At T = 0, equation 8.50 says that s¯=1. Work out the first temperature-dependent correction to this value, in the limit βn1. Compare to the low-temperature behaviour of a real ferromagnet, treated in Problem 7.64.

Short Answer

Expert verified

Therefore,

ϵF=40MeVTF=4.638×1011K

This is hotter than the centre of any ordinary star. We can treat the nucleus as a degenerate.

Step by step solution

01

Given information

At T = 0, equation 8.50 says thats¯=1 . Work out the first temperature-dependent correction to this value, in the limit βn1.

02

Explanation

We must change the Fermi energy since each spatial wave function may carry four nucleons, hence the first equation 7.38 must be multiplied by a factor of two, yielding:

N=2πnmax33

Solve for nmax:

nmax=3N2π1/3

Fermi energy in terms of nmax:

ϵF=h2nmax28mL2

Substitute with nmax:

ϵF=h28mL23N2π2/3ϵF=h28m3N2πL32/3ϵF=h28m3N2πV2/3

Where, V=L3

The number density of gas is:

NV=0.18fm-3=0.181fm3×fm31.0×10-153m3=1.8×1044m-3

Substitute with the values:

ϵF=6.626×10-34J·s281.67×10-27kg31.8×1044m-32π2/3=6.40×10-12JϵF=40MeV

03

Explanation

The Fermi energy is calculated by multiplying the Boltzmann constant by the Fermi temperature, which is:

ϵF=kTFTF=ϵFk

Substitute with fermi energy:

TF=6.40×10-12J1.38×10-23J/KTF=4.638×1011K

This is hotter than the centre of any ordinary star. We can treat the nucleus as a degenerate.

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Most popular questions from this chapter

Show that the Lennard-Jones potential reaches its minimum value at r=r0, and that its value at this minimum is -u0. At what value of rdoes the potential equal zero?

The Ising model can be used to simulate other systems besides ferromagnets; examples include anti ferromagnets, binary alloys, and even fluids. The Ising model of a fluid is called a lattice gas. We imagine that space is divided into a lattice of sites, each of which can be either occupied by a gas molecule or unoccupied. The system has no kinetic energy, and the only potential energy comes from interactions of molecules on adjacent sites. Specifically, there is a contribution of -u0to the energy for each pair of neighbouring sites that are both occupied.

(a) Write down a formula for the grand partition function for this system, as a function of u0, T, and p.

(b) Rearrange your formula to show that it is identical, up to a multiplicative factor that does not depend on the state of the system, to the ordinary partition function for an Ising ferromagnet in the presence of an external magnetic field B, provided that you make the replacements u04ϵand μ2μBB-8ϵ. (Note that is the chemical potential of the gas while uB is the magnetic moment of a dipole in the magnet.)

(c) Discuss the implications. Which states of the magnet correspond to low density states of the lattice gas? Which states of the magnet correspond to high-density states in which the gas has condensed into a liquid? What shape does this model predict for the liquid-gas phase boundary in the P-T plane?

Modify the ising program to compute the total magnetisation (that is, the sum of all the s values) for each iteration, and to tally how often each possible magnetisation value occurs during a run, plotting the results as a histogram. Run the program for a 5 x 5 lattice at a variety of temperatures, and discuss the results. Sketch a graph of the most likely magnetisation value as a function of temperature. If your computer is fast enough, repeat for a 10 x 10 lattice.

To quantify the clustering of alignments within an Ising magnet, we define a quantity called the correlation function, c(r). Take any two dipoles i and j, separated by a distance r, and compute the product of their states: sisj. This product is 1 if the dipoles are parallel and -1 if the dipoles are antiparallel. Now average this quantity over all pairs that are separated by a fixed distance r, to |obtain a measure of the tendency of dipoles to be "correlated" over this distance. Finally, to remove the effect of any overall magnetisation of the system, subtract off the square of the average s. Written as an equation, then, the correlation function is

c(r)=sisj¯-si¯2

where it is understood that the first term averages over all pairs at the fixed distance r. Technically, the averages should also be taken over all possible states of the system, but don't do this yet.

(a) Add a routine to the ising program to compute the correlation function for the current state of the lattice, averaging over all pairs separated either vertically or horizontally (but not diagonally) by r units of distance, where r varies from 1 to half the lattice size. Have the program execute this routine periodically and plot the results as a bar graph.

(b) Run this program at a variety of temperatures, above, below, and near the critical point. Use a lattice size of at least 20, preferably larger (especially near the critical point). Describe the behaviour of the correlation function at each temperature.

(c) Now add code to compute the average correlation function over the duration of a run. (However, it's best to let the system "equilibrate" to a typical state before you begin accumulating averages.) The correlation length is defined as the distance over which the correlation function decreases by a factor of e. Estimate the correlation length at each temperature, and plot graph of the correlation length vs.

Starting from the partition function, calculate the average energy of the one-dimensional Ising model, to verify equation 8.44. Sketch the average energy as a function of temperature.

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