Chemistry Reference
In-Depth Information
Fig. 3 Evolution of the order
parameter for various fields
ranging from no field ( G ¼ 0)
to below-critical ( G < G C ),
and supercritical ( G > G C ).
The dotted lines denote the
discontinuity for the cases
G ¼ 0 and G < G C , the
dashed line stands for the
continuous evolution of the
order parameter at the critical
point ( G ¼ G C ) and T IN
denotes the transition
temperature of the case
without a field ( G ¼
0.6
G =0
0.4
G < G c
G > G c
0.2
G = G c
0)
0.0
-5
0
5
10
T - T IN (K)
;
1
2
3 cos 2
S ¼
y
1
(2)
where
denotes the angle between the molecular axis and the director n. In the
isotropic phase, the molecular orientations are random and
y
cos 2
h
yi¼
1/3, which
yields S ¼
0.
Externally applied fields that conjugate to the nematic order parameter can
induce some orientational order in the isotropic phase (which is called the parane-
matic order, in analogy with, e.g. paramagnetism) and suppress or even eliminate
the I-N discontinuity for strong field values. An additional linear term
0, while in the nematic phase S
GS must be
added to the free-energy expansion to account for the coupling between the applied
field G and the order parameter S :
1
2 aðT T ÞS 2
1
3 BS 3
1
4 CS 4
F ¼
þ
þ
GS:
(3)
Providing the field is smaller than its critical value:
G C ¼B 3
27 C 2
=
;
(4)
the discontinuity decreases but the phase transition remains first order (see Figs. 2
and 3 ). The discontinuity vanishes at G ¼ G C and the transition becomes continuous
(second order) at a single critical point. When G > G C , the transition is driven
beyond the critical point to the supercritical regime. The term “supercritical”
 
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