Sometimes it is useful to know the free energy of a photon gas.

(a) Calculate the (Helmholtz) free energy directly from the definition

(Express the answer in terms of T' and V.)

(b) Check the formula S=-(F/T)Vfor this system.

(c) Differentiate F with respect to V to obtain the pressure of a photon gas. Check that your result agrees with that of the previous problem.

(d) A more interesting way to calculate F is to apply the formula F=-kTlnZ separately to each mode (that is, each effective oscillator), then sum over all modes. Carry out this calculation, to obtain

F=8πV(kT)4(hc)30x2ln1-e-xdx

Integrate by parts, and check that your answer agrees with part (a).

Short Answer

Expert verified

Hence, the free energy is F=-13U

Step by step solution

01

Given information

Sometimes it is useful to know the free energy of a photon gas.

F= U-TS.

02

Explanation

The Helmholtz free energy is:

F=U-TS(1)

The total energy is:

U=8π5(kT)415(hc)3V

The entropy is:

S=32π545VkThc3k

Let,

A=8π2k415(hc)3

The total energy and entropy is:

U=AVT4andS=43AVT3

Substitute into (1)

F=AVT4-43AVT4F=-13AVT4F=-13U

03

Explanation

(b) At constant volume, the entropy equals the negative partial derivative of the Helmholtz energy with respect to temperature.

S=-FTV

Substitute F,

S=-T-13AVT4S=43AVT3

(c) At constant temperature, the pressure equals the negative partial derivative of the Helmholtz energy with respect to the volume, i.e.

P=-FVT

Substitute with F

P=-V-13AVT4P=13AT4P=13UV

(d)The Helmholtz free energy for one mode is given by:

F=-kTln(Z)

Where Z is partition function and is given as:

Z=11-e-ϵ/kT

Substitute in the above equation:

F=-kTln11-e-ϵ/kTF=kTln1-e-ϵ/kT

Because we have two polarisation modes, the total Helmholtz free energy equals the sum of F over all modes increased by a factor of two.

F=2nxnynzkTln1-e-ϵ/kT=2nx,ny,nzkTln1-e-ϵ/kT

04

Explanation

Consider we have a cubic box with volume of V and side width of L, the allowed energy for the photon is:

ϵ=hcn2L

Hence

F=2nx,ny,nzkTln1-e-hcn/2LkT

Now we need to convert the total to an integral in spherical coordinates, which we can do by multiplying it by the spherical integration factor n2sin(θ), which gives us:

role="math" localid="1647765663139" F=2kT0π/2dΦ0π/2sin(θ)dθ0n2ln1-e-hcn/2LkTdnF=πkT0n2ln1-e-hcn/2LkTdn

Let

x=hcn2LkTdx=hc2LkTdn

Thus,

F=πkT2LkThc30x2ln1-e-xdx

Volume of the box is:

F=8πkTVkThc30x2ln1-e-xdx

Integrate by parts:

F=8πkTVkThc3x33ln1-e-x0-0x33e-x1-e-x

Substituting values

F=-8πkTVkThc30x33e-x1-e-xF=-8π3V(kT)4(hc)30x3e-x1-e-xF=-8π3V(kT)4(hc)30x3ex-1

Comparing with the equation,

F=-13U

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Most popular questions from this chapter

Suppose you have a "box" in which each particle may occupy any of 10single-particle states. For simplicity, assume that each of these states has energy zero.

(a) What is the partition function of this system if the box contains only one particle?

(b) What is the partition function of this system if the box contains two distinguishable particles?

(c) What is the partition function if the box contains two identical bosons?

(d) What is the partition function if the box contains two identical fermions?

(e) What would be the partition function of this system according to equation 7.16?

(f) What is the probability of finding both particles in the same single particle state, for the three cases of distinguishable particles, identical bosom, and identical fermions?

In a real hemoglobin molecule, the tendency of oxygen to bind to a heme site increases as the other three heme sites become occupied. To model this effect in a simple way, imagine that a hemoglobin molecule has just two sites, either or both of which can be occupied. This system has four possible states (with only oxygen present). Take the energy of the unoccupied state to be zero, the energies of the two singly occupied states to be -0.55eV, and the energy of the doubly occupied state to be -1.3eV(so the change in energy upon binding the second oxygen is -0.75eV). As in the previous problem, calculate and plot the fraction of occupied sites as a function of the effective partial pressure of oxygen. Compare to the graph from the previous problem (for independent sites). Can you think of why this behavior is preferable for the function of hemoglobin?

Consider a two-dimensional solid, such as a stretched drumhead or a layer of mica or graphite. Find an expression (in terms of an integral) for the thermal energy of a square chunk of this material of area , and evaluate the result approximately for very low and very high temperatures. Also, find an expression for the heat capacity, and use a computer or a calculator to plot the heat capacity as a function of temperature. Assume that the material can only vibrate perpendicular to its own plane, i.e., that there is only one "polarization."

The heat capacity of liquid H4ebelow 0.6Kis proportional to T3, with the measured valueCV/Nk=(T/4.67K)3. This behavior suggests that the dominant excitations at low temperature are long-wavelength photons. The only important difference between photons in a liquid and photons in a solid is that a liquid cannot transmit transversely polarized waves-sound waves must be longitudinal. The speed of sound in liquid He4is 238m/s, and the density is 0.145g/cm3. From these numbers, calculate the photon contribution to the heat capacity ofHe4in the low-temperature limit, and compare to the measured value.

Show that when a system is in thermal and diffusive equilibrium with a reservoir, the average number of particles in the system is

N=kTZZμ

where the partial derivative is taken at fixed temperature and volume. Show also that the mean square number of particles is

N2¯=(kT)2Z2Zμ2

Use these results to show that the standard deviation of Nis

σN=kTN/μ,

in analogy with Problem6.18Finally, apply this formula to an ideal gas, to obtain a simple expression forσNin terms ofN¯Discuss your result briefly.

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