Search results for "THEORETICAL-ANALYSIS"
showing 6 items of 6 documents
Stimulated Raman-Spectroscopy of the Q-Branch of Nitrogen at High Pressure - Collisional Narrowing and Shifting in the 150-6800 Bar Range at Room Tem…
1992
0026-8976; The Raman Q branch of N2 has been recorded at room temperature in the pressure range 150-6800 bar, which corresponds to densities from 135 to 800 amagat. In this domain, the Raman Q branch profile is mainly determined by the well-known collisional narrowing. The experimental data have been obtained by means of a high resolution stimulated Raman spectrometer. The linewidth and line shift of the band have been accurately measured as functions of the density, and their density dependences have been fitted by polynomials. The minimum of the linewidth and the maximum of the red shift have been clearly observed at respectively 735.8 and 532.3 amagat. The lineshape was found to be Loren…
Collisional shifting and broadening coefficients for the rovibrational anisotropic lines of the v1/2v2 Fermi dyad in CO2 gas studied by stimulated Ra…
1998
0377-0486; High-resolution stimulated Raman spectroscopy was applied to the study of collisional broadening and shifting for rovibrational anisotropic Raman Lines of the Fermi dyad of molecular carbon dioxide, The O(J) lines of the v1 band and the S(J) lines of the 2v2 band were recorded at 295 K. The pressure-induced line shifts were obtained and compared with the overall shift of the high-density Raman Q-branch, A rotational quantum number dependence of the rovibrational line broadening coefficients was observed. The experimental line broadening coefficients were used in order to check the ability of two theoretical methods (random phase approximation and sum rule) for calculating the lin…
Collisional Broadening, Line Shifting, and Line Mixing in the Stimulated Raman 2-v2 Q-Branch of CH4
1991
0021-9606; Self-, argon-, and helium-broadening coefficients have been measured for 13 lines in the 2v2 Raman Q branch of CH4 using stimulated inverse Raman spectroscopy. The linewidths clearly show the symmetry-state dependence characteristic of pressure broadening, and inelastic processes in general, involving spherical-top molecules. Pressure-induced line shifts have also been measured for these features in pure methane. The pressure-shift coefficients do not display the symmetry-state dependence found for the linewidths. By applying the Rosenkranz perturbation treatment to a pair of collisionally mixed lines, we have been able to obtain an estimate of individual state-to-state contribut…
Nonlinear Raman Spectroscopy in Gases
1992
0022-2860; Recent progress in high-resolution non-linear coherent Raman spectroscopy in the gas phase is reviewed. An instrumental spectral resolution of less than 100 MHz can be routinely achieved. It is limited by the convoluted linewidths of the lasers used for excitation and is of particular advantage in the gas phase, where the rotational structure of vibrational bands is to be resolved. It also allows the measurement of linewidths and line positions with an accuracy of 60 MHz when an appropriate wavemeter is used for calibration. After a short overview of the various techniques being used, examples of recent results of the evaluation of measurements on nitrogen, oxygen, carbon dioxide…
Collisional Raman Linewidths of Nitrogen at High-Temperature (1700-2400 K)
1995
0146-9592; New high-temperature measurements of collisional linewidths of the Roman Q branch of nitrogen have been performed at 1700-2400 K with stimulated Raman spectroscopy in a tungsten filament. We fitted these data together with previous data obtained in the 295-1500-K range to redetermine the parameters of the relaxation models used in coherent anti-Stokes Raman spectroscopy thermometry. The improvement in the accuracy of the temperature measurement has been checked. Semiclassical calculations of linewidths in the 1700-2400-K range agree with the experimental data and have been extended to even higher temperatures.
Pd2Au36(SR)(24) cluster: structure studies
2015
The location of the Pd atoms in Pd2Au36(SC2H4Ph)(24), is studied both experimentally and theoretically. X-ray photoelectron spectroscopy (XPS) indicates oxidized Pd atoms. Palladium K-edge extended X-ray absorption fine-structure (EXAFS) data clearly show Pd-S bonds, which is supported by far infrared spectroscopy and by comparing theoretical EXAFS spectra in R space and circular dichroism spectra of the staple, surface and core doped structures with experimental spectra.