Photoanisotropic materials, in particular azodyes and azopolymers, have attracted significant research interest in the last decades. This is due to their applications in polarization holography and 4G optics, enabling polarization-selective diffractive optical elements with unique properties, including circular polarization beam-splitters, polarization-selective bifocal lenses, and many others. Numerous methods have been applied to increase the photoinduced birefringence of these materials, and as a result, to obtain polarization holographic elements with a high diffraction efficiency. Recently, a new approach has emerged that has been extensively studied by many research groups, namely doping azobenzene-containing materials with nanoparticles with various compositions, sizes, and morphologies. The resulting nanocomposites have shown significant enhancement in their photoanisotropic response, including increased photoinduced birefringence, leading to a higher diffraction efficiency and a larger surface relief modulation in the case of polarization holographic recordings. This review aims to cover the most important achievements in this new but fast-growing field of research and to present an extensive comparative analysis of the result, reported by many research groups during the last two decades. Different hypotheses to explain the mechanism of photoanisotropy enhancement in these nanocomposites are also discussed. Finally, we present our vision for the future development of this scientific field and outline its potential applications in advanced photonics technologies.

During polarization holographic recording in azopolymer thin films, usually together with the volume anisotropic grating, a surface relief grating (SRG) is also formed. By using two consecutive exposures, it is possible to obtain a two-dimensional (2D) grating. To the best of our knowledge, the polarization properties of such gratings have not been studied yet. To determine the influence of the surface relief on the polarization selectivity of the 2D gratings, we propose two methods to suppress the SRG formation: by varying the recording conditions or varying the sample structure. In these experiments we have used the commercially available azopolymer PAZO, poly[1-4-(3-carboxy-4-hydrophenylazo) benzene sulfonamido]-1,2-ethanediyl, sodium salt] to perform the polarization holographic recording using a 442 nm He-Cd laser. As indicated by our results, when the surface relief is present, it strongly dominates the response of the 2D grating and it behaves almost as a scalar polarization insensitive grating. Conversely, when the SRG formation is suppressed, the polarization properties of the 2D grating in all four diffracted orders are very well pronounced. In this way, we demonstrate that we can easily control SRG formation and, if desired, obtain 2D grating with high surface relief modulation, or alternatively record polarization-selective 2D gratings with virtually no surface relief.

In this work, we study the polarization properties of diffraction gratings recorded in thin films of the azopolymer PAZO (poly[1-[4-(3-carboxy-4-hydroxyphenylazo)benzene sulfonamido]-1,2-ethanediyl, sodium salt]) using digital polarization holography. Using two quarter-wave plates, the phase retardation of each pixel of the SLM is converted into the azimuth rotation of linearly polarized light. When recording from the azopolymer side of the sample, significant surface relief amplitude is observed with atomic force microscopy. In contrast, recording from the substrate side of the sample allows the reduction of the surface relief modulation and the obtaining of polarization gratings with characteristics close to an ideal grating, recorded with two orthogonal circular polarizations. This can be achieved even with a four-pixel period of grating, as demonstrated by our results.

We present a study of the birefringence photoinduced in thin nanocomposite films of an azopolymer (PAZO) doped with different concentrations of nanoparticles (NPs) of ZnO with spherical shape and size in the range 40 – 100 nm. The nanocomposite thin films were prepared by electrospray deposition of ZnO over a thin azopolymer film with a thickness below 200 nm. The different NPs concentrations were obtained through different electrospray deposition times varied from 0 to 10 minutes. Birefringence was induced by a He-Cd laser at a wavelength of 442 nm and measured by a probe diode pumped solid state (DPSS) laser at 635 nm. The birefringence dependence on the ZnO NP deposition time reached its maximum for a deposition time of 90 s.

In this study, we employed one of the green synthesis methods utilizing water extracts prepared from solid industrial wastes of Rosa damascena Mill. (RD) and Oriental variety tobacco (Nicotiana tabacum)-mixed stems and leaves (O) as a natural reducing agent for PdCl₂ to obtain environmentally friendly Pd nanoparticles (PdNPs). Transmission electron microscopy (TEM), selected area electron diffraction (SAED), and energy-dispersive X-ray spectroscopy (EDX) in TEM were applied to determine the morphology, microstructure, phase, and elemental composition of PdNPs synthesized. The concentration of PdNPs in the suspensions was quantified by inductively coupled plasma optical emission spectroscopy (ICP-OES), which is essential for their intended application. Furthermore, the synthesized PdNPs were incorporated as dopant into a polymer matrix (PAZO) developed for optical applications. As will be demonstrated, doping PAZO with specific concentrations (0.1, 0.2, 0.25, 0.3, 0.4, 0.5, and 1 wt. %) of green PdNPs enhances the maximal value of the photoinduced birefringence by more than 50%. This improvement enables more efficient inscription of polarization-selective holographic optical elements in the resulting photoanisotropic nanocomposite materials with nearly 25% higher diffraction efficiency. Using a digital polarization holographic setup, the spatial modulation of polarization was recorded on thin nanocomposite films of the azopolymer PAZO, doped with certain concentrations of the green PdNPs.

New bulk chalcogenides from the system (GeTe₆)_1−xCu_x, where x = 5, 10, 15 and 20 mol%, have been synthesized. The structure and composition of the materials were studied using X-ray powder diffraction (XRD) and energy-dispersive spectroscopy (EDS). Scanning electron microscopy (SEM) was applied to analyze the surface morphology of the samples. Some thermal characteristics such as the glass transition, crystallization and melting temperature and some physico-chemical properties such as the density, compactness and molar and free volumes were also determined. The XRD patterns show sharp diffraction peaks, indicating that the synthesized new bulk materials are crystalline. The following four crystal phases were determined: Te, Cu, CuTe and Cu₂GeTe₃. The results from the EDS confirmed the presence of Ge, Te and Cu in the bulk samples in concentrations in good correspondence with those theoretically determined. A layered thin-film material based on Ge₁₄Te₈₁Cu₅, which exhibits lower network compactness compared to the other synthesized new chalcogenides, and the azo polymer PAZO was fabricated, and the kinetics of the photoinduced birefringence at 444 nm was measured. The results indicated an increase in the maximal induced birefringence for the layered structure in comparison to the non-doped azo polymer film.