on imaginary time path integrals, we obtained this formula from the imaginary time propagator for the harmonic oscillator. Before introducing creation and destruction operators, let us explore the exponential factor in the ground state wave functions. The method used is called the WKB (for Wentzel, Kramers, and Brillouin) method and involves a quantity closely related to the action used in the path integral discussion. We start by assuming the following form for a bound state wave function, Ψ = exp( W (x) ). (2) h Note that W has the same dimensions as h and the action S. Then we have and x Ψ = xw h Ψ, [ xψ 2 = ( xw h )2 2 xw h Let us use this formula in the Schrödinger equation, allowing an arbitrary potential for the moment. From ( ) h2 2m 2 x + V (x) Ψ = EΨ, we obtain ( ( xw ) 2 2m + V (x) + h 2 xw 2m ) ] Ψ Ψ = EΨ (3) Note that the first two terms on the left side are independent of h. The method we are using is semiclassical in which case it makes sense to try to solve the equation order by order in h. Now consider the eigenvalue E, in particular, suppose we are looking for the ground state of the system. For an oscillator the classical lowest energy is zero, and the actual ground state is hω/2. Let us follow this suggestion and assume for other potentials as well that for the ground state E O( h). Then if we make the terms independent of h cancel, we get ( x W ) 2 2m = V (x), or x W = 2mV (x)

which implies that W (x) = x x 0 dx 2mV (x ) The choice of x 0 is not completely specified. However, if we are looking for the ground state of the system, it makes sense to choose x 0 at the minimum of V (x). Returning to the oscillator, we obtain W (x) = x 0 dx 2mV (x ) = x 0 dx x = 1 2 x2, which when substituted in Eq.(2) gives the correct form of the oscillator ground state wave function. If we go further and match the O( h) terms in Eq.(3), assuming E is proportional to h, we get h 2 xw 2m = E. Using W (x) = x, this gives E = hω 2, which is the correct answer for the oscillator. This general method can be applied to other smooth potentials, but it is only exact for the oscillator. We will not pause to study the function W (x) further. The relation of W to the action S is basically that one trades the time t for the energy E, by making a so-called Legendre transform. More on this can be found in Classical Mechanics, by H. Goldstein. There is also much more to the WKB method than we have discussed here. It is more typical to use it for highly excited states of a particle moving in a smooth potential. In that case the particle can be in both the classically allowed region and the classically forbidden region. For the classically allowed region the form Ψ = exp(i W h ) is the appropriate one to use, and the factor of i in the exponent is replacedd by -1 when x moves into the classically forbidden region. For more on WKB and semiclassical quantum mechanics in general see Shankar, sec. 16.2, Gottfried and Yan, sec.2.8 and Chapter VII of Quantum Mechanics, by Landau and Lifshitz. Creation and Destruction Operators Now let us turn to the creation and destruction operators using our solutions of the Heisenberg equations of motion. Rewriting our previous results, X(t) = X cos ω 0 t + P sin ω 0 t, (4) 0 and P (t) = P cos ω 0 t + 0 X sin ω 0 t. (5)

By taking matrix elements of these equations between eigenstates, we found by matching time dependence on both sides, < n 1 X(t) n >= exp( iωt) < n 1 (X + i P ) n >, n 1 < n 1 (X i P ) n >= 0, all n, and < n + 1 X(t) n >= exp(iωt) < n + 1 (X i P ) n 0, < n 1 (X + i P ) n >= 0, all n, and further there is a set of states with energies hω(n + 1/2), n = 0, 1, 2,.... It is clear from these results that the operator (X + i P ) can only lead to n 1 > when acting on n >, while (X i P ) can only lead to n+1 > when acting on n >. Further since all states must have positive energy, we must have Let us multiply these operators. We have (X + i P ) 0 >= 0 (X i P )(X + i P ) = X2 + P 2 () 1 [P X XP ] 2 Multiplying by 2 /2 and using [P X XP ] = i h, we have Dividing by hω, we have 1 2 2 (X i P )(X + i P ) = H 1 2 hω H hω = 1 2 + 2 h (X i P )(X + i P ) The right hand side is dimensionless. We now define a 2 h (X + i P ),

and a 2 h (X i P ). The commutator of a with a follows from the X, P commutator. We have [a, a ] = 2 h [(X + i P ), (X i P )] = ī [P, X] = 1. h The harmonic oscillator Hamiltonian in terms of a and a is Rearranging Eqs.(4) and (5), we have X(t) = 1 2 H = hω(a a + 1 2 ) or using the definitions of a and a, we have Writing this equation one more time, so we have [(X i P ) exp(iωt) + (X + i P ) exp( iωt) ], h [ X(t) = a exp( iωt) + a exp(iωt) ] (6) 2 h [ X(t) = a(t) + a (t) ], 2 a(t) = a exp( iωt), a (t) = a exp(iωt), where a(t) and a (t) are the Heisenberg operators corresponding to the Schrödinger operators a and a. The corresponding expressions for P (t) follow from these, P (t) = m dx hω dt = i [ a exp( iωt) a exp(iωt) ] (7) 2m Expressions like Eqs.(6) and (7) occur in many more general problems, basically any problem that can be expanded in harmonic oscillators. Examples are photons, phonons, and the so-called vector mesons of particle physics, such as the W and Z particles. Let us now find the matrix elements of a and a. Using E n = hω(n + 1 2 ), we have < n (H hω ) n >= hωn. 2

But so we have H hω 1 2 = hω(a a), hωn = hω < n a a n > Now from our results above, we know that acting on n > a must lead exclusively to n 1 > so n 1 > is the only intermediate state that can be reached when we sandwich the identity between a and a. Cancelling the factor of hω, we have which gives n =< n a n 1 >< n 1 a n >= < n 1 a n > 2, n = < n 1 a n > 2. Choosing the possible phase factor to be 1, we have Rewriting these, we have which gives < n 1 a n >= n =< n a n 1 > a n >= n n 1 >, a n >= a a n >= n n > (n + 1) n + 1 >. so a a is a number (of excitations) operator. Let us show how to construct the states n > using a. Writing out the first few states, we have a 0 > = 1 > a 1 > = 2 2 > a 2 > = 3 3 >. a n > =. n + 1 n + 1 > Using these equations to express everything in terms of 0 >, we have n >= 1 (a ) n 0 > We can use this last equation to find the wave functions for all the states. Using a = 2 h (X i P ), we have < x n >= 1 ( 2 h )n/2 < x (X i P ) 0 >, or < x n >= 1 ( 2 h )n/2 (x h x) < x 0 >. This formula will generate the explicit form for < x n > for any n.

Coherent States Coherent states are an important class of states that can be realized by any system which can be represented in terms of a harmonic oscillator, or sums of harmonic oscillators. They are the answer to the question, what is the state of a quantum oscillator when it is behaving as classically as possible? As a practical example,the state of photons in a laser is quantum mechanical, but also behaves classically in many ways. Coherent states are relevant to this situation. The definition of a coherent state α > is that it is an eigenstate of a, the destruction operator, a α >= α α >, with < α α >= 1. From its definition, a is certainly not a self-adjoint operator, so it if has eigenstates at all, the eigenvalues need not be real, and in fact the value of α is any complex number. Minimum Uncertainty It is easy to show that coherent states exist, but let us first note one of their most characteristic properties, namely they have minimum Heisenberg uncertainty. Let us first express X and P in terms of a and a. We have X = x 0 (a + a ) P = ip 0 (a a ) where x 0 = p 0 = h 2 h 2 Now consider various expected values, < α X α >, < α X 2 α >, < α P α >, and < α P 2 α >. First note that < α a α > = α < α α > Finally, using < α α >= 1, we have < α a α > = (< α a α >) = α < α α >. < α X α > = x 0 (α + α ) < α P α > = ip 0 (α α ) In calculating < α X 2 α > and < α P 2 α >, the order of operators must treated with some care. We present the details for < α X 2 α >. We have < α X 2 α >= x 2 0 < α (a + a )(a + a ) α >= x 2 0 < α (aa + aa + a a + a a ) α > Most of these evaluate directly. For example, < α aa α >= α 2 < α α >, < α a a α >= α < α a α >= αα < α α >, and < α a a α >= (< α aa α >) = (α ) 2 < α α >. For

< α aa α >, we use the commutator [a, a ] = 1 and rewrite it as < α (a a + 1) α >= (αα + 1) < α α >. Finally, using < α α >= 1, we have < α XX α >= x 2 0(αα + 2αα + α α + 1) = x 2 0 From the results so far, we have Entirely similar steps give Putting these together, we have ( X) 2 =< α XX α > (< α X α >) 2 = x 2 0. ( P ) 2 =< α P α > (< α P α >) 2 = p 2 0. ( (α + α ) 2 + 1 ) ( X)( P ) = x 0 p 0 = h 2 which is the statement of minimum Heisenberg uncertainty. The steps just carried out have been done in the Schrödinger representation at t = 0. They go through equally well if we consider the uncertainties in X and P at an arbitrary time. This would be done by using Heisenberg opererators X(t) and P (t) in the above equations, which simply replace a by a exp( iωt) and a by a exp(iωt). The uncertainties in X(t) and P (t) remain x 0 and p 0, so minimum uncertainty continues to hold. Existence To demonstrate that coherent states exist, we first expand them in energy eigenstates of the harmonic oscillator, α >= n n >< n α >. Using a α >= α α > and a n >= n n 1 >, we have n + 1 n >< n + 1 α >. n α n >< n α >= n n 1 >< n α >= n Matching the coefficient of n > on both sides gives α < n α >= n + 1 < n + 1 α > Applying this equation for n = 0, 1, 2,... we have < 1 α > = α < 0 α > < 2 α > = α < 1 α > / 2 = α 2 < 0 α > / 2 < 3 α > = α < 2 α > / 3 = α 3 < 0 α > / 3 2. =. =.

The general result is then < n α >= αn < 0 α > Demanding normalization, we have or 1 =< α α >= n < n α > 2 = n 1 = exp( α 2 ) < 0 α > 2. ( α 2 ) n < 0 α > 2, Choosing a phase, we can set < 0 α >= exp( α 2 /2). We now have α >= exp( α 2 2 ) n α n n > This is a concrete formula for α >. Another, very convenient version is to make use of one of our previous formulas expressing n > in terms of repeated applications of a. This gives α >= exp( α 2 2 ) n α n (a ) n 0 >= exp( α 2 2 ) exp(αa ) 0 > Level of Excitation Given a coherent state, we may ask how the level of excitation and average energy are related to α. Define the number operator N = a a. When acting on an energy eigenstate, we have N n >= n n >. Taking the expected value of N in a coherent state, we obtain This allows us to express α as < N >=< α N α >=< α a a α >= α < α a α >= αα α =< N > exp(iϕ), where ϕ is a phase angle. Now for the expected value of the Hamiltonian, we have < H >=< α H α >= hω(< N > + 1 2 ) = hω(αα + 1 2 ) So given a certain average energy, the modulus of α is determined. To get insight into the meaning of the phase, consider the expected value of X(t) in a coherent state. We have < α X(t) α >= x 0 (α exp( iωt) + α exp(iωt) = x 0 α (exp( i(ωt ϕ)) + exp(i(ωt ϕ)), so < X(t) >= x 0 α 2 cos(ωt ϕ). From this we can see that if ϕ = 0, the oscillator expected value is that of a classical oscillator started at maximum displacement with

zero velocity, while if ϕ = π/2, the expected value is that of a classical operator started at zero displacement with maximum velocity. So far we see that in a coherent state, the value of α is in one-one correspondence with < N > or < H >. However, a coherent state is certainly not anywhere near an energy eigenstate. There is considerable spread around the n-value determined by < H >. To quantify this consider P n, the probability of a coherent state being found in the n-th eigenstate of the oscillator. We can write P n = < n α > 2 = ( α 2 ) n exp( α 2 ) Recalling that < N >= α 2, we may write P n as P n = < N >n exp( < N >), which is a Poisson distribution. A well-known property of a Poisson distribution is that ( N) 2 =< N 2 > < N > 2 is < N >. So there is considerable spread about < N >, but for large < N >, the average energy and level of excitation will appear to be well-defined. For example if < N >= 100, then N = 10. Thus an oscillator in a coherent state with a reasonably large α, will appear to have a well-defined energy to a classical observer. Nevertheless many states of excitation near the one defined by < N > are occupied.