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A particle of mass \(m\) in a one-dimensional box has the following wave function in the region \(x=0\) to \(x=L:\) $$\Psi(x, t)=\frac{1}{\sqrt{2}} \psi_{1}(x) e^{-i E_{1} t / \hbar}+\frac{1}{\sqrt{2}} \psi_{3}(x) e^{-i E_{3} t / \hbar}$$ Here \(\psi_{1}(x)\) and \(\psi_{3}(x)\) are the normalized stationary-state wave functions for the \(n=1\) and \(n=3\) levels, and \(E_{1}\) and \(E_{3}\) are the energies of these levels. The wave function is zero for \(x<0\) and for \(x>L\) (a) Find the value of the probability distribution function at \(x=L / 2\) as a function of time. (b) Find the angular frequency at which the probability distribution function oscillates.

Short Answer

Expert verified
The value of the probability distribution function at \(x=L / 2\) as a function of time oscillates with an angular frequency of \((E3 - E1) / \hbar\).

Step by step solution

01

Set up the problem

Observe that the initial wavefunction of the particle is given as a superposition of the first and third energy eigenstates. Therefore, the time-dependent wavefunction for a particle in a box can be represented as \(\Psi(x, t)=\frac{1}{\sqrt{2}} \psi_{1}(x) e^{-i E_{1} t / \hbar}+\frac{1}{\sqrt{2}} \psi_{3}(x) e^{-i E_{3} t / \hbar}\). The states \(\psi_1\) and \(\psi_3\) are normalized stationary-state wave functions for the \(n=1\) and \(n=3\) levels, and \(E_{1}\) and \(E_{3}\) are the energies of these levels. From quantum mechanics, we know that \(\psi_n(x)=\sqrt{2/L}\sin(n\pi x/L)\) and \(E_n=n^2\pi^2\hbar^2/2mL^2\).
02

Find the probability distribution function

The probability distribution function \(P\) is given by \(P = |\Psi|^2\). So we need to find \(\Psi^*\Psi\) at \(x = L/2\) where \(\Psi^*\) is complex conjugate of \(\Psi\). Substitute the values for \(\psi_n(x)\) and \(E_n\) into \(\Psi\), calculate \(\Psi^*\), and then calculate \(\Psi^*\Psi\) at \(x = L/2\).
03

Determine angular frequency

The angular frequency of such a system can be obtained by looking for a term in \(\Psi^*\Psi\) which has the form of a sinusoidal function. In this case, that term is proportional to \(\cos((E3 - E1)t / \hbar)\). Therefore, the angular frequency \(\omega\) is the coefficient of \(t\) in the argument of the cosine function, which equates to \((E3 - E1) / \hbar\).

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Key Concepts

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

Wave Function
The concept of a wave function is at the heart of quantum mechanics. It's a powerful mathematical expression used to describe the quantum state of a particle. In essence, the wave function, usually denoted by the Greek letter \( \Psi \), encapsulates all the information about a particle's position and momentum.

In the one-dimensional box scenario, the wave function \( \Psi(x, t) \) for a particle is constructed from the pure energy states \( \psi_n(x) \), which describe the particle's position, and time-dependent factors that account for its energy state evolution. Each possible state \( \psi_n(x) \) corresponds to a specific energy level, which, when combined, give a complete description of the quantum state of the particle.

Understanding a particle's wave function is crucial, as it allows us to predict the likelihood of finding the particle at a particular position and time. This leads us to another foundational concept in quantum mechanics: the probability distribution function.
Probability Distribution Function
The probability distribution function is a square of the magnitude of the wave function, represented by \( P = |\Psi|^2 \). This function provides the probability density of finding a particle at various positions within the box at any given time.

Intuitively, the wave function can sometimes be complex, having both real and imaginary parts. Consequently, to obtain a real number that is interpretable as a probability, we need to multiply the wave function by its complex conjugate, leading to the probability distribution function. For example, at the midpoint of the box, \( x = L/2 \), we find the probability of locating the particle there by evaluating \( P \) at that specific point.

This concept is critical in quantum mechanics, as it transitions the abstract notion of a wave function into something more tangible: the likelihood of an observable event, which is a key insight when predicting and understanding quantum phenomena.
Quantum States
Quantum states are the distinct, allowable configurations of a quantum system, each associated with a specific energy level. They are described by the stationary-state wave functions \( \psi_n(x) \). In the context of a particle in a box, these states are quantized, meaning that only specific energy values are permitted.

The quantization arises from the constraints imposed on the particle: it can't exist outside the box, leading to boundary conditions that the wave function must satisfy. For a particle in a one-dimensional box, the stationary states are sinusoidal functions shaped according to the box's length \( L \).

The concept of quantum states is significant in understanding the arrangement and behavior of particles in confined spaces. In the exercise given, the particle can inhabit either the first (\( n=1 \)) or third (\( n=3 \)) energy level, and the superposition of these states creates a complex system that evolves over time.
Angular Frequency
Angular frequency, denoted as \( \omega \), is a measure of how rapidly the probability distribution function of a quantum system oscillates in time. This concept is linked to the energy difference between quantum states and helps determine the dynamism of superposition states.

In the particle in a box scenario, angular frequency quantifies the oscillation rate of the probability to find the particle at a certain position within the box. In the exercise, it is derived from the difference in energy levels of the superposed states \( E3 \) and \( E1 \), as part of the term \( \cos((E3 - E1)t / \hbar) \) found in the expression for \( P \).

Understanding angular frequency is vital as it gives insight into the time-based behavior of quantum systems and allows us to predict the rate at which quantum states change over time, a phenomenon directly observable in phenomena such as electron transitions and the emission of photons.

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Most popular questions from this chapter

The penetration distance \(\eta\) in a finite potential well is the distance at which the wave function has decreased to \(1 / e\) of the (b) wave function at the classical turning point: $$ \psi(x=L+\eta)=\frac{1}{e} \psi(L) $$ The penetration distance can be shown to be $$\eta=\frac{\hbar}{\sqrt{2 m\left(U_{0}-E\right)}}$$ The probability of finding the particle beyond the penetration distance is nearly zero. (a) Find \(\eta\) for an electron having a kinetic energy of \(13 \mathrm{eV}\) in a potential well with \(U_{0}=20 \mathrm{eV} .\) (b) Find \(\eta\) for a \(20.0 \mathrm{MeV}\) proton trapped in a 30.0 -MeV-deep potential well.

The WKB Approximation. It can be a challenge to solve the Schrödinger equation for the bound-state energy levels of an arbitrary potential well. An alternative approach that can yield good approximate results for the energy levels is the \(W K B\) approximation (named for the physicists Gregor Wentzel, Hendrik Kramers, and Léon Brillouin, who pioneered its application to quantum mechanics). The WKB approximation begins from three physical statements: (i) According to de Broglie, the magnitude of momentum \(p\) of a quantum-mechanical particle is \(p=h / \lambda\). (ii) The magnitude of momentum is related to the kinetic energy \(K\) by the relationship \(K=p^{2} / 2 m .\) (iii) If there are no nonconservative forces, then in Newtonian mechanics the energy \(E\) for a particle is constant and equal at each point to the sum of the kinetic and potential energies at that point: \(E=K+U(x),\) where \(x\) is the coordinate. (a) Combine these three relationships to show that the wavelength of the particle at a coordinate \(x\) can be written as $$ \lambda(x)=\frac{h}{\sqrt{2 m[E-U(x)]}} $$ Thus we envision a quantum- mechanical particle in a potential well \(U(x)\) as being like a free particle, but with a wavelength \(\lambda(x)\) that is a function of position. (b) When the particle moves into a region of increasing potential energy, what happens to its wavelength? (c) At a point where \(E=U(x),\) Newtonian mechanics says that the particle has zero kinetic energy and must be instantaneously at rest. Such a point is called a classical turning point, since this is where a Newtonian particle must stop its motion and reverse direction. As an example, an object oscillating in simple harmonic motion with amplitude \(A\) moves back and forth between the points \(x=-A\) and \(x=+A ;\) each of these is a classical turning point, since there the potential energy \(\frac{1}{2} k^{\prime} x^{2}\) equals the total energy \(\frac{1}{2} k^{\prime} A^{2}\). In the WKB expression for \(\lambda(x),\) what is the wavelength at a classical turning point? (d) For a particle in a box with length \(L,\) the walls of the box are classical turning points (see Fig. 40.8\()\) Furthermore, the number of wavelengths that fit within the box must be a half-integer (see Fig. 40.10 ), so that \(L=(n / 2) \lambda\) and hence \(L / \lambda=n / 2,\) where \(n=1,2,3, \ldots\) [Note that this is a restatement of Eq. (40.29).] The WKB scheme for finding the allowed bound-state energy levels of an arbitrary potential well is an extension of these observations. It demands that for an allowed energy \(E\), there must be a half-integer number of wavelengths between the classical turning points for that energy. Since the wavelength in the WKB approximation is not a constant but depends on \(x\), the number of wavelengths between the classical turning points \(a\) and \(b\) for a given value of the energy is the integral of \(1 / \lambda(x)\) between those points: $$ \int_{a}^{b} \frac{d x}{\lambda(x)}=\frac{n}{2} \quad(n=1,2,3, \ldots) $$ Using the expression for \(\lambda(x)\) you found in part (a), show that the \(W K B\) condition for an allowed bound-state energy can be written as $$ \int_{a}^{b} \sqrt{2 m[E-U(x)]} d x=\frac{n h}{2} \quad(n=1,2,3, \ldots) $$ (e) As a check on the expression in part (d), apply it to a particle in a box with walls at \(x=0\) and \(x=L\). Evaluate the integral and show that the allowed energy levels according to the WKB approximation are the same as those given by Eq. (40.31). (Hint: since the walls of the box are infinitely high, the points \(x=0\) and \(x=L\) are classical turning points for any energy \(E .\) Inside the box, the potential energy is zero.) (f) For the finite square well shown in Fig. \(40.13,\) show that the \(\mathrm{WKB}\) expression given in part (d) predicts the same bound-state energies as for an infinite square well of the same width. (Hint: Assume \(E

An electron is bound in a square well that has a depth equal to six times the ground-level energy \(E_{1-\mathrm{IDW}}\) of an infinite well of the same width. The longest-wavelength photon that is absorbed by this electron has a wavelength of \(582 \mathrm{nm}\). Determine the width of the well.

Consider a potential well defined as \(U(x)=\infty\) for \(x<0, U(x)=0 \quad\) for \(\quad 00\) for \(x>L\) (Fig. \(\mathbf{P 4 0 . 5 8}\) ). Consider a particle with mass \(m\) and kinetic energy \(EL\) be in order to satisfy both the Schrödinger equation and this boundary condition at infinity? (c) Impose the boundary conditions that \(\psi\) and \(d \psi / d x\) are continuous at \(x=L\). Show that the energies of the allowed levels are obtained from solutions of the equation \(k \cot k L=-\kappa,\) where \(k=\sqrt{2 m E} / \hbar\) and \(\kappa=\sqrt{2 m\left(U_{0}-E\right)} / \hbar\)

(a) Find the excitation energy from the ground level to the third excited level for an electron confined to a box of width \(0.360 \mathrm{nm}\). (b) The electron makes a transition from the \(n=1\) to \(n=4\) level by absorbing a photon. Calculate the wavelength of this photon.

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