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Activities

Kinesthetic

10 min.

Acting Out Charge Densities
Students, pretending they are point charges, move around the room acting out various prompts from the instructor regarding charge densities, including linear \(\lambda\), surface \(\sigma\), and volume \(\rho\) charge densities, both uniform and non-uniform. The instructor demonstrates what it means to measure these quantities. In a remote setting, we have students manipulate 10 coins to model the prompts in this activity and we demonstrate the answers with coins under a doc cam.
In this lecture, the instructor guides a discussion about translating between bra-ket notation and wavefunction notation for quantum systems.

Kinesthetic

10 min.

Acting Out Current Density
Students, pretending they are point charges, move around the room so as to make an imaginary magnetic field meter register a constant magnetic field, introducing the concept of steady current. Students act out linear \(\vec{I}\), surface \(\vec{K}\), and volume \(\vec{J}\) current densities. The instructor demonstrates what it means to measure these quantities by counting how many students pass through a gate.

You have a charge distribution on the \(x\)-axis composed of two point charges: one with charge \(+3q\) located at \(x=-d\) and the other with charge \(-q\) located at \(x=+d\).

  1. Sketch the charge distribution.
  2. Write an expression for the volume charge density \(\rho (\vec{r})\) everywhere in space.

Computational Activity

120 min.

Mean position
Students compute probabilities and averages given a probability density in one dimension. This activity serves as a soft introduction to the particle in a box, introducing all the concepts that are needed.
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.

Small Group Activity

30 min.

Wavefunctions on a Quantum Ring
This activity lets students explore translating a wavefunction that isn't obviously made up of eigenstates at first glance into ket and matrix form. Then students explore wave functions, probabilities in a region, expectation values, and what wavefunctions can tell you about measurements of \(L_z\).

Problem

5 min.

Mass Density
Consider a rod of length \(L\) lying on the \(z\)-axis. Find an algebraic expression for the mass density of the rod if the mass density at \(z=0\) is \(\lambda_0\) and at \(z=L\) is \(7\lambda_0\) and you know that the mass density increases
  1. (2pts) linearly;
  2. (2pts) like the square of the distance along the rod;
  3. (2pts) exponentially.
  • Found in: AIMS Maxwell, Static Fields, Surfaces/Bridge Workshop, Problem-Solving course(s)

Problem

5 min.

Total Charge (HW)

For each case below, find the total charge.

  1. (4pts) A positively charged (dielectric) spherical shell of inner radius \(a\) and outer radius \(b\) with a spherically symmetric internal charge density \begin{equation*} \rho(\vec{r})=3\alpha\, e^{(kr)^3} \end{equation*}
  2. (4pts) A positively charged (dielectric) cylindrical shell of inner radius \(a\) and outer radius \(b\) with a cylindrically symmetric internal charge density \begin{equation*} \rho(\vec{r})=\alpha\, \frac{1}{s}\, e^{ks} \end{equation*}

Einstein condensation temperature Starting from the density of free particle orbitals per unit energy range \begin{align} \mathcal{D}(\varepsilon) = \frac{V}{4\pi^2}\left(\frac{2M}{\hbar^2}\right)^{\frac32}\varepsilon^{\frac12} \end{align} show that the lowest temperature at which the total number of atoms in excited states is equal to the total number of atoms is \begin{align} T_E &= \frac1{k_B} \frac{\hbar^2}{2M} \left( \frac{N}{V} \frac{4\pi^2}{\int_0^\infty\frac{\sqrt{\xi}}{e^\xi-1}d\xi} \right)^{\frac23} T_E &= \end{align} The infinite sum may be numerically evaluated to be 2.612. Note that the number derived by integrating over the density of states, since the density of states includes all the states except the ground state.

Note: This problem is solved in the text itself. I intend to discuss Bose-Einstein condensation in class, but will not derive this result.

Consider a white dwarf of mass \(M\) and radius \(R\). The dwarf consists of ionized hydrogen, thus a bunch of free electrons and protons, each of which are fermions. Let the electrons be degenerate but nonrelativistic; the protons are nondegenerate.

  1. Show that the order of magnitude of the gravitational self-energy is \(-\frac{GM^2}{R}\), where \(G\) is the gravitational constant. (If the mass density is constant within the sphere of radius \(R\), the exact potential energy is \(-\frac53\frac{GM^2}{R}\)).

  2. Show that the order of magnitude of the kinetic energy of the electrons in the ground state is \begin{align} \frac{\hbar^2N^{\frac53}}{mR^2} \approx \frac{\hbar^2M^{\frac53}}{mM_H^{\frac53}R^2} \end{align} where \(m\) is the mass of an electron and \(M_H\) is the mas of a proton.

  3. Show that if the gravitational and kinetic energies are of the same order of magnitude (as required by the virial theorem of mechanics), \(M^{\frac13}R \approx 10^{20} \text{g}^{\frac13}\text{cm}\).

  4. If the mass is equal to that of the Sun (\(2\times 10^{33}g\)), what is the density of the white dwarf?

  5. It is believed that pulsars are stars composed of a cold degenerate gas of neutrons (i.e. neutron stars). Show that for a neutron star \(M^{\frac13}R \approx 10^{17}\text{g}^{\frac13}\text{cm}\). What is the value of the radius for a neutron star with a mass equal to that of the Sun? Express the result in \(\text{km}\).

Problem

5 min.

Electric Field and Charge
Consider the electric field \begin{equation} \vec E(r,\theta,\phi) = \begin{cases} 0&\textrm{for } r<a\\ \frac{1}{4\pi\epsilon_0} \,\frac{Q}{b^3-a^3}\, \left( r-\frac{a^3}{r^2}\right)\, \hat r & \textrm{for } a<r<b\\ 0 & \textrm{for } r>b \\ \end{cases} \end{equation}
  1. (4pts) Use step and/or delta functions to write this electric field as a single expression valid everywhere in space.
  2. (4pts) Find a formula for the charge density that creates this electric field.
  3. (2pts) Interpret your formula for the charge density, i.e. explain briefly in words where the charge is.

One way to write volume charge densities without using piecewise functions is to use step \((\Theta)\) or \(\delta\) functions. Consider a spherical shell with charge density \[\rho (\vec{r})=\alpha3e^{(k r)^3} \]

between the inner radius \(a\) and the outer radius \(b\). The charge density is zero everywhere else.

  1. (2 pts) What are the dimensions of the constants \(\alpha\) and \(k\)?
  2. (2 pts) By hand, sketch a graph the charge density as a function of \(r\) for \(\alpha > 0\) and \(k>0\) .
  3. (2 pts) Use step functions to write this charge density as a single function valid everywhere in space.

Problem

5 min.

Volume Charge Density

Consider the volume charge density: \begin{equation*} \rho (x,y,z)=c\,\delta (x-3) \end{equation*}

  1. (2 pts) Describe in words how this charge is distributed in space.
  2. (2 pts) What are the dimensions of the constant \(c\)?

  • Found in: Static Fields, AIMS Maxwell, Problem-Solving course(s)

Problem

Cube Charge
  1. Charge is distributed throughout the volume of a dielectric cube with charge density \(\rho=\beta z^2\), where \(z\) is the height from the bottom of the cube, and where each side of the cube has length \(L\). What is the total charge inside the cube? Do this problem in two ways as both a single integral and as a triple integral.
  2. On a different cube: Charge is distributed on the surface of a cube with charge density \(\sigma=\alpha z\) where \(z\) is the height from the bottom of the cube, and where each side of the cube has length \(L\). What is the total charge on the cube? Don't forget about the top and bottom of the cube.
  • charge density
    Found in: Static Fields, AIMS Maxwell, Problem-Solving course(s) Found in: Integration Sequence sequence(s)
Students write python programs to compute the potential due to a square of surface charge, and then to visualize the result. This activity can be used to introduce students to the process of integrating numerically.

Students work in small groups to use the superposition principle \[V(\vec{r}) =\frac{1}{4\pi\epsilon_0}\int\frac{\rho(\vec{r}^{\,\prime})}{\vert \vec{r}-\vec{r}^{\,\prime}\vert} \, d\tau^{\prime}\] to find an integral expression for the electrostatic potential, \(V(\vec{r})\), everywhere in space, due to a ring of charge.

In an optional extension, students find a series expansion for \(V(\vec{r})\) either on the axis or in the plane of the ring, for either small or large values of the relevant geometric variable. Add an extra half hour or more to the time estimate for the optional extension.

Small Group Activity

30 min.

Total Charge
In this small group activity, students integrate over non-uniform charge densities in cylindrical and spherical coordinates to calculate total charge.

Small Group Activity

30 min.

The Pretzel
A pretzel is to be dipped in chocolate. The pretzel is in the shape of a quarter circle, consisting of a straight segment from the origin to the point (2,0), a circular arc from there to (0,2), followed by a straight segment back to the origin; all distances are in centimeters. The (linear) density of chocolate on the pretzel is given by \(\lambda = 3(x^ 2 + y^2 )\) in grams per centimeter. Find the total amount of chocolate on the pretzel.

Main ideas

  • Calculating (scalar) line integrals.
  • Use what you know!

Prerequisites

  • Familiarity with \(d\boldsymbol{\vec{r}}\).
  • Familiarity with “Use what you know” strategy.

Warmup

It is not necessary to explicitly introduce scalar line integrals, before this lab; figuring out that the (scalar) line element must be \(|d\boldsymbol{\vec{r}}|\) can be made part of the activity (if time permits).

Props

  • whiteboards and pens
  • “linear” chocolate covered candy (e.g. Pocky)

Wrapup

Emphasize that students must express each integrand in terms of a single variable prior to integration.

Emphasize that each integral must be positive!

Discuss several different ways of doing this problem (see below).


Details

In the Classroom

  • Make sure the shape of the pretzel is clear! It might be worth drawing it on the board.
  • Some students will work geometrically, determining \(ds\) on each piece by inspection. This is fine, but encourage such students to try using \(d\vec{r}\) afterwards.
  • Polar coordinates are natural for all three parts of this problem, not just the circular arc.
  • Many students will think that the integral “down” the \(y\)-axis should be negative. They will argue that \(ds=dy\), but the limits are from \(2\) to \(0\). The resolution is that \(ds = |dy\,\boldsymbol{\hat x}|=|dy|=-dy\) when integrating in this direction.
  • Unlike work or circulation, the amount of chocolate does not depend on which way one integrates, so there is in fact no need to integrate “down” the \(y\)-axis at all.
  • Some students may argue that \(d\boldsymbol{\vec{r}}=\boldsymbol{\hat T}\,ds\Longrightarrow ds=d\boldsymbol{\vec{r}}\cdot\boldsymbol{\hat T}\), and use this to get the signs right. This is fine if it comes up, but the unit tangent vector \(\boldsymbol{\hat T}\) is not a fundamental part of our approach.
  • There is of course a symmetry argument which says that the two “legs” along the axes must have the same amount of chocolate --- although some students will put a minus sign into this argument!

Subsidiary ideas

  • \(ds=|d\boldsymbol{\vec{r}}|\)

Small Group Activity

10 min.

Modeling Nonuniform Density
In this small group activity, students calculate a (linear) function to represent the charge density on a one-dimensional rod from a description of the charge density in words.
  • Found in: AIMS Maxwell, Static Fields, Surfaces/Bridge Workshop, Problem-Solving course(s)
With the Spins simulation set for a spin 1/2 system, measure the probabilities of all the possible spin components for each of the unknown initial states \(\left|{\psi_3}\right\rangle \) and \(\left|{\psi_4}\right\rangle \). (Since \(\left|{\psi_3}\right\rangle \) has already been covered in class, please only do \(\left|{\psi_4}\right\rangle \) )
  1. Use your measured probabilities to find each of the unknown states as a linear superposition of the \(S_z\)-basis states \(\left|{+}\right\rangle \) and \(\left|{-}\right\rangle \).
  2. Articulate a Process: Write a set of general instructions that would allow another student in next year's class to find an unknown state from measured probabilities.
  3. Compare Theory with Experiment: Design an experiment that will allow you to test whether your prediction for each of the unknown states is correct. Describe your experiment here, clearly but succinctly, as if you were writing it up for a paper. Do the experiment and discuss your results.
  4. Make a Conceptual Connection: In general, can you determine a quantum state with spin-component probability measurements in only two spin-component-directions? Why or why not?

Consider two noninteracting systems \(A\) and \(B\). We can either treat these systems as separate, or as a single combined system \(AB\). We can enumerate all states of the combined by enumerating all states of each separate system. The probability of the combined state \((i_A,j_B)\) is given by \(P_{ij}^{AB} = P_i^AP_j^B\). In other words, the probabilities combine in the same way as two dice rolls would, or the probabilities of any other uncorrelated events.

  1. Show that the entropy of the combined system \(S_{AB}\) is the sum of entropies of the two separate systems considered individually, i.e. \(S_{AB} = S_A+S_B\). This means that entropy is extensive. Use the Gibbs entropy for this computation. You need make no approximation in solving this problem.
  2. Show that if you have \(N\) identical non-interacting systems, their total entropy is \(NS_1\) where \(S_1\) is the entropy of a single system.

Note
In real materials, we treat properties as being extensive even when there are interactions in the system. In this case, extensivity is a property of large systems, in which surface effects may be neglected.

  1. \(\left\langle {\Psi}\middle|{\Psi}\right\rangle =1\) Identify and discuss the dimensions of \(\left|{\Psi}\right\rangle \).
  2. For a spin \(\frac{1}{2}\) system, \(\left\langle {\Psi}\middle|{+}\right\rangle \left\langle {+}\middle|{\Psi}\right\rangle + \left\langle {\Psi}\middle|{-}\right\rangle \left\langle {-}\middle|{\Psi}\right\rangle =1\). Identify and discuss the dimensions of \(\left|{+}\right\rangle \) and \(\left|{-}\right\rangle \).
  3. In the position basis \(\int \left\langle {\Psi}\middle|{x}\right\rangle \left\langle {x}\middle|{\Psi}\right\rangle dx = 1\). Identify and discuss the dimesions of \(\left|{x}\right\rangle \).

Problem

Phase 2
Consider the three quantum states: \[\left\vert \psi_1\right\rangle = \frac{4}{5}\left\vert +\right\rangle+ i\frac{3}{5} \left\vert -\right\rangle\] \[\left\vert \psi_2\right\rangle = \frac{4}{5}\left\vert +\right\rangle- i\frac{3}{5} \left\vert -\right\rangle\] \[\left\vert \psi_3\right\rangle = -\frac{4}{5}\left\vert +\right\rangle+ i\frac{3}{5} \left\vert -\right\rangle\]
  1. For each of the \(\left|{\psi_i}\right\rangle \) above, calculate the probabilities of spin component measurements along the \(x\), \(y\), and \(z\)-axes.
  2. Look For a Pattern (and Generalize): Use your results from \((a)\) to comment on the importance of the overall phase and of the relative phases of the quantum state vector.
A beam of spin-\(\frac{1}{2}\) particles is prepared in the initial state \[ \left\vert \psi\right\rangle = \sqrt{\frac{2}{5}}\; |+\rangle_x - \sqrt{\frac{3}{5}}\; |-\rangle_x \](Note: this state is written in the \(S_x\) basis!)
  1. What are the possible results of a measurement of \(S_x\), with what probabilities?
  2. Repeat part a for measurements of \(S_z\).

  3. Suppose you start with a particle in the state given above, measure \(S_x\), and happen to get \(+\hbar /2\). You then take that same particle and measure \(S_z\). What are the possible results and with what probability would you measure each possible result?

At low temperatures, a diatomic molecule can be well described as a rigid rotor. The Hamiltonian of such a system is simply proportional to the square of the angular momentum \begin{align} H &= \frac{1}{2I}L^2 \end{align} and the energy eigenvalues are \begin{align} E_{\ell m} &= \hbar^2 \frac{\ell(\ell+1)}{2I} \end{align}

  1. What is the energy of the ground state and the first and second excited states of the \(H_2\) molecule? i.e. the lowest three distinct energy eigenvalues.

  2. At room temperature, what is the relative probability of finding a hydrogen molecule in the \(\ell=0\) state versus finding it in any one of the \(\ell=1\) states?
    i.e. what is \(P_{\ell=0,m=0}/\left(P_{\ell=1,m=-1} + P_{\ell=1,m=0} + P_{\ell=1,m=1}\right)\)

  3. At what temperature is the value of this ratio 1?

  4. At room temperature, what is the probability of finding a hydrogen molecule in any one of the \(\ell=2\) states versus that of finding it in the ground state?
    i.e. what is \(P_{\ell=0,m=0}/\left(P_{\ell=2,m=-2} + P_{\ell=2,m=-1} + \cdots + P_{\ell=2,m=2}\right)\)

Kinesthetic

30 min.

Inner Products with Arms
Students perform an inner product between two spin states with the arms representation.

Small Group Activity

60 min.

Going from Spin States to Wavefunctions
Students review using the Arms representation to represent states for discrete quantum systems and connecting the Arms representation to histogram and matrix representation. The student then extend the Arms representation to begin exploring the continuous position basis.

Small Group Activity

30 min.

Working with Representations on the Ring
This activity acts as a reintroduction to doing quantum calculations while also introducing the matrix representation on the ring, allowing students to discover how to index and form a column vector representing the given quantum state. In addition, this activity introduces degenerate measurements on the quantum ring and examines the state after measuring both degenerate and non-degenerate eigenvalues for the state.
These notes, from the third week of https://paradigms.oregonstate.edu/courses/ph441 cover the canonical ensemble and Helmholtz free energy. They include a number of small group activities.

Lecture

120 min.

Gibbs entropy approach
These lecture notes for the first week of https://paradigms.oregonstate.edu/courses/ph441 include a couple of small group activities in which students work with the Gibbs formulation of the entropy.

Small Group Activity

30 min.

Superposition States for a Particle on a Ring
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.
Students calculate probabilities for energy, angular momentum, and position as a function of time for an initial state that is a linear combination of energy/angular momentum eigenstates for a particle confined to a ring written in bra-ket notation. This activity helps students build an understanding of when they can expect a quantity to depend on time and to give them more practice moving between representations.
Students calculate probabilities for a particle on a ring using three different notations: Dirac bra-ket, matrix, and wave function. After calculating the angular momentum and energy measurement probabilities, students compare their calculation methods for notation.
Students use Mathematica to visualize the probability density distribution for the hydrogen atom orbitals with the option to vary the values of \(n\), \(\ell\), and \(m\).
Students observe three different plots of linear combinations of spherical combinations with probability density represented by color on the sphere, distance from the origin (polar plot), and distance from the surface of the sphere.

Small White Board Question

5 min.

Normalization of the Gaussian for Wavefunctions
Students find a wavefunction that corresponds to a Gaussian probability density.
  • Found in: Periodic Systems course(s) Found in: Fourier Transforms and Wave Packets sequence(s)