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The unperturbed Hamiltonian of a two-state system is represented by $$ H_{0}=\left(\begin{array}{cc} E_{1}^{0} & 0 \\ 0 & E_{2}^{0} \end{array}\right) \text {. } $$ There is, in addition, a time-dependent perturbation $$ V(t)=\left(\begin{array}{cc} 0 & \lambda \cos \omega t \\ \lambda \cos \omega t & 0 \end{array}\right) \quad(\lambda \mathrm{real}) $$ a. At \(t=0\) the system is known to be in the first state, represented by $$ \left(\begin{array}{l} 1 \\ 0 \end{array}\right) $$ Using time-dependent perturbation theory and assuming that \(E_{1}^{0}-E_{2}^{0}\) is not close to \(\pm \hbar \omega\), derive an expression for the probability that the system be found in the second state represented by $$ \left(\begin{array}{l} 0 \\ 1 \end{array}\right) $$ as a function of \(t(t>0)\). b. Why is this procedure not valid when \(E_{1}^{0}-E_{2}^{0}\) is close to \(\pm \hbar \omega\) ?

Short Answer

Expert verified
The probability expression involves integrals with frequency terms; it's invalid at resonance due to divergence.

Step by step solution

01

Understanding the Problem

We need to find the probability that a system initially in state \( \left(\begin{array}{l} 1 \ 0 \end{array}\right) \) transitions to state \( \left(\begin{array}{l} 0 \ 1 \end{array}\right) \) due to a time-dependent perturbation \( V(t) \), using time-dependent perturbation theory.
02

Determining the Perturbation Theory Approach

Using time-dependent perturbation theory, the first-order probability amplitude for transitioning from state \( |1\rangle \) (initial) to state \( |2\rangle \) (final) is given by:\[c_{2}^{(1)}(t) = -\frac{i}{\hbar} \int_{0}^{t} e^{i \omega_{21} t'} V_{21}(t') dt'\]where \( \omega_{21} = \frac{E_2^0 - E_1^0}{\hbar} \) and \( V_{21}(t) = \lambda \cos(\omega t) \).
03

Calculating the Integral

Substitute \( V_{21}(t) = \lambda \cos(\omega t) \) into the integral.\[c_{2}^{(1)}(t) = -\frac{i \lambda}{\hbar} \int_{0}^{t} e^{i \omega_{21} t'} \cos(\omega t') dt'\]Utilize the identity \( \cos(\omega t') = \frac{1}{2}(e^{i \omega t'} + e^{-i \omega t'}) \) to split this into two separate integrals.
04

Solve the Integrals Separately

The integral becomes the sum of two exponential integrals:\[c_{2}^{(1)}(t) = -\frac{i \lambda}{2 \hbar} \left( \int_{0}^{t} e^{i(\omega_{21} + \omega)t'} dt' + \int_{0}^{t} e^{i(\omega_{21} - \omega)t'} dt' \right)\]Compute each integral separately:\[\int e^{i\alpha t'} dt' = \frac{e^{i\alpha t'}}{i\alpha}\]
05

Evaluate the Integrals at Boundaries

For each integral,\[\int_{0}^{t} e^{i(\omega_{21} + \omega)t'} dt' = \frac{1}{i(\omega_{21} + \omega)} \left( e^{i(\omega_{21} + \omega)t} - 1 \right)\]\[\int_{0}^{t} e^{i(\omega_{21} - \omega)t'} dt' = \frac{1}{i(\omega_{21} - \omega)} \left( e^{i(\omega_{21} - \omega)t} - 1 \right)\]
06

Combine Results into Transition Amplitude

Substitute these results back into the expression for \( c_{2}^{(1)}(t) \) and simplify:\[c_{2}^{(1)}(t) = \frac{\lambda}{2\hbar} \left( \frac{ e^{i(\omega_{21} + \omega)t} - 1 }{ \omega_{21} + \omega } + \frac{ e^{i(\omega_{21} - \omega)t} - 1 }{ \omega_{21} - \omega } \right)\]
07

Calculate the Transition Probability

The probability of finding the system in state \( |2\rangle \) is the modulus squared of the transition amplitude:\[P_{1\rightarrow 2}(t) = \left| c_{2}^{(1)}(t) \right|^2\]
08

Addressing Energy Level Conditions

This procedure becomes invalid when \( E_{1}^{0} - E_{2}^{0} \approx \pm \hbar \omega \) due to the resonance condition, causing denominators in \( c_{2}^{(1)}(t) \) to approach zero and making the perturbative approach insufficient.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Two-State System
A two-state system is a simple quantum mechanical model that describes a system with exactly two possible states or configuration. This model is often used because it's simple yet meaningful, providing insight into more complex quantum phenomena.
In the context of this exercise, the two-state system is represented as a 2x2 matrix with
  • two energy eigenstates, each associated with specific energy levels \( E_1^0 \) and \( E_2^0 \).
  • The initial state of the system is the first energy level, depicted as \( \left( \begin{array}{c} 1 \ 0 \end{array} \right) \), which implies full occupancy of the first state and none in the second.
Understanding this simple model helps in analyzing how quantum mechanical systems evolve over time, focusing on how a system transitions between these states.
Quantum Mechanics
Quantum mechanics is the branch of physics dealing with the behavior of systems on very small scales, such as atoms and subatomic particles. It is a foundational theory that describes nature at the smallest scales of energy levels.
  • It works with probabilities instead of certainties, giving rise to phenomena like superposition and entanglement.
  • In a quantum system, particles do not have definite positions or velocities until they are observed.
In this exercise, quantum mechanics enables the investigation into how a quantum system, specifically a two-state system, behaves under a time-dependent perturbation, and how the likelihood of different states changes with time. The probabilistic nature of quantum mechanics requires the use of probability amplitudes and integrals, as in the provided solution, to determine the outcome of quantum transitions.
Hamiltonian Operator
The Hamiltonian operator in quantum mechanics represents the total energy of the system, including kinetic and potential energy. It plays a crucial role in determining the evolution of a quantum system, as it is central to the Schrödinger equation.
In our two-state system, the Hamiltonian is represented by
  • an initial, unperturbed Hamiltonian \( H_0 \) with diagonal elements \( E_1^0 \) and \( E_2^0 \), indicating energies of the states without perturbation.
  • a time-dependent perturbation \( V(t) \) that introduces a coupling between the states, modulated by \( \lambda \cos \omega t \).
This perturbation essentially shifts the energies of the states over time, leading to the possibility of transitions between states. The Hamiltonian operator is thus the tool used to determine these transitions as well as the overall dynamics of the quantum system.
Transition Probability
In quantum mechanics, transition probability refers to the probability that a system will transition from one state to another over time when subjected to a perturbation. It is a critical concept for understanding how quantum states evolve, especially under influence of external forces or fields.
In this context:
  • We seek the probability of the system transitioning from state \( |1\rangle \) to state \( |2\rangle \).
  • This involves calculating the transition amplitude, which is a complex number, and then squaring its magnitude to obtain the transition probability.
  • The result shows how likely the system is found in the second state after time \( t \).
The exercise uses first-order time-dependent perturbation theory to derive this probability, but notes that the theory becomes problematic in cases of near-resonance, where the energy difference \( E_1^0 - E_2^0 \) approaches \( \pm \hbar \omega \). Here, the approximation may lead to inaccuracies due to resonance effects amplifying the transition.

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Most popular questions from this chapter

This chapter derived two of the three relativistic corrections to the one- electron atom, namely \(\Delta_{K}^{(1)}\) from "relativistic kinetic energy," and \(\Delta_{L S}^{(1)}\) from the spin-orbit interaction. A third term comes from the spread of the electron wave function in the region of changing electric field. The perturbation for this "Darwin term" is $$ V_{D}=-\frac{1}{8 m^{2} c^{2}} \sum_{i=1}^{3}\left[p_{i},\left[p_{i}, e \phi(r)\right]\right] $$ where \(\phi(r)\) is the Coulomb potential. Find \(\Delta_{D}^{(1)}\) and show that $$ \Delta_{n j}^{(1)} \equiv \Delta_{K}^{(1)}+\Delta_{L S}^{(1)}+\Delta_{D}^{(1)}=\frac{m c^{2}(Z \alpha)^{4}}{2 n^{3}}\left[\frac{3}{4 n}-\frac{1}{j+1 / 2}\right] . $$ In Section \(8.4\) we will compare this expression to the result of solving the Dirac equation in the presence of the Coulomb potential.

Consider a particle in one dimension moving under the influence of some timeindependent potential. The energy levels and the corresponding eigenfunctions for this problem are assumed to be known. We now subject the particle to a traveling pulse represented by a time-dependent potential, $$ V(t)=A \delta(x-c t) . $$ a. Suppose at \(t=-\infty\) the particle is known to be in the ground state whose energy eigenfunction is \(\langle x \mid i\rangle=u_{i}(x)\). Obtain the probability for finding the system in some excited state with energy eigenfunction \(\langle x \mid f\rangle=u_{f}(x)\) at \(t=+\infty\). b. Interpret your result in (a) physically by regarding the \(\delta\)-function pulse as a superposition of harmonic perturbations; recall $$ \delta(x-c t)=\frac{1}{2 \pi c} \int_{-\infty}^{\infty} d \omega e^{i \omega[(x / c)-t]} . $$ Emphasize the role played by energy conservation, which holds even quantum mechanically as long as the perturbation has been on for a very long time.

A one-dimensional potential well has infinite walls at \(x=0\) and \(x=L\). The bottom of the well is not flat, but rather increases linearly from 0 at \(x=0\) to \(V\) at \(x=L\). Find the first-order shift in the energy levels as a function of principal quantum number \(n\).

Consider the spontaneous emission of a photon by an excited atom. The process is known to be an \(E 1\) transition. Suppose the magnetic quantum number of the atom decreases by one unit. What is the angular distribution of the emitted photon? Also discuss the polarization of the photon with attention to angular- momentum conservation for the whole (atom plus photon) system.

A simple harmonic oscillator (in one dimension) is subjected to a perturbation $$ H_{1}=b x $$ where \(b\) is a real constant. a. Calculate the energy shift of the ground state to lowest nonvanishing order. b. Solve this problem exactly and compare with your result obtained in (a).

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