Time-Dependent Perturbation Theory

Slides:



Advertisements
Similar presentations
Non-degenerate Perturbation Theory
Advertisements

Quantum One: Lecture 3. Implications of Schrödinger's Wave Mechanics for Conservative Systems.
Review Three Pictures of Quantum Mechanics Simple Case: Hamiltonian is independent of time 1. Schrödinger Picture: Operators are independent of time; state.
PH 401 Dr. Cecilia Vogel. Review Outline  Time dependent perturbations  approximations  perturbation symmetry  Sx, Sy, Sz eigenstates  spinors, matrix.
Chapter 3 Formalism. Hilbert Space Two kinds of mathematical constructs - wavefunctions (representing the system) - operators (representing observables)
4. The Postulates of Quantum Mechanics 4A. Revisiting Representations
Density Matrix Density Operator State of a system at time t:
Physics 3 for Electrical Engineering
Nanostructures Research Group CENTER FOR SOLID STATE ELECTRONICS RESEARCH Time-Dependent Perturbation Theory David K. Ferry and Dragica Vasileska Arizona.
Chap 3. Formalism Hilbert Space Observables
Quantum Two 1. 2 Time Independent Approximation Methods 3.
Operators A function is something that turns numbers into numbers An operator is something that turns functions into functions Example: The derivative.
Ch ; Lecture 26 – Quantum description of absorption.
1 Three views on Landau damping A. Burov AD Talk, July 27, 2010.
Lecture 26 Molecular orbital theory II
Quantum Mechanical Cross Sections In a practical scattering experiment the observables we have on hand are momenta, spins, masses, etc.. We do not directly.
Introduction to Time dependent Time-independent methods: Kap. 7-lect2 Methods to obtain an approximate eigen energy, E and wave function: perturbation.

Mathematical Tools of Quantum Mechanics
Quantum Two 1. 2 Time Independent Approximation Methods 3.
Physics 452 Quantum mechanics II Winter 2011 Karine Chesnel.
Time Dependent Perturbation Theory
Chapter 4 Two-Level Systems, Spin. Two-level systems Let us start with the simplest non-trivial state space, with only two dimensions Despite its simplicity,
Quantum Two 1. 2 Time-Dependent Perturbations 3.
Introduction to Coherence Spectroscopy Lecture 1 Coherence: “A term that's applied to electromagnetic waves. When they "wiggle" up and down together they.
Chapter 9 Spin. Total angular momentum Let us recall key results for the total angular momentum 6.B.2 6.C.1.
MODULE 13 Time-independent Perturbation Theory Let us suppose that we have a system of interest for which the Schrödinger equation is We know that we can.
Chapter 3 Postulates of Quantum Mechanics. Questions QM answers 1) How is the state of a system described mathematically? (In CM – via generalized coordinates.
QM2 Concept Test 14.3 Choose all of the following statements that are correct when incoherent thermal radiation acts as a perturbation on the hydrogen.
Systems of Identical Particles
Chapter 4 Dynamical Behavior of Processes Homework 6 Construct an s-Function model of the interacting tank-in-series system and compare its simulation.
Quantum optics Eyal Freiberg.
Chapter 4 Dynamical Behavior of Processes Homework 6 Construct an s-Function model of the interacting tank-in-series system and compare its simulation.
Density Matrix Density Operator State of a system at time t:
Time Dependent Perturbation Theory
Open quantum systems.
Concept test 15.1 Suppose at time
Chapter 6 Angular Momentum.
Non-degenerate Perturbation Theory
Chapter 3 Formalism.
Perturbation Theory Lecture 2 Books Recommended:
Stationary Perturbation Theory And Its Applications
Quantum One.
Spin and Magnetic Moments
4. The Postulates of Quantum Mechanics 4A. Revisiting Representations
The Harmonic Oscillator
Concept test 15.1 Suppose at time
Chapter 9 Spin.
Victor Edneral Moscow State University Russia
12. Approx. Methods for Time Ind. Systems
Quantum mechanics II Winter 2012
Quantum One.
Chapter 4 Two-Level Systems.
Perturbation Theory Lecture 4.
Quantum Two Body Problem, Hydrogen Atom
Note: For the following concept tests about time-dependent perturbation theory, The general state of a two-state system system at time
Quantum mechanics II Winter 2012
Joseph Fourier ( ).
Approximation Employed in Spontaneous Emission Theory / D. F
Addition of Angular Momenta
Hour 33 Coupled Oscillators I
Chapter 5 1D Harmonic Oscillator.
LECTURE 15.
Perturbation Theory Lecture 3.
Particle oscillations in COLLAPSE models
QM2 Concept Test 11.1 In a 3D Hilbert space,
Linear Vector Space and Matrix Mechanics
QM2 Concept Test 10.1 Consider the Hamiltonian
Lecture 15: Time-Dependent Perturbation
Presentation transcript:

Time-Dependent Perturbation Theory Chapter 13 Time-Dependent Perturbation Theory

13.A The eigenproblem Let us assume that we have a system with an (unperturbed) Hamiltonian H0, the eigenvalue problem for which is solved and the spectrum is discrete and non-degenerate: The eigenstates form a complete orthonormal basis: At t = 0, a small perturbation of the system is introduced so that the new Hamiltonian is: At t < 0, the system is in the stationary state

13.A The eigenproblem At t > 0, the system evolves and can be found in a different state What is the probability of finding the system at time t in another eigenstate of the unperturbed Hamiltonian ? The evolution of the system is described by the Schrödinger equation: Then:

The approximate solution 13.B.1 The approximate solution Let us employ the following expansion: Where: Then:

The approximate solution 13.B.1 The approximate solution Let us employ the following expansion: Where: Then:

The approximate solution 13.B.1 The approximate solution Let us employ the following expansion: Where: Then:

The approximate solution 13.B.1 The approximate solution

The approximate solution 13.B.1 The approximate solution

The approximate solution 13.B.1 The approximate solution If the perturbation is zero: With a non-zero perturbation we can look for the solution in the form: Then:

The approximate solution 13.B.1 The approximate solution If the perturbation is zero: With a non-zero perturbation we can look for the solution in the form: Then:

The approximate solution 13.B.2 The approximate solution This equation is equivalent to the Schrödinger equation We will look for the solutions in the following form:

The approximate solution 13.B.2 The approximate solution This equation is equivalent to the Schrödinger equation We will look for the solutions in the following form:

The approximate solution 13.B.2 The approximate solution For the 0th order: For the higher orders: From the 0th order solution we can recursively restore solutions for the higher orders

13.B.3 First order solution Let us recall that at t < 0, the system is in the stationary state Therefore: And: Since: Then:

13.B.3 First order solution Let us recall that at t < 0, the system is in the stationary state Therefore: And: Since: Then:

First order solution So, for this equation: The solution is: 13.B.3 First order solution So, for this equation: The solution is: Let us recall the formula for the probability:

First order solution So, for this equation: The solution is: 13.B.3 First order solution So, for this equation: The solution is: Let us recall the formula for the probability:

First order solution So, for this equation: The solution is: 13.B.3 First order solution So, for this equation: The solution is: Let us recall the formula for the probability: So, if i ≠ f, then:

13.B.3 First order solution Thereby, to the lowest power of λ, the probability we are looking for is: It is nothing else but the square of the modulus of the Fourier transformation of the perturbation matrix element (coupling)

Example: sinusoidal perturbation 13.C.1 Example: sinusoidal perturbation Let’s assume that the perturbation is: In this case: Where: Now we can calculate:

Example: sinusoidal perturbation 13.C.1 Example: sinusoidal perturbation Let’s assume that the perturbation is: In this case: Where: Now we can calculate:

Example: sinusoidal perturbation 13.C.1 Example: sinusoidal perturbation Let’s assume that the perturbation is: In this case: Where: Now we can calculate:

Example: sinusoidal perturbation 13.C.1 Example: sinusoidal perturbation So, if the perturbation is: The probability is: On the other hand, if the perturbation is: Then the probability is:

Example: sinusoidal perturbation 13.C.1 13.C.2 Example: sinusoidal perturbation On the other hand, if the perturbation is: Then the probability is:

Example: sinusoidal perturbation 13.C.2 Example: sinusoidal perturbation The probability of transition is greatest when the driving frequency is close to the “natural” frequency: resonance The width of the resonance line is nothing else by the time-energy uncertainty relation On the other hand, if the perturbation is: Then the probability is:

Example: sinusoidal perturbation 13.C.2 Example: sinusoidal perturbation As a function of time, the probability oscillates sinusoidally To increase the chances of transition to occur, the perturbation does not necessarily have to be kept on for a long time On the other hand, if the perturbation is: Then the probability is:

Example: sinusoidal perturbation 13.C.1 Example: sinusoidal perturbation For the special case: The probability is: On the other hand, if the perturbation is: Then the probability is:

Example: sinusoidal perturbation 13.C.1 Example: sinusoidal perturbation For the special case: The probability is:

Coupling with the states of the continuous spectrum So far we assumed that the final state belongs to a discrete part of the spectrum How is the theory modified if the energy Ef belongs to a continuous part of the spectrum of H0? First of all, we cannot measure a probability of finding the system in a well-defined final state Instead, one has to employ integration over a certain group of final states

Coupling with the states of the continuous spectrum Let us assume that we have a system with an (unperturbed) Hamiltonian H0, the eigenvalue problem for which is solved and the spectrum is continuous: The eigenstates form a complete orthonormal basis: What is the probability of finding the system at time t in a given group of states in a domain Df?

Coupling with the states of the continuous spectrum Introducing the density of final states ρ: Here β is the set of other parameters necessary to use if H0 is not a CSCO alone Then the probability of finding the system at time t in a given group of states is: