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Effective volume holographic structures based on organic-inorganic photopolymer nanocomposites
(2009)
We demonstrate a practical approach for the development of a broad range of nanocomposites based on acrylate polymers and organically capped inorganic nanoparticles (NPs). The submicrometer scale volume patterning of the nanocomposites using holographic photopolymerization was investigated. The specific adjustment of both the material parameters (core-shell of the NP, monomer mixture, concentrations) and the patterning conditions led to materials that were suitable for the fabrication of effective optical diffractive elements and specific functional microdevices with light-emissive and nonlinear optical (NLO) properties. The nanocomposite preparation and properties, their holographic performance and some examples of functional polymer-NP structures are reported.
The influence of molecular architecture on light-induced SRG formation was investigated. Polymers with different degree of branching were synthesized by ATRP and functionalized with azobenzene chromophores. The polymers differ only in their architecture - linear, 4-, 6-, or 12-arms stars. The photo-induced dichroism as well as the efficiency of SRG formation was similar for all polymers of this series. New consideration for the origin of the driving force was used to explain this behavior. The comparable SRG inscription rate in differently branched polymers can be rationalized by assuming that azobenzene acts as an internal molecular motor and can cause a non-turbulent motion on a scale smaller than that on which normal entanglement restriction forces act.