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
6¼
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
(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”
Search WWH ::
Custom Search