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Statistical Mechanics - Physics at Oregon State University

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5.4. PROBLEMS FOR CHAPTER 5 115<br />

degener<strong>at</strong>e orbitals! Hence <strong>at</strong> T = 0 the number of particles in a ground st<strong>at</strong>e<br />

orbital (1, 1, 1, s) is N<br />

2S+1 and the total number of particles in all ground st<strong>at</strong>e<br />

orbitals (1, 1, 1, s) together is N. In other words, all particles are in the ground<br />

st<strong>at</strong>e orbital (1, 1, 1) defined without spin. In a number of books one changes<br />

the actual definition of the distribution function by<br />

fBE(ɛ) =<br />

2S + 1<br />

e ɛ−µ<br />

k B T − 1<br />

(5.141)<br />

and similar for fermions. Keep this in mind.<br />

The number of particles in the ground st<strong>at</strong>e orbital(s) has a sharp transition<br />

according to our formulas. This is because we took the thermodynamic limit.<br />

If we keep both terms in the expression for n, however, this transition is smooth<br />

for finite volumes. Even for values above the Einstein temper<strong>at</strong>ure there are<br />

some particles in the ground st<strong>at</strong>e orbital. For most experimental situ<strong>at</strong>ions,<br />

however, the differences are small and one is allowed to use the 3<br />

2<br />

power law<br />

formula. Only right <strong>at</strong> the transition does one see finite size effects. The process<br />

in which a macroscopic number of particles go into the ground st<strong>at</strong>e orbital<br />

is called Bose-Einstein condens<strong>at</strong>ion. It is observed experimentally in liquid<br />

Helium. Below 2.17 K liquid Helium has no viscosity and a very large thermal<br />

conductivity. One can think of these effects as a manifest<strong>at</strong>ion of a macroscopic<br />

quantum st<strong>at</strong>e. Since many particles are in the same orbital, there are no<br />

interference effects between their wave functions and they all act in a coherent<br />

way.<br />

Note, however, th<strong>at</strong> our calcul<strong>at</strong>ions are performed for a gas. In a real<br />

experiment the temper<strong>at</strong>ure is very low and the m<strong>at</strong>erial is a liquid. Corrections<br />

due to particle interactions are needed and the actual calcul<strong>at</strong>ions are much more<br />

difficult. Also, our calcul<strong>at</strong>ions only show th<strong>at</strong> there is a transition. In order<br />

to describe the st<strong>at</strong>e with Bose-Einstein condens<strong>at</strong>ion we need to take particle<br />

interactions into account! Again, these correl<strong>at</strong>ion effects are very difficult to<br />

incorpor<strong>at</strong>e.<br />

5.4 Problems for chapter 5<br />

Problem 1.<br />

An ideal gas consists of H2 molecules. We need six degrees of freedom to<br />

describe such a molecule. Three pertain to the motion of the center of mass<br />

of the molecule and these degrees of freedom follow the st<strong>at</strong>istical mechanical<br />

description of an ideal gas. There are three internal degrees of freedom, two<br />

pertaining to rot<strong>at</strong>ions and one to vibr<strong>at</strong>ions of each molecule. The values for<br />

the energy levels of the rot<strong>at</strong>ional degrees of freedom are kBTrj(j + 1) and for<br />

the vibr<strong>at</strong>ional st<strong>at</strong>es kBTv(n + 1<br />

2 ). Quantum effects start to play a role below<br />

a temper<strong>at</strong>ure Tq, defined by nQ(Tq) = n. The H2 gas in enclosed in a fixed

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