The corona poling process of electro-optic polymers has been
investigated for rodlike aromatic
polyimides doped with nonlinear optical chromophores. The dynamics
of the chromophores in poling
during and after imidization was observed by measuring second harmonic
generation (SHG) from the
polymer. In the course of poling during imidization, the SHG,
observed before imidization, decreases to
zero, reappears, and increases as the temperature increases. When
poling was after imidization, the
SHG intensity increased monotonically with increasing temperature.
The disappearance of SHG in the
poling during imidization is probably due to the known structural
change in the polymer chains during
imidization and the subsequent reorientation of the chromophores caused
by formation of sheets of
polyimides. The characteristics of the samples poled during and
after imidization are nearly the same
in both the extent of the nonlinear susceptibility and their thermal
stability.
A 6-dimensional grand unified theory with the compact space having the topology of a real projective plane, i.e., a 2-sphere with opposite points identified, is considered. The space is locally flat except for two conical singularities where the curvature is concentrated. One supersymmetry is preserved in the effective 4d theory. The unified gauge symmetry, for example SU(5) , is broken only by the non-trivial global topology. In contrast to the Hosotani mechanism, no adjoint Wilson-line modulus associated with this breaking appears. Since, locally, SU(5) remains a good symmetry everywhere, no UV-sensitive threshold corrections arise and SU(5)-violating local operators are forbidden. Doublettriplet splitting can be addressed in the context of a 6d N = 2 super Yang-Mills theory with gauge group SU(6). If this symmetry is first broken to SU(5) at a fixed point and then further reduced to the standard model group in the above non-local way, the two light Higgs doublets of the MSSM are predicted by the group-theoretical and geometrical structure of the model.
In this study, Eu 3+-doped ZrO 2 nanophosphors were obtained by a solgel method with HNO 3 as a catalyst, which led to white powders of small ZrO 2 nanocrystals after low temperature calcination. However, exothermic reactions of NO 3 ¹ were observed during the heat-treatment leading to ZrO 2 crystallization. To avoid such reactions and to understand the initial crystallization of ZrO 2 doped with Eu 3+ ions, we developed an original route in which the xerogel powders were pre-washed in ethanol before immersing them in Eu 3+ solution to remove NO 3 ¹. The effects of heat-treatment on the Eu 3+ photoluminescence (PL), crystallization of ZrO 2 xerogels, and Eu 3+ localization were studied with PL spectroscopy, thermogravimetric analysis and powder X-ray diffraction. It was found that the amorphous ZrO 2 xerogels crystallized in a tetragonal structure, with a small amount of monoclinic ZrO 2 also being precipitated after longer calcination periods. Finally, the Eu 3+ ions on the surface of the ZrO 2 xerogels were found to diffuse into higher symmetric Zr substitutional sites in the tetragonal ZrO 2 matrix after heat-treatment.
Experimental verification has been carried out the surface tension difference criteria for liquid crystal alignment on solid surfaces. Organic polymer films, with surface tension values controlled from 16.0 to 44.8 mN/m (which includes the surface tension of liquid crystal ZLI-1132) were examined. On films thick enough to avoid undesirable topological effects ( >80 nm), the surface tension value at which the surface changed from a homogeneous to a homeotropic alignment was 31.2 mN/m, which is very close to the 31±0.5 mN/m value of ZLI-1132.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.