## Quantum Particle in a 2-D Box

• face Quantum Reference Sheet

face Lecture

5 min.

##### Quantum Reference Sheet
Central Forces Spring 2021 Central Forces Spring 2021

assignment Homework

Energy and Entropy Fall 2020 Energy and Entropy Fall 2021

The isothermal compressibility is defined as $$K_{T}=-\frac{1}{V} \left(\frac{\partial V}{\partial p}\right)_{T}$$ $K_T$ is be found by measuring the fractional change in volume when the the pressure is slightly changed with the temperature held constant. In contrast, the adiabatic compressibility is defined as $$K_{S}=-\frac{1}{V} \left(\frac{\partial V}{\partial p}\right)_{S}$$ and is measured by making a slight change in pressure without allowing for any heat transfer. This is the compressibility, for instance, that would directly affect the speed of sound. Show that $$\frac{K_{T}}{K_{S}} = \frac{C_{p}}{C_{V}}$$ Where the heat capacities at constant pressure and volume are given by \begin{align} C_{p} &= T \left(\frac{\partial S}{\partial T}\right)_{p} \\ C_{V} &= T \left(\frac{\partial S}{\partial T}\right)_{V} \end{align}

• assignment Bottle in a Bottle 2

assignment Homework

##### Bottle in a Bottle 2
heat entropy ideal gas Energy and Entropy Fall 2020 Energy and Entropy Fall 2021

Consider the bottle in a bottle problem in a previous problem set, summarized here.

A small bottle of helium is placed inside a large bottle, which otherwise contains vacuum. The inner bottle contains a slow leak, so that the helium leaks into the outer bottle. The inner bottle contains one tenth the volume of the outer bottle, which is insulated.

The volume of the small bottle is 0.001 m23 and the volume of the big bottle is 0.01 m3. The initial state of the gas in the small bottle was $p=106$ Pa and its temperature $T=300$ K. Approximate the helium gas as an ideal gas of equations of state $pV=Nk_BT$ and $U=\frac32 Nk_BT$.

1. How many molecules of gas does the large bottle contain? What is the final temperature of the gas?

2. Compute the integral $\int \frac{{\mathit{\unicode{273}}} Q}{T}$ and the change of entropy $\Delta S$ between the initial state (gas in the small bottle) and the final state (gas leaked in the big bottle).

• assignment Potential vs. Potential Energy

assignment Homework

##### Potential vs. Potential Energy
AIMS Maxwell AIMS 21 Static Fields Winter 2021

In this course, two of the primary examples we will be using are the potential due to gravity and the potential due to an electric charge. Both of these forces vary like $\frac{1}{r}$, so they will have many, many similarities. Most of the calculations we do for the one case will be true for the other. But there are some extremely important differences:

1. Find the value of the electrostatic potential energy of a system consisting of a hydrogen nucleus and an electron separated by the Bohr radius. Find the value of the gravitational potential energy of the same two particles at the same radius. Use the same system of units in both cases. Compare and the contrast the two answers.
2. Find the value of the electrostatic potential due to the nucleus of a hydrogen atom at the Bohr radius. Find the gravitational potential due to the nucleus at the same radius. Use the same system of units in both cases. Compare and contrast the two answers.
3. Briefly discuss at least one other fundamental difference between electromagnetic and gravitational systems. Hint: Why are we bound to the earth gravitationally, but not electromagnetically?

• assignment Paramagnetism

assignment Homework

##### Paramagnetism
Energy Temperature Paramagnetism Thermal and Statistical Physics Spring 2020 Find the equilibrium value at temperature $T$ of the fractional magnetization $$\frac{\mu_{tot}}{Nm} \equiv \frac{2\langle s\rangle}{N}$$ of a system of $N$ spins each of magnetic moment $m$ in a magnetic field $B$. The spin excess is $2s$. The energy of this system is given by \begin{align} U &= -\mu_{tot}B \end{align} where $\mu_{tot}$ is the total magnetization. Take the entropy as the logarithm of the multiplicity $g(N,s)$ as given in (1.35 in the text): $$S(s) \approx k_B\log g(N,0) - k_B\frac{2s^2}{N}$$ for $|s|\ll N$, where $s$ is the spin excess, which is related to the magnetization by $\mu_{tot} = 2sm$. Hint: Show that in this approximation $$S(U) = S_0 - k_B\frac{U^2}{2m^2B^2N},$$ with $S_0=k_B\log g(N,0)$. Further, show that $\frac1{kT} = -\frac{U}{m^2B^2N}$, where $U$ denotes $\langle U\rangle$, the thermal average energy.
• assignment Visualization of Wave Functions on a Ring

assignment Homework

##### Visualization of Wave Functions on a Ring
Central Forces Spring 2021 Using either this Geogebra applet or this Mathematica notebook, explore the wave functions on a ring. (Note: The Geogebra applet may be a little easier to use and understand and is accessible if you don't have access to Mathematica, but it is more limited in the wave functions that you can represent. Also, the animation is pretty jumpy in some browsers, especially Firefox. Imagine that the motion is smooth.)
1. Look at graphs of the following states \begin{align} \Phi_1(\phi)&=\frac{1}{\sqrt{2}}(\left|{2}\right\rangle +\left|{-2}\right\rangle )\\ \Phi_2(\phi)&=\frac{1}{\sqrt{2}}(\left|{2}\right\rangle -\left|{-2}\right\rangle )\\ \Phi_3(\phi)&=\frac{1}{\sqrt{2}}(\left|{2}\right\rangle +i\left|{-2}\right\rangle ) \end{align} Write a short description of how these states differ from each other.
2. Find a state for which the probability density does not depend on time. Write the state in both ket and wave function notation. These are called stationary states. Generalize your result to give a characterization of the set of all possible states that are stationary states.
3. Find a state that is right-moving. Write the state in both ket and wave function notation. Generalize your result to give a characterization of the set of all possible states that are right-moving.
4. Find a state that is a standing wave. Write the state in both ket and wave function notation. Generalize your result to give a characterization of the set of all possible states that are standing waves.
• group Operators & Functions

group Small Group Activity

30 min.

##### Operators & Functions
Quantum Fundamentals Winter 2021 Students are asked to:
• Test to see if one of the given functions is an eigenfunction of the given operator
• See if they can write the functions that are found not to be eigenfunctions as a linear combination of eigenfunctions.
• accessibility_new Using Arms to Represent Time Dependence in Spin 1/2 Systems

accessibility_new Kinesthetic

10 min.

##### Using Arms to Represent Time Dependence in Spin 1/2 Systems

Arms Sequence for Complex Numbers and Quantum States

Students, working in pairs, use their left arms to demonstrate time evolution in spin 1/2 quantum systems.
• computer Visualization of Quantum Probabilities for a Particle Confined to a Ring

computer Mathematica Activity

30 min.

##### Visualization of Quantum Probabilities for a Particle Confined to a Ring
Central Forces Spring 2021

Quantum Ring Sequence

Students see probability density for eigenstates and linear combinations of eigenstates for a particle on a ring. The three visual representations: standard position vs probability density plot, a ring with colormapping, and cylindrical plot with height and colormapping, are also animated to visualize time-evolution.
• group Superposition States for a Particle on a Ring

group Small Group Activity

30 min.

##### Superposition States for a Particle on a Ring

Quantum Ring Sequence

Students calculate probabilities for a particle on a ring whose wavefunction is not easily separated into eigenstates by inspection. To find the energy, angular momentum, and position probabilities, students perform integrations with the wavefunction or decompose the wavefunction into a superposition of eigenfunctions.
• Central Forces Spring 2021

(2 points each)

You know that the normalized spatial eigenfunctions for a particle in a 1-D box of length $L$ are $\sqrt{\frac{2}{L}}\sin{\frac{n\pi x}{L}}$. If you want the eigenfunctions for a particle in a 2-D box, then you just multiply together the eigenfunctions for a 1-D box in each direction. (This is what the separation of variables procedure tells you to do.)

1. Find the normalized eigenfunctions for a particle in a 2-D box with sides of length $L_x$ in the $x$-direction and length $L_y$ in the $y$-direction.
2. Find the Hamiltonian for a 2-D box and show that your eigenstates are indeed eigenstates and find a formula for the possible energies
3. Any sufficiently smooth spatial wave function inside a 2-D box can be expanded in a double sum of the product wave functions, i.e. $$\psi(x,y)=\sum_{n=1}^{\infty}\sum_{m=1}^{\infty}\, c_{nm}\; \hbox{eigenfunction}_n(x)\;\hbox{eigenfunction}_m(y)$$ Using your expressions from part (a) above, write out all the terms in this sum out to $n=3$, $m=3$. Arrange the terms, conventionally, in terms of increasing energy.

You may find it easier to work in bra/ket notation: \begin{align*} \left|{\psi}\right\rangle &=\sum_{n=1}^{\infty}\sum_{m=1}^{\infty}\, c_{nm}\left|{n}\right\rangle \left|{m}\right\rangle \\ &=\sum_{n=1}^{\infty}\sum_{m=1}^{\infty}\, c_{nm}\left|{nm}\right\rangle \end{align*}

4. Find a formula for the $c_{nm}$s in part (b). Find the formula first in bra ket notation and then rewrite it in wave function notation.