Recent research on an acrylamide-based photopolymerizable holographic recording material is presented. The recording characteristics of the material are discussed in detail in terms of sensitivity, diffraction efficiency, recording linearity, resolution limit, and sources of noise. Although the resolution is not sufficient for reflection holography, the recording characteristics are excellent for transmission gratings. The material was found to suffer no shrinkage during recording, and high-diffraction-efficiency slanted gratings were made. Finally, the suitability of this self-developing material to both double-exposure and real-time holographic interferometry is demonstrated.

A reflection hologram for visual indication of environmental humidity has been studied. The hologram is recorded in a self-developing photopolymer and changes color when exposed to a change in humidity and is fully reversible. The range of color change, reversibility, and the response time of the hologram have been studied in a controlled humidity environment. Fully reversible holograms with response times from few seconds to tens of minutes have been designed. Extremely sensitive bright visual humidity indicators, capable of dramatic color change within a few seconds of breathing on them are demonstrated.

Novel nanocomposites consisting of a water-soluble acrylamide-based photopolymer and colloidal zeolite nanoparticles of zeolite Beta and zeolite A were prepared. The interactions between the photopolymer components and zeolite nanoparticles in the photopolymerizable nanocomposites were characterized for the first time by ${}^{13}\mathrm{C}$ nuclear magnetic resonance and visible spectroscopy. It was found that the zeolite Beta nanoparticles (up to $5\text{wt. \%}$) behave as a noninert additive, resulting in an effective increase in layer thickness, which causes doubling of the diffraction efficiency of the nanocomposite in comparison to that of the undoped photopolymer. On the other hand, the nanocomposite containing zeolite A nanoparticles showed no evidence of interaction with the polymer matrix, had similar values of diffraction efficiency, and—up to a small addition of nanoparticles (up to $2.5\text{wt. \%}$)—showed slightly higher light-induced refractive index modulation of the grating when compared to the undoped photopolymer. The good optical compatibility between the zeolite nanoparticles and the polymer allows a versatile design of photopolymerizable nanocomposites with different properties by selecting the adequate type of zeolite. The nanocomposite containing zeolite Beta nanoparticles demonstrates selective sensing be havior toward toluene and can be coated in either glass or plastic substrates and exposed directly to the environmental conditions.

Results from the investigation of the diffusion processes in a dry acrylamide-based photopolymer system are presented. The investigation is carried out in the context of experimental research on optimization of the high-spatial-frequency response of the photopolymer. Tracing the transmission holographic grating dynamics at short times of exposure is utilized to measure diffusion coefficients. The results reveal that two different diffusion processes contribute with opposite sign to the refractive-index modulation responsible for the diffraction grating buildup. Monomer diffusion from dark to bright fringe areas increases the refractive-index modulation. It is characterized with diffusion constant D ₀ = 1.6 × 10^-7 cm²/s. A second diffusion process takes place during the recording. It decreases the refractive-index modulation and we ascribe it to diffusion of short-chain polymer molecules or radicals from bright to dark fringe areas. The estimated diffusion coefficient for this process is D ₀ = 6.35 × 10^-10 cm²/s. The presence of the second process could be responsible for the poor high-spatial-frequency response of the investigated photopolymer system. Comparison with the diffusion in photopolymer systems known for their good response at high spatial frequencies shows that both investigated diffusion processes occur in a much faster time scale.