Further Reading
[1] K. Binder (ed.), Monte-Carlo methods in statistical physics, Springer-Verlag
(New York, 1986).
[2] J.J. Binney, N.J. Dowrick, A.J. Fisher, and M.E. Newman, The Theory of
Critical Phenomena, Oxford University Press (Oxford, 1992).
[3] J. Cardy, Scaling and Renormalization in Statistical Physics, Cambridge University Press (Cambridge, 1996).
[4] W. Greiner, L. Neise, and H. Stocker, Thermodynamics and Statistical Mechanics, Springer-Verlag (New York, 1995).
[5] K. Huang, Statistical Mechanics, J. Wiley (New York, 1987).
[6] R. Kubo, Statistical Mechanics, North Holland (Amsterdam, 1967).
[7] L.D. Landau and E.M. Lifshitz, Statistical Physics I,II, Pergamon Press (Oxford, 1980).
[8] S.-k. Ma, Modern Theory of Critical Phenomena, Benjamin (Reading, 1976).
[9] B.M. McCoy and T.T. Wu, The Two-Dimensional Ising Model, Harvard (Cambridge, 1973).
[10] M. Plischke and B. Bergersen, Equilibrium Statistical Mechanics, World
Scientific (Singapore, 1994).
[11] F. Schwabl, Statistical Mechanics, Springer Verlag (Berlin, 2002).
[12] H.E. Stanley, Phase Transitions and Critical Phenomena, Oxford University
Press (London, 1971).
129
I. Vilfan
Statistical Mechanics
Chapter 4
[13] K.G. Wilson, Scientific American, 241, 140 (1979).
[14] Julia M Yeomans, Statistical Mechanics of Phase Transitions, Clarendon
(Oxford, 1992).
130
Appendix A
Distribution Functions
We have to distinguish three kinds of systems:
(a) identical but distinguishable particles (classical particles)
(b) identical indistinguishable particles with half-integer spin (Fermi-ons)
(c) identical indistinguishable particles with integer spins (Bosons)
The occupation probability of a state i with energy Ei is:
(a-Maxwell-Boltzmann):
1
(A.1)
n(Ei ) = Ei
e
2
Maxwell Boltzmann distrubution
n(E)
1: T = 1 000 K
2: T = 5 000 K
1
3: T = 10 000 K
3
2
1
0
0
0.5
1
Energy (eV)
(b-Fermi-Dirac):
n(Ei ) =
1.5
1
e(Ei F )
(c-Bose-Einstein):
n(Ei ) =
1
.
1
eEi
131
+1
(A.2)
(A.3)
I. Vilfan
Statistical Mechanics
Appendix A
2
Fermi Dirac distrubution
EF = 1 eV
1: T = 0 K
n(E)
2: T = 1 000 K
2: T = 5 000 K
1
3
3: T = 10 000 K
0
0
0.5
1
Energy (eV)
1.5
5
Bose Einstein distrubution
n(E)
1: T = 1 000 K
2: T = 5 000 K
3: T = 10 000 K
3
2
1
0
0
0.5
1
Energy (eV)
132
1.5
Appendix B
Maxwell Relations
Let df be a total differential of the function f (x, y). Then,
df = u(x, y)dx + v(x, y)dy
with
u(x, y) =
and
u
y
=
x
f
x
v(x, y) =
2f
yx
2f
xy
(B.1)
f
y
v
x
(B.2)
x
(B.3)
This is a very useful relation that - when applied to thermodynamic functions gives the Maxwell relations:
T
V
!
S
T
p
S
p
=
S
S
V
p
=
S
V
S
=
T
133
p
T
(B.4)
(B.5)
V
=
T
(B.6)
(B.7)
!
V
I. Vilfan
Statistical Mechanics
134
Appendix B
Appendix C
Basic Thermodynamic Relations of
Magnetic Systems Revisited
The internal energy is:
U (S, M ) =
Ji,j hSi Sj i
(C.1)
hiji
where S is the entropy, M is the total magnetic moment (in dimensionless units),
M = N m, m is the magnetic moment per lattice site, m = hSi i. Ji,j is the
exchange interaction between the spins i and j. The (magnetic) enthalpy is (here
we will use E for the enthalpy, to avoid confusion with the field H):
E(S, H) = U HM hHi
(C.2)
where H is the magnetic field in units of energy. The Helmholtz free energy is:
F (T, M ) = kB T ln Z(T, M, N ) = U T S
(C.3)
and its total differential is
dF = S dT + H dM
(C.4)
(see Table II of Part I; the number of spins N is constant): The Gibbs free energy
is
G(T, H) = kB T ln Y (T, H) = E T S
= F HM = U T S HM
135
(C.5)
I. Vilfan
Statistical Mechanics
Appendix C
and its differential is
dG = S dT M dH
(C.6)
Here, we introduced also the corresponding partition functions Z and Y . From
Eq. (C.4) we get immediately the equation of state:
F
M
H=
(C.7)
T,N
From Eq. (C.6) we also get an equation of state:
G
M =
H
!
T,N
E
=
H
(C.8)
S,N
Of course, the equations (C.7) and (C.8) must lead to the same equation, they are
just two ways of writing the equation of state. When we want to study systems at
constant H (and not at constant M ), the more convenient thermodynamic potential
is the Gibbs free energy G(T, H, N ) instead of the Helmholtz free energy.
Other useful thermodynamic relations are:
CH = T
S
T
CM = T
T =
S =
!
H
dU
=
= T
dT
S
T
M
H
M
H
= T
M
2G
T 2
2F
T 2
(C.9)
H
(C.10)
H
2G
=
H 2
2E
=
H 2
136
(C.11)
T
(C.12)
S