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Statistical Mechanics - Physics at Oregon State University

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8.4. DENSITY-MATRIX APPROACH (BRAGG-WILLIAMS APPROXIMATION.173<br />

A = log(B). We first look <strong>at</strong> the logarithm of Rn, Tn = log(Rn). The oper<strong>at</strong>ors<br />

Rn have a simple form, they are Hermitian, and the eigenvectors are simple.<br />

The only st<strong>at</strong>es th<strong>at</strong> can be mixed are st<strong>at</strong>es with different values of σn. But<br />

vectors th<strong>at</strong> have different values of σi with i = n are not mixed, and all eigenvectors<br />

of Rn have values for σi either +1 or −1. Since the eigenvectors of Tn<br />

are identical to the eigenvectors of Rn, the same is true for Tn. This implies<br />

th<strong>at</strong> we can write<br />

< σ1, · · · , σN|Tn|σ ′ 1, · · · , σ ′ N >= δσ1,σ ′ 1 δσ2,σ ′ 2 · · · τ(σn, σn) · · · (8.75)<br />

The only part of the space th<strong>at</strong> is mixed corresponds to σn, but since the<br />

eigenvectors of both oper<strong>at</strong>ors are teh same, we need to have<br />

τ = log(ρ) (8.76)<br />

Finally, because [Ri, Rj] = 0 we have log(RiRj) = log(Ri) log(Rj). This<br />

gives us th<strong>at</strong> log(ρ) = <br />

i log(Ti). Hence<br />

and<br />

< σ1, · · · , σN| log(ρ)|σ ′ 1, · · · , σ ′ N >=<br />

Tr ρ log(ρ) =<br />

N<br />

n=1<br />

N <br />

< σ1|ρ|σ1 > <br />

< σ2|ρ|σ2 > · · · <br />

n=1<br />

σ1<br />

σ2<br />

δσ1,σ ′ 1 δσ2,σ ′ 2 · · · 〈log(ρ)〉 (σn, σn) · · ·<br />

σn,σ ′ n<br />

(8.77)<br />

< σn|ρ|σ ′ n >< σ ′ n| log(ρ)|σn > · · ·<br />

(8.78)<br />

The trace of the oper<strong>at</strong>ors is equal to one, so all those sums in the equ<strong>at</strong>ion are<br />

replaced by one. This leaves<br />

Tr ρ log(ρ) =<br />

and we have<br />

N<br />

<br />

n=1 σn,σ ′ n<br />

< σn|ρ|σ ′ n >< σ ′ n| log(ρ)|σn >= NTr ρ log(ρ) (8.79)<br />

S = −kBNTr ρ log(ρ) (8.80)<br />

as expected, since all sites are equivalent and contributions from different sites<br />

are not mixed. Nevertheless, it was important to follow the m<strong>at</strong>hem<strong>at</strong>ical deriv<strong>at</strong>ion<br />

to make sure th<strong>at</strong> our intuitive expect<strong>at</strong>ion was indeed correct.<br />

Next we need to minimize the free energy<br />

G(h, T ) min<br />

m,a<br />

<br />

− 1<br />

2 JNqm2 <br />

− hNm + NkBT Tr ρ log(ρ)<br />

(8.81)

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