A how to guide to second quantization method.

Similar documents
where the sums are over the partcle labels. In general H = p2 2m + V s(r ) V j = V nt (jr, r j j) (5) where V s s the sngle-partcle potental and V nt

PHYS 215C: Quantum Mechanics (Spring 2017) Problem Set 3 Solutions

Harmonic Oscillator, a, a, Fock Space, Identicle Particles, Bose/Fermi

763622S ADVANCED QUANTUM MECHANICS Solution Set 1 Spring c n a n. c n 2 = 1.

Advanced Quantum Mechanics

Inner Product. Euclidean Space. Orthonormal Basis. Orthogonal

PHYS 705: Classical Mechanics. Canonical Transformation II

Physics 181. Particle Systems

Density matrix. c α (t)φ α (q)

The Feynman path integral

ψ = i c i u i c i a i b i u i = i b 0 0 b 0 0

Homework Notes Week 7

12. The Hamilton-Jacobi Equation Michael Fowler

Lagrangian Field Theory

5.03, Inorganic Chemistry Prof. Daniel G. Nocera Lecture 2 May 11: Ligand Field Theory

10. Canonical Transformations Michael Fowler

THEOREMS OF QUANTUM MECHANICS

Quantum Mechanics for Scientists and Engineers. David Miller

Quantum Statistical Mechanics

Rate of Absorption and Stimulated Emission

5.62 Physical Chemistry II Spring 2008

1 (1 + ( )) = 1 8 ( ) = (c) Carrying out the Taylor expansion, in this case, the series truncates at second order:

Robert Eisberg Second edition CH 09 Multielectron atoms ground states and x-ray excitations

1 Vectors over the complex numbers

HW #6, due Oct Toy Dirac Model, Wick s theorem, LSZ reduction formula. Consider the following quantum mechanics Lagrangian,

From Biot-Savart Law to Divergence of B (1)

Foundations of Arithmetic

NOTES FOR QUANTUM GROUPS, CRYSTAL BASES AND REALIZATION OF ŝl(n)-modules

A particle in a state of uniform motion remain in that state of motion unless acted upon by external force.

APPENDIX A Some Linear Algebra

This model contains two bonds per unit cell (one along the x-direction and the other along y). So we can rewrite the Hamiltonian as:

C/CS/Phy191 Problem Set 3 Solutions Out: Oct 1, 2008., where ( 00. ), so the overall state of the system is ) ( ( ( ( 00 ± 11 ), Φ ± = 1

Lectures - Week 4 Matrix norms, Conditioning, Vector Spaces, Linear Independence, Spanning sets and Basis, Null space and Range of a Matrix

Canonical transformations

Workshop: Approximating energies and wave functions Quantum aspects of physical chemistry

ON MECHANICS WITH VARIABLE NONCOMMUTATIVITY

Section 8.3 Polar Form of Complex Numbers

COMPLEX NUMBERS AND QUADRATIC EQUATIONS

Dynamics of a Superconducting Qubit Coupled to an LC Resonator

One can coose te bass n te 'bg' space V n te form of symmetrzed products of sngle partcle wavefunctons ' p(x) drawn from an ortonormal complete set of

Solutions to Problems Fundamentals of Condensed Matter Physics

ELASTIC WAVE PROPAGATION IN A CONTINUOUS MEDIUM

Implicit Integration Henyey Method

PHYS 705: Classical Mechanics. Newtonian Mechanics

Non-interacting Spin-1/2 Particles in Non-commuting External Magnetic Fields

Salmon: Lectures on partial differential equations. Consider the general linear, second-order PDE in the form. ,x 2

The Order Relation and Trace Inequalities for. Hermitian Operators

ψ ij has the eigenvalue

Phys304 Quantum Physics II (2005) Quantum Mechanics Summary. 2. This kind of behaviour can be described in the mathematical language of vectors:

Ph 219a/CS 219a. Exercises Due: Wednesday 23 October 2013

Multi-electron atoms (11) 2010 update Extend the H-atom picture to more than 1 electron: H-atom sol'n use for N-elect., assume product wavefct.

8.323 Relativistic Quantum Field Theory I

PHYS 705: Classical Mechanics. Calculus of Variations II

Lecture notes for FYS KJM 4480

THE SUMMATION NOTATION Ʃ

EPR Paradox and the Physical Meaning of an Experiment in Quantum Mechanics. Vesselin C. Noninski

PHY688, Statistical Mechanics

Lecture 6/7 (February 10/12, 2014) DIRAC EQUATION. The non-relativistic Schrödinger equation was obtained by noting that the Hamiltonian 2

Lecture 3: Probability Distributions

Difference Equations

Lecture 14: Forces and Stresses

Econ107 Applied Econometrics Topic 3: Classical Model (Studenmund, Chapter 4)

Mathematical Preparations

The non-negativity of probabilities and the collapse of state

Einstein-Podolsky-Rosen Paradox

CHAPTER 14 GENERAL PERTURBATION THEORY

Lecture 20: Noether s Theorem

8. Superfluid to Mott-insulator transition

The Dirac Equation for a One-electron atom. In this section we will derive the Dirac equation for a one-electron atom.

Open string operator quantization

Representation theory and quantum mechanics tutorial Representation theory and quantum conservation laws

Structure and Drive Paul A. Jensen Copyright July 20, 2003

arxiv:quant-ph/ Jul 2002

Scattering of two identical particles in the center-of. of-mass frame. (b)

Errors for Linear Systems

2.3 Nilpotent endomorphisms

Linear Regression Analysis: Terminology and Notation

Quantum Mechanics I Problem set No.1

Introduction to Vapor/Liquid Equilibrium, part 2. Raoult s Law:

Chapter Twelve. Integration. We now turn our attention to the idea of an integral in dimensions higher than one. Consider a real-valued function f : D

Chapter Newton s Method

LECTURE 9 CANONICAL CORRELATION ANALYSIS

Linear Approximation with Regularization and Moving Least Squares

Open Systems: Chemical Potential and Partial Molar Quantities Chemical Potential

Week 2. This week, we covered operations on sets and cardinality.

Full Configuration Interaction Monte Carlo Studies of Quantum Dots

1 Derivation of Rate Equations from Single-Cell Conductance (Hodgkin-Huxley-like) Equations

CHAPTER 6. LAGRANGE S EQUATIONS (Analytical Mechanics)

Module 9. Lecture 6. Duality in Assignment Problems

Lecture 12: Discrete Laplacian

j) = 1 (note sigma notation) ii. Continuous random variable (e.g. Normal distribution) 1. density function: f ( x) 0 and f ( x) dx = 1

Limited Dependent Variables

THE VIBRATIONS OF MOLECULES II THE CARBON DIOXIDE MOLECULE Student Instructions

8.4 COMPLEX VECTOR SPACES AND INNER PRODUCTS

Physics 5153 Classical Mechanics. Principle of Virtual Work-1

5.04, Principles of Inorganic Chemistry II MIT Department of Chemistry Lecture 32: Vibrational Spectroscopy and the IR

SL n (F ) Equals its Own Derived Group

Affine and Riemannian Connections

8.323: QFT1 Lecture Notes

CHAPTER 5: Lie Differentiation and Angular Momentum

Transcription:

Phys. 67 (Graduate Quantum Mechancs Sprng 2009 Prof. Pu K. Lam. Verson 3 (4/3/2009 A how to gude to second quantzaton method. -> Second quantzaton s a mathematcal notaton desgned to handle dentcal partcle systems (Boson or Fermons. It also allows one to deal wth systems wth varables number of partcles (e.g. creaton and annhlaton of photon, creaton of electron-postron par. We wll explan later why ths method s called second quantzaton. -> A generc N-dentcal partcle Hamltonan (non-relatvstc: H ˆ = N = h ˆ ( p r, r + 2 N = j V ˆ nt ( r r j (, where h ˆ ( p r, r = p2 2m + V (r r s the sngle-partcle hamltonan and V ˆ nt s the nteracton between partcles (typcally par-wse nteracton. -> Bass set: Let { φ n >} be a complete set of sngle-partcle states where n s a collectve quantum ndex whch ncludes the spn ndex. A convenent set s the egenstates of h ˆ,.e. h ˆ φ n >= ε n φ n >. Any many-body state Ψ > can be expressed as a lnear combnaton of the drect product state of φ's subjected to the restrcton mposed by symmetrzaton (Bosons or ant-symmetrzaton (Fermons. Example: A two-electron state of He-atom where one electron s n S > and one electron s n 2S > s wrtten as Ψ S,2S >= A { S > 2S > } = S > 2S > 2S > S > 2 { } (2 where A s the ant-symmetrzaton operator and we wrote out the ant-symmetrzed state explctly, In ths notaton, t s understood that the frst ket s for electron and the second ket s for electron 2,.e., the wavefuncton corresponds to ths state s gven by Ψ S,2S (,2 < 2 < = { 2 φ (φ (2 φ (φ (2 S 2S 2S S } S > 2S > 2S > S > 2 { } (3 Note: Ths wavefuncton s ant-symmetrc wth respect to nterchange of partcle labels ( & 2, or nterchange of the state labels (S & 2S.

Ths notaton s perfectly fne but t s knd of slly because whch s electron and whch s electron 2 ; they are dentcal! In fact, the many-body state s unquely specfed by the statng whch sngle-partcle state s occuped, one electron s n S > and one electron s n 2S > and whether the partcles are Fermons or Bosons. Ths realzaton leads to a new notaton (second quantzaton. -> Second Quantzaton Notaton Instead of lnng up product state as st partcle, 2nd partcle, etc, one can lne up the sngle-partcle bass states. For example, st poston s S >, 2nd poston s S >, 3rd poston s 2S >, 4th poston s 2S >, etc., up to nfnte postons. The state Ψ S,2S > s denoted by Ψ S,2S >=,0,0,,0,... > (4 where and 0 are the occupaton number of the correspondng sngle-partcle bass state (we wll deal wth symmetrzaton and ant-symmetrzaton later. A general many-body state s denoted by Ψ >= n,n 2,...,n,...> n = 0or n can be 0,,2,3,.. forfermons for Bosons (5 The number of partcles representaton by ths state s N = n, (6 hence ths notaton allows one to represented a state wth varable number of partcles,.e. a lnear combnaton of states whose partcle numbers are dfferent. The Hlbert space spanned by ths set of bass states { n,n 2,...,n,...>} s called the occupaton number space or the Fock space. -> Creaton and annhlaton operators Borrowng the concepts of rasng and lower operators of harmonc oscllator, one can defne the vacuum state, the creaton operator and the annhlaton operator. The vacuum state s defned as a state wth zero partcle: Ψ vac > 0,0,0,...> 0 > (7 where 0> s the shorthand notaton. A state wth one partcle n the th sngle-partcle state can be denoted by the creaton operator, a +, actng on the vacuum state: 0,...,,... >= a + 0 >. 2

One can thnk of the creaton operator creates one partcle (or rasng the occupaton number by one. You may ask, what exactly s ths creaton operator and how does t rase the occupaton number by one?. Remember, we are merely defnton notaton rght now, let s determne what propertes these creaton operators must obey. For example, f the partcles are Fermons, then creaton one more partcle n the th state s not allowed hence a + a + 0 >= 0 (Fermons. (8 Note: The rght-hand sde s the number zero, not the vacuum state, whch s denoted by a ket. One the other hand, f the partcles are Bosons, then a + a + 0 >= a + 0,...,...>= 2 0,...2,... > 0,...2,...>= 2 a + a + 0 > (Bosons (9 The 2 s needed for normalzaton. In general, a + 0,...n,... >= n + 0,...n +,... > (a + n 0 >= n! 0,...n,...> 0,...n,...>= n! (a + n 0 > (0 These formulae are vald for both Bosons and Fermons, one must remember that for Fermons, n can only be 0 or. Lkewse the annhlaton operators have these propertes: a 0,...n,... >= n 0,...n,...> In partcular, a 0 >= 0 = 0 Agan, these formulae are vald for both Bosons and Fermons, one must remember that for Fermons, n can only be 0 or. ( One can easly show that a + a 0,...n,...>= n 0,...n,...> <,...n,...0 a + a 0,...n,...>= n (2 Hence a + a s the (occupaton number operators. You see that these propertes are those of the harmonc oscllators. There are other propertes such as symmetry/ant-symmetry under partcle label exchange (or equvalently state label exchange A state wth one partcles n the th state and one partcles n the jth state s denoted by 3

a j + a + 0 >= 0,...,n =,...,n j =,..0,. > (3 Now how do we embedded n ths notaton that Bosonc state s symmetrc and Fermonc states are ant-symmetrc? ** We wll use the conventon that f <j, that s the th state s order before j n then we choose a postve sgn, as ndcated n Eq.(3 The exchange property s denoted by a + a j + 0 >= a j + a + 0 > (Bosons a + a j + 0 >= a j + a + 0 > (Fermons (4 The amazng thng s that all the above propertes can be easly and automatcally takng care of f we mpose the followng commutaton rules for Bosons and ant-commutaton rules for Fermons (for more rgorously dervaton, see Fetter and Walecka. [a,a j + ] = δ j, [a,a j ] = 0, [a +,a j + ] = 0 (Bosons + { a,a j } = δ j, { a,a j } = 0, a + + {,a j } = 0 (Fermons Cummutaton [A,B] AB- BA Ant- cummutaton { A,B} AB + BA (5 -> Feld Operators One thng about these notatons s that one has to remnd the readers what are the chosen sngle partcle bass states. There s a way to do ths by defnng the so-called feld operator, ( r + ( r φ ( r a φ *( r + a (We have put the ˆ over the ψ's to remnd you that they are operators + ( r ( r d 3 r = a + a = ˆ (We have appled the orthogonalty propertes of the bass states n where φ n ( r s the sngle partcle bass functon, agan n s a collectve quantum ndex ncludng the spn state. The nterpretaton of + ( r ( r d 3 r s an operator whch wll gve you the total number of partcle n the system, hence + ( r ( r s the partcle densty operator. These are operators, you wll get a number only after you compute the expectaton of these operators wth 4 (6

the state whch s expressed n the occupaton number space (Fock space. Often, t s convenent to defne the feld operator for a partcular sngle partcle spn state, ( r ( r φ, ( r a, φ, *( r + a, ( r ( r d 3 r = a + a, = ˆ, n, (Example: For spn / 2 partcles, could be or (7 The feld operator defned n Eq (6 s related to these operators by ( r = ( r Now, ( r ( r s the partcle densty for the spn state. The commutaton/ant commutaton relatons for the feld operators can be derved from the correspondng commutaton/ant commutaton relatons for the a and a+ (plus the completeness property of the sngle partcle bass functons Bosons: ( r, + ( r ' β ( r, β ( r ' ( r, + β ( r ' [ ] = δ β δ( r [ ] = 0 [ ] = 0 Fermons: ( r, + β ( r ' ( r, β ( r ' ( r, + β ( r ' { } = δ β δ( r { } = 0 { } = 0 r r ' r r ' (8 -> Why s t called second quantzaton? Frst quantzaton refers to the quantzaton procedure whch changes the classcal Posson brackets of dynamcal varables to the quantum commutaton relaton, for example 5

[ f,g]posson f g bracket p x f g x p Example: [ p, x]posson = bracket [ p, x] Quantum = h Frst Quantzaton Rule: [ f,g] Quantum = h[ f,g]posson bracket (9 Second quantzaton refers to the commutaton/ant-commutaton rules mposed on the a and a+ as stated n Eq. (5 or on the feld operators as stated n Eq. (8. -> Expressng the many-body hamltonan n second quantzed notaton. To change the Hamltonan from frst operators to second quantzaton operators, one computes the matrx element of H (from Eq. between bass states n the followng manner ˆ H 2nd quantzaton = ( r h ˆ β ( r d 3 r + 2,β,β,',β ' ˆ + ( r ' ( r V nt ( r, r ' β ( r ( β ' ( r 'd 3 r ψ ' ˆ H 2nd quantzaton 2,β,',β ' = a +, < φ, h ˆ φ > a + j,β j,β ',, j, j',β, j a +,'' a +, < φ ',' ( r 'φ, ( r V nt ( r, r ' φ j,β ( r φ j',β ' ( r ' > a j,β a j,β ' Typcally the frst quantzed hamltonan has no spn dependence, then β = ˆ H 2nd quantzaton 2,' ',, j, j' = a +, < φ, h ˆ φ j, > a j, +, j a + ',' a +, < φ ',' ( r 'φ, ( r V nt ( r, r ' φ j, ( r φ j',' ( r ' > a j, a j',' (20 If we assume the sngle - partcle bass states are the egenstates of ˆ h, then ˆ H 2nd quantzaton 2,' ',, j, j' = a +, ε a, + a + ',' a +, < φ ',' ( r 'φ, ( r V nt ( r, r ' φ j, ( r φ j',' ( r ' > a j, a j',' 6

-> Fnd the egenstate of H In general t s not possble to fnd the exact energy egenstate of a many-body Hamltonan. One often guess a tral state, for example of a Fermon system, a tral ground state could be a sngle Slater determnat maded up of the lowest sngle partcle states subjected to the Paul-exlcuson prncple. For example, Be atom has four electrons; one may guess the grond state be (S (S (2S (2S, or n second quantzaton notaton: + Ψ >= a + 2S a + + S 0 > (2 The approxmate ground state energy s gven by E o tral =< Ψ ˆ H 2nd quantzed Ψ >=< 0 a S H ˆ 2nd a + S 0 > (22 quantzed The terms n H whch contrbute are the a s and a+ s whch match the labels n the state. For example, the sngle partcle term < 0 a S a,, + ε =< 0 a S a,, + ε a, + a + 2S a + + S 0 > a + 2S a + 2S a + S a + S a, 0 >= 0 f, S,S,2S,2S that s, f a j, s NOT any one of a + 2S a + 2S a + S a + S, then we can move a j, to the rght (generate a negatve sgn for every nterchange and act on the vacuum whch gves zero. In fact, a +, a, = n ˆ, s the number operator and a sngle Slater determnat ( Ψ > s an egenstate of the number operator,, a +, a, Ψ >= n ˆ, Ψ >= n, Ψ > (the last n, s a number = n ˆ, (23 Hernce, < 0 a S a,, j + ε a j, + a + 2S a + + S 0 >= 2ε S + 2ε 2S. For the par-wse nteracton, here are some of the non-zero contrbutons: 7

S a S <S ' S V nt S S ' > a S (The subscrpt,' s to remnd you that snce V nt has no spn - dependence, the orthogonalty of the spn states the nner states and the outer states must have the same spn state respectvely. Now we remove the subscrbe for smply the notaton. We wth move the to the left two space (every nchange gve one negatve sgn so that we can group the operators nto number operators, lke ths: = 2 <SS V nt SS > (a + S (a + S a S Smlarly for other terms: S <SS V nt SS > a S = 2 <SS V nt SS > (a + S a S (a + S 2S < 2S2S V nt 2S2S > = 2 < 2S2S V nt 2S2S > (a + 2S (a + 2S 2S < 2S2S V nt 2S2S > = 2 < 2S2S V nt 2S2S > (a + 2S (a + 2S For states wth the same spn (t has a drect term and an exchange term S 2S 2S S < 2SS V nt 2SS > = 2 < 2SS V nt 2SS > (a + S ( <S2S V nt 2SS > = 2 <S2S V nt 2SS > (a + S (a + 2S <S2S V nt 2SS > = 2 <S2S V nt 2SS > (a + 2S (a + S < 2SS V nt 2SS > = 2 < 2SS V nt 2SS > (a + 2S (a + S (Why don't we get an exchange term for unlke spns? + 8