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A new approach to producing volume periodic polymer-metal nanoparticle structures is presented. Periodic distribution of Ag nanoparticles in a polymer film can be obtained by applying the holographic patterning in the UV or visible spectral range to the composite material comprising photocurable monomers, photoinitiators and a solution of silver nitrate in acetonitrile. Photopolymerization of the composite in the interference pattern provides formation of a highly efficient volume grating composed of periodic polymer regions and Ag precursor-containing regions. Subsequent homogeneous UV irradiation and/or thermo-treatment of the grating causes reduction of silver ions to Ag nanoparticles in the areas of the film containing the metal precursor. Spectroscopic measurements confirm the formation of the nanoparticles in the gratings. Transmission electron microscopy showed a regular spatial distribution of well-defined Ag nanoparticles in a polymer film with a periodicity governed by the geometry of holographic structuring. The average diameter of nanoparticles can be controlled by the wavelength and intensity of holographic exposure as well as the composite formulation. A possible mechanism of silver nanoparticle formation by free radicals as reducing agents is presented.

Amplified spontaneous emission (ASE) is demonstrated in volume-distributed feedback (DFB) structures, formed by colloidal CdSe/ZnS nanocrystals and ZrO2 nanoparticles (NPs) in a polymer matrix. Periodic redistribution of the NPs in an organic matrix was carried out by holographic photopolymerization in a specially developed light-sensitive nanocomposite. The composite consists of two acrylate monomers and two types of inorganic NPs. The NPs provide for the formation of two co-phased gratings-a refractive index grating and an optical gain (losses) grating. The core-shell CdSe/ZnS nanocrystals are used as a gain medium, while ZrO2 NPs create the refractive index grating and enhance the distributed feedback. The period of the volume structure provides the feedback for lasing at the wavelength lambda(las) of about 575 nm in the second diffraction order. In contrast to known laser systems based on volume DFB cavities, in which the different components of the formulation provide optical gain and feedback, in our case the inorganic NPs serve as an emitting material and can provide simultaneously for feedback. By pumping of DFB structures by a titanium-sapphire laser (lambda(pump) = 400 nm, pulse duration of 120 fs) normal to the sample plane, the appearance of a sharp stimulated emission along the grating-vector direction is observed. Output intensity of ASE as a function of the pump energy shows a threshold behavior and full width at half-maximum (FWHM) of the ASE spectral band decreases from 33 to 12 nm.

We present a multigram scale, one-step nonaqueous synthesis route to monodisperse, highly crystalline ZrO(2) nanoparticles. The nanoparticles can be stabilized in nonpolar solvents via a simple functionalization procedure using only minute amounts of organic stabilizers. Their great potential in materials applications is demonstrated by the fabrication of organic-inorganic nanocomposites that can be selectively photopolymerized to inscribe extremely effective and volume holographic gratings with the highest refractive index contrast (n(1) of up to 0.024) achieved so far.