No abstract

Studies on the dynamics of holographic pattern formation in photosensitive polymers, gaining deeper insight into the specific material transformations, are essential for improvements in holographic recording as well as in integrated optics. Here we investigate the kinetics of volume hologram formation in an organic cationic ring-opening polymerization system. The time evolution of the grating strength and the grating phase is presented. We found two steps of growth, separated by a depletion of the light diffraction. Capable to explore this growing behavior, a transition-theory of the refractive index contrast is established. Accordingly the growth curves appear to be ruled by the interplay of polymerization and diffusion. Hence the grating formation mechanisms can be qualified as competing effects regarding the contribution to the refractive index change. We investigate the influence of the preparation and exposure procedure on the transition and consider the usability for integrated wave guide functions.

This chapter aims to establish a link between material compositions, analytical methods and advanced applications for volume holography. It provides basics on volume holography, serving as a compendium on volume holographic grating formation, specific material requirements for volume holography and diffractive properties of the different types of volume holographic gratings. The particular significance of three-dimensional optical structuring for the final optical functionality is highlighted. In this context, the interrelation between function and structure of volume holograms is investigated with view to research on and development of novel materials, methods and applications. Particular emphasis will be placed on analytical methods, assuming that they provide access for a deeper understanding of volume holographic grating formation, which appears to be prerequisite for the design of novel material systems for advanced applications.

This paper targets an inherent control of optical shrinkage in photosensitive polymers, contributing by means of spatially resolved analysis of volume holographic phase gratings. Point by point scanning of the local material response to the Gaussian intensity distribution of the recording beams is accomplished. Derived information on the local grating period and grating slant is evaluated by mapping of optical shrinkage in the lateral plane as well as through the depth of the layer. The influence of recording intensity, exposure duration and the material viscosity on the Bragg selectivity is investigated.

Real-time investigation of Bragg angle shift during volume hologram formation is presented in an organic cationic ring-opening polymerization material. Positive as well as negative values of optical shrinkage are found, assumedly related to mechanical deformations of the volume and a change of the average refractive index, respectively. Ruled by the interplay of polymerization and diffusion, the originate grating formation mechanisms prove to represent competing effects regarding the contribution to the optical shrinkage. The influence of sample preparation and holographic exposure procedure on the effects observed is investigated and the usability for minimization of total Bragg resonance detuning is considered.