Eliminating ground-state dipole moments in quantum optics via canonical transformation

By means of a canonical transformation it is shown how it is possible to recast the equations for molecular nonlinear optics to completely eliminate ground-state static dipole coupling terms. Such dipoles can certainly play a highly important role in nonlinear optical response - but equations derived by standard methods, in which these dipoles emerge only as special cases of transition moments, prove unnecessarily complex. It has been shown that the elimination of ground-state static dipoles in favor of dipole shifts results in a considerable simplification in form of the nonlinear optical susceptibilities. In a fully quantum theoretical treatment the validity of such a procedure has previously been verified using an expedient algorithm, whose defense was afforded only by a highly intricate proof. In this paper it is shown how a canonical transformation method entirely circumvents such an approach; it also affords new insights into the formulation of quantum field interactions.Comment: 18 pages including 1 figur

Photoluminescent Thin Films of Room-Temperature Glassy Tris(keto-hydrozone) Discotic Liquid Crystals and Their Nanocomposites with Single-Walled Carbon Nanotubes for Optoelectronics

This study addresses the photoresponse of liquid-crystalline tris(keto-hydrozone) discotic (TKHD)a star-shaped molecular structure with three branches. Object of our research interest was also TKHD filled with single-walled carbon nanotubes (SWCNTs) at a concentration of 1 wt %. At room temperature, the discotic liquid crystals in thin films (thickness 3 μm) of both TKHD and nanocomposite SWCNT/TKHD were in a glassy state. Such glassy thin films exhibited photoluminescence ranging from the deep-red to the near-infrared spectral region, being attractive for organic optoelectronics. The addition of SWCNTs to TKHD was found to stabilize the photoluminescence of TKHD, which is of significance for optoelectronic device applications. The photothermoelectrical response of highly conductive SWCNT/TKHD nanocomposite films was characterized by electrical impedance spectroscopy in the frequency range from 1 Hz to 1 MHz of the applied electric field. It was elucidated that the reversible photothermoelectrical effect in SWCNT/TKHD films occurs through SWCNTs and their network

Ion-Conducting Flexible Thin Films of Composites from Poly(ethylene oxide) and Nematic Liquid Crystals E8—Characterization by Impedance and Dielectric Relaxation Spectroscopy

Complex electrical impedance and dielectric spectroscopy were applied to study the dielectric relaxations and their thermal behavior in ion-conducting composites/complexes from polymer poly(ethylene oxide) (PEO) and E8 nematic liquid crystals (LCs), at the compositional ratio PEO:E8 = 70:30 wt%. Flexible thin films of PEO/E8 with a thickness of 150 μm were inspected, as well as such films from Na+ ion-conducting electrolyte PEO/E8/NaIO4 with the same PEO:E8 compositional ratio, but additionally containing 10 wt.% from the salt sodium metaperiodate (NaIO4) as a dopant of Na+ ions. The molecular dynamics, namely the dielectric relaxation of PEO/E8 and PEO/E8/NaIO4, were characterized through analyses of complex impedance and dielectric spectra measured in the frequency range of 1 Hz–1 MHz, under variation of temperature from below to above the glass-transition temperature of these composites. The relaxation and polarization of dipole formations in PEO/E8 and PEO/E8/NaIO4 were evidenced and compared in terms of both electrical impedance and dielectric response depending on temperature. The results obtained for molecular organization, molecular relaxation dynamics, and electric polarization in the studied ion-conducting polymer/LC composites/complexes can be helpful in the optimization of their structure and performance, and are attractive for applications in flexible organic electronics, energy storage devices, and mechatronics

SODIUM-ION-CONDUCTING POLYMER NANOCOMPOSITE ELECTROLYTE OF TIO2/PEO/PVP COMPLEXED WITH NАIO4

Investigation on Sodium-ion-conducting polymer nanocomposite electrolyte system based on the polymer blend of poly(ethylene oxide) and polyvinyl pyrrolidone (PEO/PVP), complexed with NaIO4 salt and nanofilled with TiO2 of average size ~10 nm, are presented in this report. The salt complexed polymer blend electrolytes were prepared in the form of dimensionally stable and free-standing thin films (150 μm) by conventional solution cast technique. In the polymer blend, the PEO proportion was 70 weight percent (wt%). In PEO/PVP polymer matrix, the salt NaIO4 and the TiO2 nanofiller were at concentration of 10 wt% and 1 wt%, respectively. Micro Raman and XRD studies confirmed the miscibility between PEO and PVP and the complexation of the salt with PEO/PVP polymer host. TEM measurements were carried out to evaluate the size and distribution of the dispersed TiO2 nanofillers. The complex impedance spectroscopy in the frequency range 1 Hz – 1 MHz at room temperature shows an enhanced ionic conductivity of the four-component PEO/PVP/NaIO4/TiO2 nanocomposite Sodium-ion-conducting polymer electrolyte system