Numéro |
J. Phys. II France
Volume 5, Numéro 8, August 1995
|
|
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Page(s) | 1165 - 1191 | |
DOI | https://doi.org/10.1051/jp2:1995175 |
J. Phys. II France 5 (1995) 1165-1191
The Phenomenological Functions that Characterize the Surface Free Energy Density of Nematic Liquid Crystals: A Microscopic Analysis
S. Faetti1, 2 and M. Riccardi11 Dipartimento di Fisica dell'Universita' di Pisa, Piazza Torricelli 2, 56100 Pisa, Italy
2 Istituto Nazionale di Fisica della Materia, Piazza Torricelli 2, 56100 Pisa, Italy
(Received 10 February 1995, revised in final form 19 April 1995, accepted 21 April 1995)
Abstract
In a recent paper, Faetti proposed a new phenomenological expression for the surface free energy density
of a nematic liquid crystal in contact with an isotropic substrate.
depend on director n, on the unit vector k orthogonal to the interface and on their gradients at the interface. Five different terms appear in the expression of
. The first term is the standard anchoring energy contribution, the second and third terms are elastic contributions that
depend on the surface tangential director gradients, the fourth and fifth terms are new geometrical contributions that account
for the effect of a local curvature of the interfaces. The expression of the surface free energy density is characterized
by five phenomenological functions
and
A2(nk) where
nk is the scalar product n
k
. In this paper we give the first microscopic calculation of these new surface functions by using a simplified microscopic
model of intermolecular interactions. Surface functions
, and
K24*(nk) are found to be of the same order of magnitude of the Frank bulk elastic constants, whilst
K13*(nk)=0. The geometric surface functions
A1(nk) and
A2(nk) satisfy the simple relation
. Both the results
K13*(nk)=0 and
are shown to be a direct consequence of the invariance with respect to the transform
of the interaction energy between molecules.
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