Experimental He-pressure broadening for the R(10) and P(2) lines in the ν3 band of CO2, and experimental pressure shifts for R(10) measured at several temperatures between 300 K and 100 K

Helium broadening coefficients for the R(10) and the P(2) lines in the ν₃ band of ¹³CO₂ have been measured over a large range of temperature (70 K-300 K). Helium pressure shifts for the R(10) line at several temperatures between 100 K and 300 K have also been determined. These measurements were obtained with a cold Herriott cell, using the collisional cooling technique to reach the lowest temperatures. They provide an extended dataset for the temperature dependence of widths and shifts. This dataset was compared to theoretical He-broadening coefficients combining quantum scattering calculations and the latest potential energy surface for the system He-CO₂ from Korona et al. [T. Korona, R. Moszynski, F. Thibault, J.-M. Maunay, B. Bussery-Honvault, J. Boissoles, P.E.S. Wormer, J. Chem. Phys. 115 (2001) 3074-3084].     

Optical methods in studies of structural transformations in thin organic films

The examples of phase transitions in Langmuir-Blodgett films of polyvinylidene fluoride (PVDF) and in the surface layer of polystyrene were chosen to demonstrate the great potential of using luminescent molecular probes for studying the heterogeneity of the surfaces of solids and thin films, as well as structural transformations and phase transitions in systems of different natures. The method provides unique information on the local properties of surfaces and thin films when used in combination with other techniques.     

Anomalous vortex dynamics in

We report on measurements of current–voltage (I–V) characteristics for YNi₂B₂C single crystals with weak pinning in various fields at 7.6 K. We find nonmonotonic, N-shaped I–V curves in a certain field region deep in the vortex solid phase. This behavior is anomalous, since there exists an intermediate I region where flow voltage V shows a decrease with increasing I (a driving force). While the exact nature remains unknown, this phenomenon suggests vortex motion (driving I) induced pinning.     

Modeling absorption spectra of molecules in solution

The presence of solvent tunes many properties of a molecule, such as its ground and excited state geometry, dipole moment, excitation energy, and absorption spectrum. Because the energy of the system will vary depending on the solvent configuration, explicit solute–solvent interactions are key to understanding solution-phase reactivity and spectroscopy, simulating accurate inhomogeneous broadening, and predicting absorption spectra. In this tutorial review, we give an overview of factors to consider when modeling excited states of molecules interacting with explicit solvent. We provide practical guidelines for sampling solute–solvent configurations, choosing a solvent model, performing the excited state electronic structure calculations, and computing spectral lineshapes. We also present our recent results combining the vertical excitation energies computed from an ensemble of solute–solvent configurations with the vibronic spectra obtained from a small number of frozen solvent configurations, resulting in improved simulation of absorption spectra for molecules in solution.     

BSA‐Polysaccharide Interactions at Negatively Charged Electrode Surface. Effects of Current Density.

Constant current chronopotentiometric stripping (CPS) peak H due to catalytic hydrogen evolution reaction on Hg‐containing electrodes appeared useful in the analysis of protein complexes with single‐stranded and double‐stranded DNA as well as with peptides. In dependence on stripping current (I_str), structural transition of the protein alone or in complexes can be followed as a result of the protein exposure to electric field effects. For the first time we show here that the CPS analysis can be used for the study of the interaction of BSA with a polysaccharide namely sodium alginate (SA). BSA‐SA complex formation was accompanied by the shift of the structural transition of BSA to lower ‐I_str intensities. Another polysaccharide dextran did not alter I_str‐dependent structural transition of BSA. BSA‐SA complex can be disturbed by an electric field effect or high ionic strength confirming the electrostatic nature of BSA‐SA interaction.     

Spectroscopic estimation of plasma parameters,in the 100–400 ns stage,of a laser-induced plasma in vacuum

This work is focused on the interpretation of the emission spectra in laser-induced plasma observed in the phase at 100–400?ns from after the laser pulse, when the discrete emission lines prevail on the continuum emission, can be important to retrieve the initial stage of expansion. A Q-switched neodymium-doped yttrium aluminum garnet laser has been used for the ablation of a lead sample in vacuum. The observed line profiles, corresponding to different species of lead, were analyzed in terms of delay time. Measurements of parameters of the produced plasmas are performed. The results obtained corroborate the importance of considering nonequilibrium effects in the initial stage of plasma expansion. Also, Stark width for two spectral lines of triply ionized lead is given.     

Implications of spectral hole burning on the manipulation of spatial Goos–Hänchen shift in an atomic cell

We present a new scheme to report on Goos–Hänchen (GH) shift experienced by the Gaussian light beam interacting with an optical cavity filled with four-level sodium atomic medium in the spectral hole burning region with and without Doppler broadening effect. Theoretical atomic density-matrix formalism is employed to obtain the susceptibility of atomic medium while the stationary-phase-theory is used to compute the GH shift in the reflected and transmitted probe beams subjected to control fields. A steep normal slope of dispersion is observed with a maximum and zero probability of transmission and reflection coefficients, respectively, at the regions of the spectral holes burning. In the normal dispersion spectrum at the region of spectral hole burning, positive and negative GH shift is observed, respectively, in the transmitted and reflected light beams. However, at anomalous dispersive regions negative GH shift in the transmission beam and positive GH shift in the reflection beam is observed. The reflection and transmission coefficients as well as the spatial GH shift are the functions of probe detuning, collective phase of control fields, beam incident angle and inverse Doppler broadening effect in the spectral hole burning region. The position and number of spectral holes also depend on the same spectral parametrs as stated above. The study is expected to be useful for optoelectronic devices and optical-clocking applications.     

氩气含量对空气介质阻挡放电发射光谱的影响

利用介质阻挡放电实验系统测量了空气介质阻挡放电的发射光谱,研究了氩气含量对空气介质阻挡放电发射光谱的影响。在280~500 nm波长范围内,发现了氮分子第二正带系Ｎ₂(Ｃ 3Π_ｕ-Ｂ 3Π_ｇ)的谱线和氮分子离子的第一负带系N+₂(B 3Σ＋_ｕ-Ｘ 2Σ＋_ｇ)的谱线。在相同条件下加入10%氩气后,起始放电电压由26 kV降低到23 kV,介质阻挡放电和发射光谱强度都增强,谱线的半宽明显加大。随氩气含量的增加,各个氮分子第二正带系谱线强度的变化趋势不同,而两条氮分子离子第一负带系谱线391.44和427.81 nm的光谱强度都是降低的。     

辅助气燃烧接口对有机化合物碳同位素测定的影响

对多种烷烃及芳香化合物采用不同类型的反应管进行了碳同位素分析, 旨在阐明燃烧接口对有机化合物色谱行为的影响. 结果表明, 在反应管中填充较少的催化剂有助于提高化合物的分离度, 这可能是由于反应管中载气具有较高的线速度, 从而减少了化合物的扩散加宽. 然而, 不同反应管对分离度的改善作用相对有限. 对于不同的反应管, 化合物的灵敏度变化主要与开口分流处分流比的变化有关, 而这种变化可能是由反应管内载气流速的变化所致.     

Tunable monoenergy positron annihilation spectroscopy of polyethylene glycol thin films

Doppler broadening and coincidence Doppler broadening of annihilation radiation experiments have been performed in three kinds of polyethylene glycol(PEG) membrane formed with different average molecular weight using the tunable monoenergy slow positron probe as a function of implantion energy. The obtained positron annihilation parameters are interpreted from two aspects: surface effect and differences in micro-structure or chemical environment of positron annihilation. The experimental results show that the regulation of densification of PEG molecular packing and distribution uniformity from the near surface layer to the bulk region in the film forming process can be well realized by changing its molecular weight. Combining a variable monoenergetic slow positron beam and these two positron annihilation spectroscopy methods is a powerful tool to study positron annihilation characteristics and for polymeric thin-film fine structure analysis.