In Problem 7.28you found the density of states and the chemical potential for a two-dimensional Fermi gas. Calculate the heat capacity of this gas in the limit role="math" localid="1650099524353" kTεF· Also show that the heat capacity has the expected behavior when kTεF. Sketch the heat capacity as a function of temperature.

Short Answer

Expert verified

The heat capacity of the gas in the limit is CV=N(kπ)2T3εF.

The graph of heat capacity as a function of temperature is

Step by step solution

01

Given information

We have been given that the density of states and the chemical potential for a two-dimensional Fermi gas which we have found earlier in Problem 7.28isg(ε)=NεF.

We need to find the heat capacity of this gas in the limit kTεFand show that the heat capacity has the expected behavior when kTεF. Also we need to sketch the heat capacity as a function of temperature.

02

Simplify

The total energy is given by the following integral:

U=0εg(ε)n¯FD(ε)dε (Let this equation be (localid="1650103209259" 1))

We have found the energy density earlier in Problem 7.28such as

localid="1650102270353" g(ε)=NεF

Substitute the value of g(ε)in equation (localid="1650103517684" 1), we get:

U=NεF0εn¯FD(ε)dε

Integrating by parts, we get:

U=NεFε22n¯FD|0-NεF0ε22n¯FDεdε (Let this equation be (2))

If we substitute ε=0, the integral will become zero due to the dependence of the term on ε2and the first term vanishes.

The equation (2) reduces to :

U=-NεF0ε22n¯FDεdε (Let this equation be (3))

We know that n¯FD=1e(e-μ)kT+1

Taking derivative with respect to ε, we get:

localid="1650103912932" n¯FDε=1e(ε-μ)kT+1ε

n¯FDε=-1kTe(ε-μ)kT(e(ε-μ)kT+1)2

Let (ε-μ)kT=x, then we can write as:

dx=dεkT

We also need to change the boundaries of integration, so:

ε x

ε0 x-μkT

As kTμ, we can put -as the lower limit of integration.

The integral in equation (3) will become:

U=N2εF-ε2ex(ex+1)2dx (Let this equation be (localid="1650114310341" 4))

03

finding the values of integrals

Now expanding ε2about μusing Taylor series, we get:

ε2=μ2+2μ(ε-μ)x+(ε-μ)x2ε2=μ2+2μ(kTx)+(kTx)2

By substituting the value of in equation (4), we get three integrals say I1,I2,I3

The equation (4) will become:

U=N2εF[I1+I2+I3] (Let this equation be (5))

where,

I1=μ2-ex(ex+1)2dxI2=2kTμ-xex(ex+1)2dxI3=(kT)2-x2ex(ex+1)2dx

Simplifying the integrals I1,I2,I3, we get:

I1=μ2

The second integral is odd integral and the limits of integration are from to , so this integral is simply zero.

I2=0

I3=(kT)2π23=(kTπ)23

Substitute the values of in equation (5), we get:

U=N2εFμ2+(kTπ)23

Let μ=εF, we get:

U=N2εFεF2+(kTπ)23U=NεF2+N(kTπ)26εF

The heat capacity is the partial derivative of with respect to the temperature, that is:

CV=UTCV=NεF2+N(kTπ)26εFTCV=N(kπ)2T3εF

04

Graph

The graph of the heat capacity as a function of temperature is linear, where the slope of the line is Slope=N(kπ)23εF.

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Most popular questions from this chapter

When the attractive forces of the ions in a crystal are taken into account, the allowed electron energies are no longer given by the simple formula 7.36; instead, the allowed energies are grouped into bands, separated by gaps where there are no allowed energies. In a conductor the Fermi energy lies within one of the bands; in this section we have treated the electrons in this band as "free" particles confined to a fixed volume. In an insulator, on the other hand, the Fermi energy lies within a gap, so that at T = 0 the band below the gap is completely occupied while the band above the gap is unoccupied. Because there are no empty states close in energy to those that are occupied, the electrons are "stuck in place" and the material does not conduct electricity. A semiconductor is an insulator in which the gap is narrow enough for a few electrons to jump across it at room temperature. Figure 7 .17 shows the density of states in the vicinity of the Fermi energy for an idealized semiconductor, and defines some terminology and notation to be used in this problem.

(a) As a first approximation, let us model the density of states near the bottom of the conduction band using the same function as for a free Fermi gas, with an appropriate zero-point: g(ϵ)=g0ϵ-ϵc, where go is the same constant as in equation 7.51. Let us also model the density of states near the top

Figure 7.17. The periodic potential of a crystal lattice results in a densityof-states function consisting of "bands" (with many states) and "gaps" (with no states). For an insulator or a semiconductor, the Fermi energy lies in the middle of a gap so that at T = 0, the "valence band" is completely full while the-"conduction band" is completely empty. of the valence band as a mirror image of this function. Explain why, in this approximation, the chemical potential must always lie precisely in the middle of the gap, regardless of temperature.

(b) Normally the width of the gap is much greater than kT. Working in this limit, derive an expression for the number of conduction electrons per unit volume, in terms of the temperature and the width of the gap.

(c) For silicon near room temperature, the gap between the valence and conduction bands is approximately 1.11 eV. Roughly how many conduction electrons are there in a cubic centimeter of silicon at room temperature? How does this compare to the number of conduction electrons in a similar amount of copper?

( d) Explain why a semiconductor conducts electricity much better at higher temperatures. Back up your explanation with some numbers. (Ordinary conductors like copper, on the other hand, conduct better at low temperatures.) (e) Very roughly, how wide would the gap between the valence and conduction bands have to be in order to consider a material an insulator rather than a semiconductor?

Evaluate the integrand in equation 7.112as a power series in x, keeping terms through x4• Then carry out the integral to find a more accurate expression for the energy in the high-temperature limit. Differentiate this expression to obtain the heat capacity, and use the result to estimate the percent deviation of Cvfrom3NkatT=TDandT=2TD.

Starting from equation 7.83, derive a formula for the density of states of a photon gas (or any other gas of ultra relativistic particles having two polarisation states). Sketch this function.

The argument given above for why CvTdoes not depend on the details of the energy levels available to the fermions, so it should also apply to the model considered in Problem 7.16: a gas of fermions trapped in such a way that the energy levels are evenly spaced and non-degenerate.

(a) Show that, in this model, the number of possible system states for a given value of q is equal to the number of distinct ways of writing q as a sum of positive integers. (For example, there are three system states for q = 3, corresponding to the sums 3, 2 + 1, and 1 + 1 + 1. Note that 2 + 1 and 1 + 2 are not counted separately.) This combinatorial function is called the number of unrestricted partitions of q, denoted p(q). For example, p(3) = 3.

(b) By enumerating the partitions explicitly, compute p(7) and p(8).

(c) Make a table of p(q) for values of q up to 100, by either looking up the values in a mathematical reference book, or using a software package that can compute them, or writing your own program to compute them. From this table, compute the entropy, temperature, and heat capacity of this system, using the same methods as in Section 3.3. Plot the heat capacity as a function of temperature, and note that it is approximately linear.

(d) Ramanujan and Hardy (two famous mathematicians) have shown that when q is large, the number of unrestricted partitions of q is given approximately by

p(q)eπ2q343q

Check the accuracy of this formula for q = 10 and for q = 100. Working in this approximation, calculate the entropy, temperature, and heat capacity of this system. Express the heat. capacity as a series in decreasing powers of kT/η, assuming that this ratio is large and keeping the two largest terms. Compare to the numerical results you obtained in part (c). Why is the heat capacity of this system independent of N, unlike that of the three dimensional box of fermions discussed in the text?

Starting from the formula for CV derived in Problem 7.70(b), calculate the entropy, Helmholtz free energy, and pressure of a Bose gas for T<Tc. Notice that the pressure is independent of volume; how can this be the case?

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