Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

Consider an electron that is confined to a one-dimensional infinite potential well of width \(a=0.10 \mathrm{nm},\) and another electron that is confined to a three-dimensional (cubic) infinite potential well with sides of length \(a=0.10 \mathrm{nm}\). Let the electron confined to the cube be in its ground state. Determine the difference in energy ground state of the two electrons and the excited state of the one-dimensional electron that minimizes the difference in energy with the three-dimensional electron.

Short Answer

Expert verified
Answer: The excited state for the 1D electron that minimizes the difference in energy with the 3D electron has a quantum number of 2 (n'=2).

Step by step solution

01

Finding the energy ground state for 1D electron

We have a one-dimensional infinite potential well of width \(a = 0.10\) nm, and for the lowest energy ground state, we set the energy quantum number \(n = 1\). To find the energy for this electron, we plug these values into the 1D energy formula: \(E_{1D} = \frac{(1)^2 \pi^2 \hbar^2}{2m(0.10 \times 10^{-9})^2}\) Calculating the energy, we get: \(E_{1D} = 6.024\times10^{-20} J\)
02

Finding the energy ground state for 3D electron

The electron is confined to a three-dimensional cubical well with sides of length \(a = 0.10\) nm. For the lowest energy ground state, we set the energy quantum numbers \(n_x = n_y = n_z = 1\). Plugging these values into the 3D energy formula: \(E_{3D} = \frac{(1^2+1^2+1^2)\pi^2\hbar^2}{2m(0.10\times10^{-9})^2}\) Calculating the energy, we get: \(E_{3D} = 1.807\times10^{-19} J\)
03

Determine the difference in energy ground states

Now, we will find the difference in energy ground states between the 1D and 3D electrons: \(\Delta E = E_{3D} - E_{1D} = 1.807\times10^{-19} J - 6.024\times10^{-20} J\) \(\Delta E = 1.205\times10^{-19} J\)
04

Finding the excited state for 1D electron

We need to find the excited state (\(n'\)) of the 1D electron which minimizes the difference in energy with the ground state energy of the 3D electron. Using the energy formula for the 1D electron: \(E'_{1D} = \frac{{n'}^2\pi^2\hbar^2}{2ma^2}\) We need to minimize the difference: \(\Delta E = |E_{3D} - E'_{1D}| = |1.807\times10^{-19} J - \frac{{n'}^2\pi^2\hbar^2}{2m(0.10\times10^{-9})^2}|\) To minimize the difference, we need a value of \(n'\) such that: \(n'^2 = \frac{2m(0.10\times10^{-9})^2}{\pi^2\hbar^2}(E_{3D}-E_{1D})\) Plugging the values of energy from previous steps, and calculating \(n'\): \(n' = \sqrt{\frac{2(9.109\times10^{-31}\,\text{kg})(0.10\times10^{-9}\,\text{m})^2}{\pi^2(1.055\times10^{-34}\,\text{J s})^2}(1.205\times10^{-19}\,\text{J})} \approx 1.87\) As we can't have fractional quantum numbers, we round up \(n'\) to the nearest integer. So, the closest excited state for the 1D electron is: \(n' = 2\) The strategy to find the excited state involves finding the \(n'\) value that would make the energy difference between the 1D and the 3D electron as close as possible. This allowed us to determine that an excited state with a quantum number of 2 would minimize this difference.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

In the cores of white dwarf stars, carbon nuclei are thought to be locked into very ordered lattices because the temperature is quite cold, $\sim 10^{4} \mathrm{~K}$. Consider the case of a onedimensional lattice of carbon atoms separated by \(20 \mathrm{fm}\) ( \(1 \mathrm{fm}=\) $1 \cdot 10^{-15} \mathrm{~m}$ ). Consider the central atom of a row of three atoms with this spacing. Approximate the Coulomb potentials of the two outside atoms to follow a quadratic relationship, assuming small vibrations; what energy state would the central carbon atom be in at this temperature? (Use $E=3 / 2 k_{\mathrm{B}} T$.)

Is the following statement true or false? The larger the amplitude of a Schrödinger wave function, the larger its kinetic energy. Explain your answer.

Consider a square potential, \(U(x)=0\) for \(x<-\alpha, U(x)=-U_{0}\) for \(-\alpha \leq x \leq \alpha,\) where \(U_{0}\) is a positive constant, and \(U(x)=0\) for \(x>\alpha .\) For \(E>0,\) the solutions of the time-independent Schrödinger equation in the three regions will be the following: For \(x<-\alpha, \psi(x)=e^{i \kappa x}+R e^{-i \kappa x},\) where \(\kappa^{2}=2 m E / \hbar^{2}\) and \(R\) is the amplitude of a reflected wave. For \(-\alpha \leq x \leq \alpha, \psi(x)=A e^{i \kappa^{\prime} x}+B e^{-i \kappa^{\prime} x},\) and \(\left(\kappa^{\prime}\right)^{2}=2 m\left(E+U_{0}\right) / \hbar^{2}\) For \(x>\alpha, \psi(x)=T e^{i \kappa x}\) where \(T\) is the amplitude of the transmitted wave. Match \(\psi(x)\) and \(d \psi(x) / d x\) at \(-\alpha\) and \(\alpha\) and find an expression for \(R\). What is the condition for which \(R=0\) (that is, there is no reflected wave)?

An oxygen molecule has a vibrational mode that behaves approximately like a simple harmonic oscillator with frequency \(2.99 \cdot 10^{14} \mathrm{rad} / \mathrm{s} .\) Calculate the energy of the ground state and the first two excited states.

Write a wave function \(\Psi(\vec{r}, t)\) for a nonrelativistic free particle of mass \(m\) moving in three dimensions with momentum \(\vec{p}\), including the correct time dependence as required by the Schrödinger equation. What is the probability density associated with this wave?

See all solutions

Recommended explanations on Physics Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free