scaling
scaling
Previously, we found that singular behaviour in the vicinity of a second order critical
point was characterised by a set of critical exponents {α, β, γ, δ, · · ·}. These power law
dependencies of thermodynamic quantities are a symptom of scaling behaviour. Mean-
field estimates of the critical exponents were found to be unreliable due to fluctuations.
However, since the various thermodynamic quantities are related, these exponents can not
be completely independent of each other. The aim of this chapter is to employ scaling
ideas to uncover relationships between them.
3.1 Homogeneity
The non-analytic structure of the Ginzburg-Landau model was found to be a coexistence
line for t < 0 and h = 0 that terminates at the critical point h = t = 0. Thermodynamic
quantities Q(t, h) in the vicinity of the critical point are characterised by various expo-
nents. In particular, within the saddle-point approximation we found that the free energy
density was given by
! " # 2
βF t 2 4 −t /u, h = 0, t < 0,
f≡ = minm m + um − h · m ∼ 4/3 1/2 (3.1)
V 2 −h /u h $= 0, t = 0.
In fact, the free energy can be described by a single homogeneous function1 in t and h
where ∆ is known as the “Gap exponent”. Comparison with Eq. (3.1) shows that, if we
set ∆ = 3/2, the correct asymptotic behaviour of f is obtained,
1 t2
lim gf (x) ∼ − , f (t, h = 0) ∼ − ,
x→0 u u
4/3
$ %4/3
x 2 h
lim gf (x) ∼ , f (t = 0, h) ∼ t ∼ h4/3 .
x→∞ u1/3 t∆
1
A function f (x) is said to be homogeneous of degree k if it satisfies the relation f (x) = bk f (bx).
where the actual exponents α and ∆ depend on the critical point being considered.
Heat Capacity: For example, the dependence on t is chosen to reproduce the heat
capacity singularity at h = 0. The singular part of the energy is obtained from
∂f
Esing. ∼ ∼ (2 − α)t1−α gf (h/t∆ ) − ∆ht1−α−∆ gf$ (h/t∆ ) ≡ t1−α gE (h/t∆ ),
∂t
where the prime denotes the derivative of the function with respect to the argument. Thus,
the derivative of one homogeneous function is another. Similarly, the second derivative
takes the form
∂2f
Csing. ∼ − ∼ t−α gC (h/t∆ ),
∂t2
reproducing the scaling Csing. ∼ t−α as h → 0.2
Magnetisation: Similarly the magnetisation is obtained from Eq. (3.3) using the
expression
∂f
m(t, h) ∼ ∼ t2−α−∆ gm (h/t∆ ).
∂h
In the limit x → 0, gm (x) is a constant, and m(t, h = 0) ∼ t2−α−∆ (i.e. β = 2 − α − ∆).
On the other hand, if x → ∞, gm (x) ∼ xp , and m(t = 0, h) ∼ t2−α−∆ (h/t∆ )p . Since this
limit is independent of t, we must have p∆ = 2 − α − ∆. Hence m(t = 0, h) ∼ h(2−α−∆)/∆
(i.e. δ = ∆/(2 − α − ∆) = ∆/β).
Susceptibility: Finally, calculating the susceptibility we obtain
∂m
χ(t, h) ∼ ∼ t2−α−2∆ gχ (h/t∆ ) ⇒ χ(t, h = 0) ∼ t2−α−2∆ ⇒ γ = 2∆ − 2 + α.
∂h
Thus the consequences of homogeneity are:
• The singular parts of all critical quantities, Q(t, h) are homogeneous, with the same
exponents above and below the transition.
• Because of the interconnections via thermodynamic derivatives, the same gap expo-
nent, ∆ occurs for all such quantities.
• All critical exponents can be obtained from only two independent ones, e.g. α, ∆.
2
It may appear that we have the freedom to postulate a more general form, C± = t−α± g± (h/t∆ ±)
with different functions for t > 0 and t < 0 that match at t = 0. However, this can be ruled out by the
condition that the free energy is analytic everywhere except on the coexistence line h = 0 and t < 0.
α + 2β + γ = 2 (Rushbrooke$ s Identity)
These identities can be checked against the following table of critical exponents. The first
three rows are based on a number of theoretical estimates in d = 3; the last row comes
from an exact solution in d = 2. The exponent identities are approximately consistent
with these values, as well as with all reliable experimental data.
α β γ δ ν η
d=3 n=1 Ising 0.12 0.31 1.25 5 0.64 0.05
n=2 XY-spin 0.00 0.33 1.33 5 0.66 0.00
n=3 Heisenberg −0.14 0.35 1.4 5 0.7 0.04
d=2 n=1 Ising 0 1/8 7/4 15 1 1/4
2. Close to criticality, the correlation length ξ is the most important length scale, and
is solely responsible for singular contributions to thermodynamic quantities.
The second condition determines the singular part of the free energy. Since ln Z(t, h)
is dimensionless and extensive (i.e. scales in proportion with the volume Ld ), it must take
the form
$ %d $ %d
L L
ln Z = × gs + × ga ,
ξ a
Spins correlated
in each box
L ξ
2 − α = dν (Josephson$ s Idenitity)
Identities obtained from the generalised homogeneity assumption involve the space
dimension d, and are known as hyperscaling relations. The relation between α and ν
is consistent with the exponents in the table above. However, it does not agree with the
mean-field values, α = 0 and ν = 1/2, which are valid for d > 4. Any theory of critical
behaviour must therefore account for the validity of this relation in low dimensions, and
its breakdown in d > 4.
Therefore, two independent exponents are sufficient to describe all singular critical be-
haviour.
An important consequence of these scaling ideas is that the critical system has an
additional dilation symmetry. Under a change of scale, the critical correlation functions
behave as
3
One notable exception is in d = 2, where dilation symmetry implies conformal symmetry.