Optical properties of Tl3SbS3 acousto-optic crystals

Optical properties of acousto-optical material Tl₃SbS₃ were investigated at the fundamental absorption edge. The basic (n = 1) and excited (n = 2, 3) exciton states were obtained from the λ-modulated reflection spectra for polarizations E⊥c at 10 K. Taking into account the spatial dispersion we determined the parameters of excitons by calculating the spectra shapes of λ-modulated reflection of line n = 1 and estimated values of the zone-translation masse and the reduced effective masse of excitons, the effective masse of electrons , heavy and light holes.     

Dependence of photoluminescence from a-Si nanoparticles on the annealing time and exciting wavelength

Thin films of SiO_x having thickness of 0.2 μm and oxygen content x=1.5 or 1.7 are prepared by thermal evaporation of SiO in vacuum. Then some samples are furnace annealed for various times (in the range ) at 770 and 970 K and some others are rapid thermal annealed at 970 K for 30 and 60 s. Photoluminescence (PL) measurements are carried out at room temperature using the 442 nm line of a He-Cd laser and the 488 nm of an Ar laser for excitation. The effect of the annealing conditions and wavelength of the exciting light on the shape of the PL from these films is explored. The deconvolution of the PL spectra measured with the 442 nm line from samples annealed at 770 K for reveals two distinct PL bands peaked at around 2.3 and 2.5 eV, which do not shift appreciably with increasing annealing time. In addition, at longer annealing times, a weak third band is resolved centred in the range 2.0-2.1 eV. It exists in the spectra of all samples annealed at 970 K being more prominent in the samples with x=1.5. The intensity of this band shows different dependences on the annealing time in the films with different initial composition. The results obtained are discussed in terms of radiative recombination via defect states in the SiO_x matrix (the 2.5 eV band) or at the a-Si-SiO_x interface (the 2.3 eV band). The band centred in the 2.0-2.1 eV range is related to recombination in amorphous silicon nanoparticles grown upon annealing.     

On a possible variation of the proton-to-electron mass ratio: H2 spectra in the line of sight of high-redshift quasars and in the laboratory

Recently the finding of an indication for a decrease of the proton-to-electron mass ratio μ = m_p/m_e by 0.002% in the past 12 billion years was reported in the form of a Letter [E. Reinhold, R. Buning, U. Hollenstein, P. Petitjean, A. Ivanchik, W. Ubachs, Phys. Rev. Lett. 96 (2006) 151101]. Here we will further detail the methods that led to that result and put it in perspective. Laser spectroscopy on molecular hydrogen, using a narrow-band and tunable extreme ultraviolet laser system at the Laser Centre Vrije Universiteit Amsterdam, results in transition wavelengths of spectral lines in the Lyman and Werner band systems at an accuracy of (4-11) × 10⁻⁸, depending on the wavelength region. This corresponds to an absolute accuracy of 0.000004-0.000010 nm. A database of 233 accurately calibrated H₂ lines is presented here for future reference and comparison with astronomical observations. Recent observations of the same spectroscopic features in cold hydrogen clouds at redshifts z = 2.5947325 and z = 3.0248970 in the line of sight of two quasar light sources (Q 0405−443 and Q 0347−383) resulted in 76 reliably determined transition wavelengths of H₂ lines at accuracies in the range 2 × 10⁻⁷ to 1 × 10⁻⁶. Those observations were performed with the Ultraviolet and Visible Echelle Spectrograph at the Very Large Telescope of the European Southern Observatory at Paranal, Chile. A third ingredient in the analysis is the calculation of an improved set of sensitivity coefficients K_i, a parameter associated with each spectral line, representing the dependence of the transition wavelength on a possible variation of the proton-to-electron mass ratio μ. The new model for calculation of the K_i sensitivity coefficients is based on a Dunham representation of ground state and excited state level energies, derived from the most accurate data available in literature for the ground electronic state and the presently determined level energies in the and C¹Π_u states. Moreover, the model includes adiabatic corrections to electronic energies as well as local perturbation effects between B and C levels. The full analysis and a tabulation of the resulting K_i coefficients is given in this paper. A statistical analysis of the data yields an indication for a variation of the proton-to-electron mass ratio of Δμ/μ = (2.45 ± 0.59) × 10⁻⁵ for a weighted fit and Δμ/μ = (1.99 ± 0.58) × 10⁻⁵ for an unweighted fit. This result, indicating the decrease of μ, has a statistical significance of 3.5σ. Mass-variations as discussed relate to inertial or kinematic masses, rather than gravitational masses. Separate treatment of the data gives a similar positive result for each of the quasars Q 0405−443 and Q 0347−383. The statistical analysis is further documented and possible systematic shifts underlying the data, with the possibility of mimicking a non-zero Δμ/μ value, are discussed. The observed decrease in μ corresponds to a rate of change of d lnμ/dt = −2 × 10⁻¹⁵ per year, if a linear variation with time is assumed. Experiments for detecting a possible variation of μ in the modern epoch via ultra-precision experiments on H₂ quadrupole transitions are proposed.     

On the formulation of D = 11 supergravity and the composite nature of its three-form gauge field

The underlying gauge group structure of the D = 11 Cremmer-Julia-Scherk supergravity becomes manifest when its three-form field A₃ is expressed through a set of one-form gauge fields, , , η_1α, and E^a, ψ^α. These are associated with the generators of the elements of a family of enlarged supersymmetry algebras parametrized by a real number s. We study in detail the composite structure of A₃ extending previous results by D’Auria and Fré, stress the equivalence of the above problem to the trivialization of a standard supersymmetry algebra E^(11|32) cohomology four-cocycle on the enlarged superalgebras, and discuss its possible dynamical consequences. To this aim we consider the properties of the first order supergravity action with a composite A₃ field and find the set of extra gauge symmetries that guarantee that the field theoretical degrees of freedom of the theory remain the same as with a fundamental A₃. The extra gauge symmetries are also present in the so-called rheonomic treatment of the first order D = 11 supergravity action when A₃ is composite. Our considerations on the composite structure of A₃ provide one more application of the idea that there exists an extended superspace coordinates/fields correspondence. They also suggest that there is a possible embedding of D = 11 supergravity into a theory defined on the enlarged superspace .     

Investigation of nonlinear optical properties of organic dye by Z-scan technique using He-Ne laser

The third-order nonlinear optical properties of Basic Green 1 dye were measured by the Z-scan technique and measurements were carried out at different concentrations and several incident intensities. The results showed that the Basic Green 1 dye exhibited large nonlinear refractive coefficient () and nonlinear absorption coefficient () at the wavelength 632.8 nm of He-Ne. The negative sign of the nonlinear refractive index n₂ indicates that this material exhibits self-defocusing optical nonlinearity. These results show that Basic Green 1 dye has potential applications in nonlinear optics.     

Photoisomerization dynamics study on cis-azobenzene derivative using ultraviolet-to-visible tunable femtosecond pulses

We performed the transient absorption measurement and the first rate equation (RE) analysis for cis isomer of 4-carboxy-2′,6′-dimethylazobenzene to clarify the quantitative difference between the photoisomerization process and the thermal relaxation process from the excited state. The RE analysis enabled us to determine the cis-to-trans photoisomerization rate per each pump pulse to be 3% under the condition of the 430 nm, 150 fs pump pulse with energy of 200 nJ. Moreover, the signal due to the yielded trans molecules appearing in the transient absorption was assigned from the following observed result: the transient absorbance change at the 380 nm probe mostly decreased within 300 fs after the 430 nm pulse pumping and then slowly decreased to zero, while the absorbance change at the 350 nm probe had a positive constant component in the over one picosecond time region. The RE analysis showed that this constant component is due to the yielded trans molecules, and its positive value is due to the fact that the absorption cross-section of the -to- transition in their trans molecules is larger than that of the -to- transition in the original cis molecules.     

Dielectric relaxation in single crystal NH4H2PO4 in the high-temperature regime

The dispersion curves of the dielectric response in single crystal NH₄H₂PO₄ were obtained in the radio frequency range and below the high-temperature transition at T_p−160 °C. The results reveal dielectric relaxation at low frequency, which is about 10⁵ Hz at 70 °C, and it shifts to higher frequencies (∼3×10⁶ Hz) as the temperature increases. The relaxation frequency was determined from the peak obtained in the imaginary part of the permittivity as well as from the derivative of the real part of the permittivity. The activation energy E_a=0.55 eV, obtained from the relaxation frequency is very close to that derived from the dc conductivity. We suggest that this dielectric relaxation could be due to the proton jump and phosphate reorientation that cause distortion and change the local lattice polarizability inducing dipoles like      

Fluorescence and solvatochromism of a merocyanine dye with a high quadratic polarizability in solutions and polymer films

The influence of medium polarity on the spectroscopic and photophysical properties of 2-[(2E,4E)-6-(1,3,3-trimethyl-2,3-dihydro-1H-2-indolyliden)-2,4-hexadienyliden]malononitrile (THDM) in solutions and polymer matrices is studied at room temperature and 77 K under conditions of steady-state and pulsed laser excitation. A large bathochromic shift of the absorption spectra observed upon an increase in the solvent polarity is caused by a strong increase of the dipole moment in the ground state () on going to an excited Franck-Condon state (). Based on the solvatochromic data, the quadratic polarizability was calculated to be , which is close to the experimentally determined value . A strong narrowing of the fluorescence spectra in comparison with the absorption spectra at room temperature is observed upon an increase in the solvent polarity caused by a decrease in the bond length alternation parameter and by weakening of vibronic interactions in the singlet excited state. The mirror symmetry of the absorption and fluorescence spectra of THDM in ethanol at 77 K is explained by the increase of the electrostatic interactions between the solvent and merocyanine molecules. The dynamic fluorosolvatochromism of THDM in the picosecond range is caused by molecules reorientations of the polar environment occurring during a time period consistent with the dielectric relaxation time of these molecules.     

Measurements of insulator band parameters using combination of single-electron and two-electron spectroscopy

We describe the application of low energy time-of-flight coincidence (e,2e) spectroscopy for measurements of the energy band parameters of a dielectric. The (e,2e) spectrometer can operate also in a single-electron mode by switching off coincidence conditions, and can be used for recording electron energy loss spectra (EELS). Thus, the combination of (e,2e) and EELS allows the measurement of energy gap E_g, valence bandwidth ΔE_val, electron affinity χ and excitonic levels position E_ex of a dielectric. The energy band parameters of LiF film deposited on Si(001) surface are measured: ΔE_val=      

Mott-type hopping conduction in the ordered and disordered phases of LiCoO2

The temperature dependence of dc resistance was observed in the range of for layered-rock-salt (hexagonal structure, ordered distribution between Li and Co) and modified-spinel (cubic, random distribution) phases of LiCoO₂. The results suggest Mott-type hopping conduction arising from the localized Co-3d electrons in the valence band. The densities of states (DOS) at the Fermi energy (E_F) estimated from the slope of the resistance curves were 2.0×10²⁰ and 5.5×10¹⁹ cm⁻³ eV⁻¹ for the ordered and disordered phases, respectively. The relatively low DOS at E_F in the disordered phase suggests that E_F approaches the edge of the valence band as a result of the narrowing of Co-t_2g bands due to the higher lattice symmetry in the disordered phase.