2. Consider a classical particle moving in a one-dimensional potential well u(x), as shown The particle is in thermal equilibrium with a reservoir at temperature T, so the probabilities of its various states are determined by Boltzmann statistics.

{a) Show that the average position of the particle is given by

where each integral is over the entire xaxis.

A one-dimensional potential well. The higher the temperature, the farther the particle will stray from the equilibrium point.

(b) If the temperature is reasonably low (but still high enough for classical mechanics to apply), the particle will spend most of its time near the bottom of the potential well. In that case we can expand u(x)in a Taylor series about the equilibrium point x0: u(x)=ux0+x-x0dudxx0+12x-x02d2udx2x0

+13!x-x03d3udx3x0+

Show that the linear term must be zero, and that truncating the series after the quadratic term results in the trivial prediction x=x0.

(c) If we keep the cubic term in the Taylor series as well, the integrals in the formula for xbecome difficult. To simplify them, assume that the cubic term is small, so its exponential can be expanded in a Taylor series (leaving the quadratic term in the exponent). Keeping only the smallest temperature-dependent term, show that in this limit x differs from zo by a term proportional to kT. Express the coefficient of this term in terms of the coefficients of the Taylor series foru(x)

(d) The interaction of noble gas atoms can be modeled using the Lennard Jones potential,

u(x)=u0x0x12-2x0x6

Sketch this function, and show that the minimum of the potential well is at x=x0, with depth u0. For argon, x0=3.9Aand u0=0.010eV. Expand the Lennard-Jones potential in a Taylor series about the equilibrium point, and use the result of part ( c) to predict the linear thermal expansion coefficient of a noble gas crystal in terms of u0. Evaluate the result numerically for argon, and compare to the measured value

α=0.0007K-1(at80K)

Short Answer

Expert verified

For argon factor will be doubled.

Step by step solution

01

part(a) Step 1:Given information

Let the particle be associated with position

02

part(a) Step 2: Simplify

x¯=xxP(x)=xxe-βu(x)Z

03

part(b) Step 1:Given information

The linear tem in the expansion is zero

04

part(b) Step 2: Simplify

xe-βux0+ax-x02dx=e-βux0xe-βax-x02dx=e-βux0y+x0e-βay2dy

e-βux0+ax-x02dx=e-βux0e-βax-x02dx=e-βux0e-βay2dy,

05

part(c) Step 1:Given information

we use Boltzman factor

06

part(c) Step 2: Simplify

x¯=e-βux0y+x0e-βay21-βby3dye-βux0e-βay21-βby3dy=x0-βby4e-βay2dye-βay2dy

x¯=x0-βb3/4β2a2π/βaπ/βa=x0-34bβa2=x0-34ba2kT.

07

part(d) Step 1:Given information

Lennard-Jones is positive

08

part(d) Step 2: Simplify

d3udx3=u0(-12)(-13)(-14)x012x-15-2(-6)(-7)(-8)x06x-9

α=-34ba2kx0=-34-252u0x03x0236u02kx0=748ku0=1.26×10-5eV/Ku0.

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Most popular questions from this chapter

Imagine a particle that can be in only three states, with energies -0.05 eV, 0, and 0.05 eV. This particle is in equilibrium with a reservoir at 300 K.

(a) Calculate the partition function for this particle.

(b) Calculate the probability for this particle to be in each of the three states.

(c) Because the zero point for measuring energies is arbitrary, we could just as well say that the energies of the three states are 0, +0.05 eV, and +0.10 eV, respectively. Repeat parts (a) and (b) using these numbers. Explain what changes and what doesn't.

In this problem you will investigate the behavior of ordinary hydrogen, H2, at low temperatures. The constant εis0.0076eV. As noted in the text, only half of the terms in the rotational partition function, equation6.3, contribute for any given molecule. More precisely, the set of allowed jvalues is determined by the spin configuration of the two atomic nuclei. There are four independent spin configurations, classified as a single "singlet" state and three "triplet" states. The time required for a molecule to convert between the singlet and triplet configurations is ordinarily quite long, so the properties of the two types of molecules can be studied independently. The singlet molecules are known as parahydrogen while the triplet molecules are known as orthohydrogen.

(a) For parahydrogen, only the rotational states with even values of j are allowed.Use a computer (as in Problem6.28) to calculate the rotational partition function, average energy, and heat capacity of a parahydrogen molecule. Plot the heat capacity as a function of kT/t

(b) For orthohydrogen, only the rotational states with odd values of jare allowed. Repeat part (a) for orthohydrogen.

(c) At high temperature, where the number of accessible even-j states is essentially the same as the number of accessible odd-j states, a sample of hydrogen gas will ordinarily consist of a mixture of 1/4parahydrogen and 3/4orthohydrogen. A mixture with these proportions is called normal hydrogen. Suppose that normal hydrogen is cooled to low temperature without allowing the spin configurations of the molecules to change. Plot the rotational heat capacity of this mixture as a function of temperature. At what temperature does the rotational heat capacity fall to half its hightemperature value (i.e., to k/2per molecule)?

(d) Suppose now that some hydrogen is cooled in the presence of a catalyst that allows the nuclear spins to frequently change alignment. In this case all terms in the original partition function are allowed, but the odd-j terms should be counted three times each because of the nuclear spin degeneracy. Calculate the rotational partition function, average energy, and heat capacity of this system, and plot the heat capacity as a function of kT/t.

(e) A deuterium molecule, D2, has nine independent nuclear spin configurations, of which six are "symmetric" and three are "antisymmetric." The rule for nomenclature is that the variety with more independent states gets called "ortho-," while the other gets called "para-." For orthodeuterium only even-j rotational states are allowed, while for paradeuterium only oddj states are allowed. Suppose, then, that a sample of D2gas, consisting of a normal equilibrium mixture of 2/3ortho and 1/3para, is cooled without allowing the nuclear spin configurations to change. Calculate and plot the rotational heat capacity of this system as a function of temperature.*

Fill in the steps between equations 6.51 and 6.52, to determine the average speed of the molecules in an ideal gas.

For a diatomic gas near room temperature, the internal partition function is simply the rotational partition function computed in section 6.2, multiplied by the degeneracy Zeof the electronic ground state.

(a) Show that the entropy in this case is

S=NkInVZeZrotNvQ+72.

Calculate the entropy of a mole of oxygen at room temperature and atmospheric pressure, and compare to the measured value in the table at the back of this book.

(b) Calculate the chemical potential of oxygen in earth's atmosphere near sea level, at room temperature. Express the answer in electron-volts

Each of the hydrogen atom states shown in Figure 6.2 is actually twofold degenerate, because the electron can be in two independent spin states, both with essentially the same energy. Repeat the calculation given in the text for the relative probability of being in a first excited state, taking spin degeneracy into account. Show that the results are unaffected.

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