Holographic gratings formed through the anisotropic phase separation of liq
uid crystals show promise as switchable optical elements. In order to form
useful elements, however, it is necessary to control the nanoscale morpholo
gies within the grating films. In this manuscript, we evaluate the role of
monomer functionality on the morphology and the electro-optical properties
of both gratings and conventional scattering polymer-dispersed liquid cryst
al (PDLC) films. Both of these structures are formed using polymerization-i
nduced phase separation (PIPS) of liquid crystals from a cross-linked polym
er formed through free-radical photo-polymerization. Floodlit (uniform illu
mination) films and holographic gratings (from non-uniform illumination cau
sed by the interference of two laser beams) were made using monomers with 2
-5 acrylate groups, while keeping the LC concentration constant in the syru
ps. The morphologies of these films were examined using low voltage scannin
g electron microscopy (LVSEM). In all cases, very small LC domains were for
med with little indication of growth or coalescence. Lowering monomer funct
ionality reduced the volume fraction of phase-separated domains in the floo
dlit samples. For the grating samples, the local volume fraction and the LC
domain sizes decreased substantially as the monomer functionality was decr
eased. Using detailed image analysis, differences in the anisotropy of the
domains was also probed. A much stronger tendency to form anisotropically-s
haped domains was observed for the higher functional syrups. These domain a
nisotropy differences are correlated with the number of reactive double bon
ds per monomer and are suggestive of local environmental differences exerte
d at the time of the domain formation. (C) 1999 Elsevier Science Ltd. All r
ights reserved.