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Statistical Mechanics - Physics at Oregon State University

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216 CHAPTER 9. GENERAL METHODS: CRITICAL EXPONENTS.<br />

which gives up to second order<br />

<br />

j(j − 1)<br />

1 + +<br />

4<br />

(N − j)(N − j − 1)<br />

−<br />

4<br />

or<br />

or<br />

<br />

N(N − 1)<br />

x<br />

4<br />

2<br />

1 + 1<br />

(j(j − 1) − jN − N(j + 1) + j(j + 1) + N) x2<br />

4<br />

1 + 1 2 2<br />

2j − 2jN x<br />

4<br />

We now have for the correl<strong>at</strong>ion length<br />

and after approxim<strong>at</strong>ing the logarithm<br />

<br />

ξ ≈ −j log 1 + 1<br />

−1 j(j − N)x2<br />

2<br />

ξ ≈<br />

2<br />

(N − j)x 2<br />

But now we are able to approxim<strong>at</strong>e the value of x by −2e −2βJ and obtain<br />

ξ ≈ e4βJ<br />

2(N − j)<br />

(9.132)<br />

(9.133)<br />

(9.134)<br />

(9.135)<br />

(9.136)<br />

(9.137)<br />

This is a different result, indeed. In the limit of zero temper<strong>at</strong>ure the hyperbolic<br />

tangent is very close to one, and all terms in the pair correl<strong>at</strong>ion function play<br />

a role. But the divergence is still exponential in stead of a power law, so th<strong>at</strong><br />

qualit<strong>at</strong>ive conclusion did not change. This is another consequence of the fact<br />

th<strong>at</strong> <strong>at</strong> zero temper<strong>at</strong>ure there is not really a phase transition.<br />

The previous results have some interesting consequences. First, suppose<br />

th<strong>at</strong> the correl<strong>at</strong>ion length is equal to the length of the chain. The whole chain<br />

will act in a correl<strong>at</strong>ed fashion. At a given time it is very likely th<strong>at</strong> all the<br />

spins point in the same direction and one would be tempted to call the chain<br />

magnetic. There will be times, however, where part of the chain is magnetized in<br />

one direction, and part in the other. Such a disturbance has a higher energy and<br />

will disappear. Nevertheless, this disturbance might switch the magnetiz<strong>at</strong>ion of<br />

the whole chain. An average over an infinite time therefore gives a non-magnetic<br />

st<strong>at</strong>e! If we make the chain longer, we have to go to a lower temper<strong>at</strong>ure for the<br />

correl<strong>at</strong>ion length to be equal to the chain-length. Fluctu<strong>at</strong>ions become more<br />

unlikely, and it will take longer for the chain to switch its magnetiz<strong>at</strong>ion. From<br />

a fundamental point of view, the chain is still non-magnetic. From a practical<br />

point of view, the chain is magnetic in a meta-stable st<strong>at</strong>e. Therefore, we could<br />

define a transition temper<strong>at</strong>ure T ∗ by ξ(T ∗ ) = N. But phase transitions are<br />

only defined in the thermodynamic limit, and we have limN→∞ T ∗ = 0. But it<br />

does tell us when finite size effects play a role. For a given N we can find T ∗

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