Laser-induced concentric colour domains in a cholesteric liquid crystal mixture containing a nematic azobenzene dopant

The isothermal formation of concentric colour domains has been observed in a cholesteric mixture doped with 10 wt % of a photochromic nematic material. The host cholesteric mixture included the Merck materials BL131a and BL130, while the photochromic dopant was a mixture of 4-n-butyl-4′-n-alkoxyazobenzenes (BAAB). The helical pitch of the host cholesteric mixture was increased, as expected, on addition of the photochromic nematic material prior to irradiation with the molecules in the purely trans-configuration. On irradiation with low power (0.6 mW) argon ion laser light, cis-isomers formed within the interaction region and concentric colour domains appeared. Selective reflection from the colour domains occurred in the 400–560 nm spectral range. The coloured domains persisted in the time period following irradiation and extended beyond the interaction region because of diffusion of the cis-isomers. Using the diffusion equation, an expression has been obtained for the average concentration of cis-isomers in each of the coloured domains and the dependence of the reflection wavelength upon the concentration of cis-isomers has been determined.     

Laser-induced concentric colour domains in a cholesteric liquid crystal mixture containing a nematic azobenzene dopant

The isothermal formation of concentric colour domains has been observed in a cholesteric mixture doped with 10 wt % of a photochromic nematic material. The host cholesteric mixture included the Merck materials BL131a and BL130, while the photochromic dopant was a mixture of 4-n-butyl-4'-n-alkoxyazobenzenes (BAAB). The helical pitch of the host cholesteric mixture was increased, as expected, on addition of the photochromic nematic material prior to irradiation with the molecules in the purely trans-configuration. On irradiation with low power (0.6 mW) argon ion laser light, cis-isomers formed within the interaction region and concentric colour domains appeared. Selective reflection from the colour domains occurred in the 400-560 nm spectral range. The coloured domains persisted in the time period following irradiation and extended beyond the interaction region because of diffusion of the cis-isomers. Using the diffusion equation, an expression has been obtained for the average concentration of cis-isomers in each of the coloured domains and the dependence of the reflection wavelength upon the concentration of cis-isomers has been determined.     

Polarization-controlled switching between diffraction orders in transverse-periodically aligned nematic liquid crystals

Transverse-periodic-oriented nematic liquid crystals (LCs) are a special type of optical axis grating that are capable of very high efficiency diffraction (theoretically, 100%) in thin layers of materials with thickness comparable to the radiation wavelength. In particular, they fully diffract linearly polarized input beam into circularly polarized +1st and -1st diffraction orders. We experimentally demonstrate switching between diffraction orders of such gratings when the polarization of the incident beam changes from right-circular to left-circular and vice versa with the aid of an electrically controlled LC phase retarder. Such a setup in which the diffraction efficiency and direction are controlled externally, without application of an electric field to the transverse-periodic grating, provides additional control opportunities and does not compromise the quality of the grating. The grating used in the experiment was 1.5 microm thick and had a period of 4 microm. The contrast ratio of switching between the +1st and -1st orders was as high as 267:1 for a He-Ne laser beam with a switching time of 6.6 ms.     

Q-modulation of a ruby laser oriented by absorbing layers of liquid crystals near the limiting angle of total internal reflection

Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 52, No. 1, pp. 9–16, January, 1990.     

Influence of disorder on superconductivity in non-magnetic rare-earth nickel borocarbides

The effect of substitutional disorder on the superconducting properties of YNi₂B₂C was studied by partially replacing yttrium and nickel by Lu and Pt, respectively. For the two series of (Y, Lu)Ni₂B₂C and Y(Ni, Pt)₂B₂C compounds, the upper critical field H _c2(T) and the specific heat c _p(T, H) in the superconducting mixed state have been investigated. Disorder is found to reduce several relevant quantities such as T _c, the upper critical field H _c2(0) at T=0 and a characteristic positive curvature of H _c2(T) observed for these compounds near T _c. The H _c2(T) data point to the clean limit for (Y, Lu) substitutions and to a transition to the quasi-dirty limit for (Ni, Pt) substitutions. The electronic specific heat contribution γ(H) exhibits significant deviations from the usual linear γ(H) law. These deviations reduce with growing substitutional disorder but remain even in the quasidirty limit which is reached in the Y(Ni_1−x , Pt _x )₂B₂C samples for x=0.1.     

Photosensitive liquid crystals with nanoparticulate internal structure

Stabilization of thermodynamic relaxation of photoinduced cis isomers of azobenzene liquid-crystal molecules is observed in nanoparticulate networks. The phenomenon permits bistability of the phase state (anisotropic and isotropic) of the material and reversible all-optical switching between those states, resulting in strong changes in the light-scattering properties of the material. Recording of complex optical structures with high spatial resolution with the aid of laser beams of different wavelengths is demonstrated.     

Nonlinear refraction in photoinduced isotropic state of liquid crystalline azobenzenes

The photoinduced isotropic state of liquid crystalline azobenzenes exhibits one of the strongest nonlinear optical refraction known for isotropic materials. The optical nonlinearity of these materials is large in a wide band of the visible spectrum and is accompanied with high, over 90%, transmission for red wavelengths.     

Self-activated liquid-crystal cells with photovoltaic substrates

We show that photovoltaic fields are capable of efficiently reorienting liquid crystals, leading to new concepts of optically addressable light modulators. Using an arrangement consisting of a liquid-crystal layer between LiNbO3:Fe photovoltaic substrates, we observed spatial filtering due to self-phase modulation in a planar-oriented cell and nonlinear transmission between crossed polarizers in a twist-oriented cell. These processes do not require an external electric field. The substrates are arranged such that light propagates along the +c axis in each substrate, allowing a secondary process of power transfer to occur through contradirectional photorefractive two-beam coupling.