Dephasing of Local Vibrations in a Planar Lattice of Adsorbed Molecules

We investigate anharmonically coupled high- and low-frequency excitations in a planar lattice of adsorbed molecules interacting with phonons of a crystal. Dephasing of high-frequency local vibrations by low-frequency resonance modes is described in terms of temperature Green's function. The equations obtained are solved, first, with a small ratio of the anharmonic coupling coefficient for high- and low-frequency modes to the resonance width, and second, in the low-temperature limit. High-frequency spectral line positions and widths depend on dispersion laws and resonance mode lifetimes. It is shown that lateral interactions of low-frequency modes of adsorbed molecules can lead to a significant narrowing of high-frequency spectral lines, which is consistent with experimental data.Comment: REVTeX, 11 pages, no figure

Photoinduced ordering and anchoring properties of azo-dye films

We study both theoretically and experimentally anchoring properties of photoaligning azo-dye films in contact with a nematic liquid crystal depending on photoinduced ordering of azo-dye molecules. In the mean field approximation, we found that the bare surface anchoring energy linearly depends on the azo-dye order parameter and the azimuthal anchoring strength decays to zero in the limit of vanishing photoinduced ordering. From the absorption dichroism spectra measured in the azo-dye films that are prepared from the azo-dye derivative with polymerizable terminal groups (SDA-2) we obtain dependence of the dichroic ratio on the irradiation dose. We also measure the polar and azimuthal anchoring strengths in nematic liquid crystal (NLC) cells aligned by the azo-dye films and derive the anchoring strengths as functions of the dichroic ratio. Though linear fitting of the experimental data for both anchoring strengths gives reasonably well results, it, in contradiction with the theory, predicts vanishing of the azimuthal anchoring strength at certain nonzero value of the azo-dye order parameter. By using a simple phenomenological model we show that this discrepancy can be attributed to the difference between the surface and bulk order parameters in the films.Comment: revtex4, 25 pages, 9 figure

Kinetics of photoinduced ordering in azo-dye films: two-state and diffusion models

We study the kinetics of photoinduced ordering in the azo-dye SD1 photoaligning layers and present the results of modeling performed using two different phenomenological approaches. A phenomenological two state model is deduced from the master equation for an ensemble of two-level molecular systems. Using an alternative approach, we formulate the two-dimensional (2D) diffusion model as the free energy Fokker-Planck equation simplified for the limiting regime of purely in-plane reorientation. The models are employed to interpret the irradiation time dependence of the absorption order parameters extracted from the available experimental data by using the exact solution to the light transmission problem for a biaxially anisotropic absorbing layer. The transient photoinduced structures are found to be biaxially anisotropic whereas the photosteady and the initial states are uniaxial.Comment: revtex4, 34 pages, 9 figure

Photoinduced 3D orientational order in side chain liquid crystalline azopolymers

We apply experimental technique based on the combination of methods dealing with principal refractive indices and absorption coefficients to study the photoinduced 3D orientational order in the films of liquid crystalline (LC) azopolymers. The technique is used to identify 3D orientational configurations of trans azobenzene chromophores and to characterize the degree of ordering in terms of order parameters. We study two types of LC azopolymers which form structures with preferred in-plane and out-of-plane alignment of azochromophores, correspondingly. Using irradiation with the polarized light of two different wavelengths we find that the kinetics of photoinduced anisotropy can be dominated by either photo-reorientation or photoselection mechanisms depending on the wavelength. We formulate the phenomenological model describing the kinetics of photoinduced anisotropy in terms of the isomer concentrations and the order parameter tensor. We present the numerical results for absorption coefficients that are found to be in good agreement with the experimental data. The model is also used to interpret the effect of changing the mechanism with the wavelength of the pumping light.Comment: uses revtex4 28 pages, 10 figure

Flexible electronics: The next ubiquitous platform

Thin-film electronics in its myriad forms has underpinned much of the technological innovation in the fields of displays, sensors, and energy conversion over the past four decades. This technology also forms the basis of flexible electronics. Here we review the current status of flexible electronics and attempt to predict the future promise of these pervading technologies in healthcare, environmental monitoring, displays and human-machine interactivity, energy conversion, management and storage, and communication and wireless networks

Photoinduced reordering in thin azo-dye films and light-induced reorientation dynamics of nematic liquid-crystal easy axis

We theoretically study the kinetics of photoinduced reordering triggered by linearly polarized (LP) reorienting light in thin azo-dye films that were initially illuminated with LP ultraviolet (UV) pumping beam. The process of reordering is treated as a rotational diffusion of molecules in the light intensity-dependent mean-field potential. The two dimensional diffusion model which is based on the free energy rotational Fokker-Planck equation and describes the regime of in-plane reorientation is generalized to analyze the dynamics of the azo-dye order parameter tensor at varying polarization azimuth of the reorienting light. It is found that, in the photosteady state, the intensity of LP reorienting light determines the scalar order parameter (the largest eigenvalue of the order parameter tensor), whereas the steady state orientation of the corresponding eigenvector (the in-plane principal axis) depends solely on the polarization azimuth. We show that, under certain conditions, reorientation takes place only if the reorienting light intensity exceeds its critical value. Such threshold behavior is predicted to occur in the bistability region provided that the initial principal axis lies in the polarization plane of reorienting light. The model is used to interpret the experimental data on the light-induced azimuthal gliding of liquid-crystal easy axis on photoaligned azo-dye substrates.Comment: 27 pages, 11 fugure

Quenching of CdSe quantum dot emission, a new approach for biosensing

The emission of CdSe quantum dots linked to the 5'-end of a DNA sequence is efficiently quenched by hybridisation with a complementary DNA strand with a gold nanoparticle attached at the 3'-end; contact of the quantum dot and gold nanoparticle occurs