Optical Vortices Generation by Azopolymeric Relief Gratings

The energy and spectral conditions for single-stage holographic recording of a diffraction optical element based on the carbazole-containing azo polymer, that forms singular light beams (optical vortices), have been established. With the atomic-force microscopy (AFM), the surface morphology of the recorded relief holograms was studying, and their diffraction efficiency has been estimated. The topology of the generated optical phase singularities has been studied and the stability range of an optical vortex having the topological charge l = 2 has been found. The possibility of using the developed diffractive optical element in the scheme of optical tweezers for manipulating micro-objects is demonstrated.

Comparative study of photoinduced surface-relief-gratings on azo polymer and azo molecular glass films

A representative azo polymer (BP-AZ-CA) and a typical azo molecular glass (IAC-4) were studied for their surface-relief-grating formation behavior to provide a deep understanding of the clear distinction between these two types of glassy material.

Photoinduced Mass Transport in Azo-Polymers in 2D: Monte Carlo Study of Polarization Effects

We studied the impact of light polarization on photoinduced dynamics of model azo-polymer chains in two dimensions, using bond-fluctuation Monte Carlo simulations. For two limiting models—sensitive to and independent of light polarization—their dynamics driven by photoisomerization of azo-dyes as well as by thermal effects was studied, including characterization of mass transport and chain reorientations. The corresponding schemes of light–matter interaction promote qualitatively different dynamics of photoinduced motion of azo-polymer chains. In particular, they can inhibit or trigger off a directed mass transport along a gradient of light illumination. The generic dynamics of single chains is superdiffusive and is promoted by breaking a symmetry present in the polarization independent model.

Effect of hydrogen-bond strength on photoresponsive properties of polymer-azobenzene complexes

Supramolecular complexation between photoresponsive azobenzene chromophores and a photopassive polymer host offers synthetic and design advantages compared with conventional covalent azo-containing polymers. In this context, it is important to understand the impact of the strength of the supramolecular interaction on the optical response. Herein, we study the effect of hydrogen-bonding strength between a photopassive polymer host [poly(4-vinylpyridine), or P4VP] and three azobenzene analogues capable of forming weaker (hydroxyl), stronger (carboxylic acid), or no H-bonding with P4VP. The hydroxyl-functionalized azo forms complete H-bonding complexation up to equimolar ratio with VP, whereas the COOH-functionalized azo reaches only up to 30% H-bond complexation due to competing acid dimerization that leads to partial phase separation and azo crystallization. We show that the stronger azo-polymer H-bonding nevertheless provides higher photoinduced orientation and better performance during optical surface patterning, in terms of grating depth and diffraction efficiency, when phase separation is either avoided altogether or is limited by using relatively low azo contents. These results demonstrate the importance of the H-bonding strength on the photoresponse of azopolymer complexes, as well as the need to consider the interplay between different intermolecular interactions that can affect complexation.

Tunable Polarization Gratings Based on Nematic Liquid Crystal Mixtures Photoaligned with Azo Polymer-Coated Substrates

Liquid crystal polarization gratings are of great interest for optical communications as elements performing beam steering, splitting, multiplexing or beam combining. Material birefringence, cell thickness or a period of the liquid crystal director pattern influence, among other features, spectroscopic and electro-optical characteristics of fabricated devices, determining thus their functionality and applicability. Here, we report on liquid crystal polarization gratings that allow for complete maximization of the first-order diffraction efficiency (resulting in total elimination of the zeroth-order diffraction) for any wavelength of an incident beam from green to the near-infrared spectral region by applying a low electric voltage. The gratings with periods as small as 10 μm were obtained by holographic exposure of the cell substrates coated with light-sensitive azo polymer alignment layers, and then filled with three different liquid crystal mixtures. The influence of gold nanoparticle dopants in the liquid crystalline mixtures on spectroscopic and electro-optical properties of the devices is presented. Moreover, on the basis of the measured transmittance spectra of the fabricated gratings, the unknown birefringence of liquid crystal mixtures as well as their effective birefringence due to molecular reorientation in the electric field in the visible and near IR region were determined.