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CRC Press eBooks

Time—Dependent Perturbation Theory

Şaki̇r Erkoç

Published Jul 28, 2006• 0 citations
Publisher

Abstract

Systems described by a time–independent potential energy function, V ( r , t ) = V ( r ), are the subject of quantum statics . Such systems may be studied by the time–dependent Schrödinger equation 16.1 H Ψ = i ℏ ∂ Ψ ∂ t https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9780429136528/397e01c1-e101-4a47-b552-a910642bbb8c/content/eqn16_1.tif"/>

DOI
10.1201/9781584887331-16

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Systems described by a time–independent potential energy function, V ( r , t ) = V ( r ), are the subject of quantum statics . Such systems may be studied by the time–dependent Schrödinger equation 16.1 H Ψ = i ℏ ∂ Ψ ∂ t https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9780429136528/397e01c1-e101-4a47-b552-a910642bbb8c/content/eqn16_1.tif"/>
In the previous chapter, we did not examine the change of a state with time https://www.w3.org/1998/Math/MathML"> t https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781003273073/d236e21f-f9f6-4e42-b186-ef1c50f0a68b/content/math2_1.tif" xmlns:xlink=" https://www.w3.org/1999/xlink "/> . It has been assumed that we have been examining a state at a given moment https://www.w3.org/1998/Math/MathML"> t https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781003273073/d236e21f-f9f6-4e42-b186-ef1c50f0a68b/content/math2_2.tif" xmlns:xlink=" https://www.w3.org/1999/xlink "/> . In the general case, the state of a system changes with time https://www.w3.org/1998/Math/MathML"> t https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781003273073/d236e21f-f9f6-4e42-b186-ef1c50f0a68b/content/math2_3.tif" xmlns:xlink=" https://www.w3.org/1999/xlink "/> . For example, say the motion of an electron in a potential field, its wave function depends on time https://www.w3.org/1998/Math/MathML"> t https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781003273073/d236e21f-f9f6-4e42-b186-ef1c50f0a68b/content/math2_4.tif" xmlns:xlink=" https://www.w3.org/1999/xlink "/> : https://www.w3.org/1998/Math/MathML"> Ψ = Ψ q , t https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781003273073/d236e21f-f9f6-4e42-b186-ef1c50f0a68b/content/math2_5.tif" xmlns:xlink=" https://www.w3.org/1999/xlink "/> . Such a dependence has to be described by a differential equation in which we may have https://www.w3.org/1998/Math/MathML"> ∂ Ψ ∂ t , ∂ 2 Ψ ∂ t 2 , ⋯ https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781003273073/d236e21f-f9f6-4e42-b186-ef1c50f0a68b/content/math2_6.tif" xmlns:xlink=" https://www.w3.org/1999/xlink "/> .
The solutions to the Time‐Independent Schrödinger Equation (TISE) can be found as long as we can define the Hamiltonian, which in the simplest cases, means defining the potential in which the particle of interest is moving. In the following sections, we will consider a single particle of mass, m p , moving in a potential that is time‐independent, but can vary in space. We will follow four steps: Define the Hamiltonian by defining the Potential Energy Operator since H ^ = - ħ 2 2 m p ∇ ^ 2 + V ^ ( r ) $ \hat{H} = - \frac{{{\hbar}^{2} }}{{2m_{p} }}\hat{\nabla }^{2} + \hat{V}(r) $ https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781315381381/5a219413-b541-4543-a0c3-fab4f5358e87/content/inline-math4_1.tif"/> . Solve the TISE to get the wave functions ψ ( x , y , z ) $ \psi (x, y, z) $ https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781315381381/5a219413-b541-4543-a0c3-fab4f5358e87/content/inline-math4_2.tif"/> and then the total stationary state wave functions Ψ ( x , y , z ; t ) = ψ ( x , y , z ) e - i ω t . $ \iPsi (x, y, z;t) = \psi (x, y, z)e^{ - i\omega t} . $ https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9781315381381/5a219413-b541-4543-a0c3-fab4f5358e87/content/inline-math4_3.tif"/> Determine the energies of the various states of the system. Examine the implications of the solutions to the Schrödinger equations.
Consider a two-level atom represented by the spin operators σ ^ ± , σ ^ Z , https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9780429092053/5e12ab0e-ba42-4caa-9bdf-6325e9117d3e/content/ineqn19_1.tif"/> interacting with a one-dimensional harmonic oscillator, represented by the creation and annihilation operators â † and â . The Hamiltonian of the system is given by ( 19.1 ) H ^ = 1 2 ℏ ω 0 σ ^ Z + ℏ w 0 ( a ^ † a ^ + 1 2 )− 1 2 i ℏ g + ( σ ^ + a ^ − σ ^ − a ^ † ) . https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9780429092053/5e12ab0e-ba42-4caa-9bdf-6325e9117d3e/content/eqn19_1.tif"/>
There are few potentials V (r) for which the Schrödinger equation is exactly solvable. We must therefore develop approximation techniques to obtain the eigenvalues and eigenfunctions for potentials that do not lead to exactly soluble equations. One of these methods is the perturbation theory, which was developed both for time independent and time dependent phenomena. We will discuss the time independent perturbation theory. The formulation of the time independent perturbation theory is different for nondegenerate and degenerate states.