نتایج جستجو برای: ultraviolet photoelectron spectrum
تعداد نتایج: 272646 فیلتر نتایج به سال:
We present an extension of the time-dependent configuration-interaction singles (TDCIS) method to the computation of the electron kinetic-energy spectrum in photoionization processes. Especially for strong and long ionizing light pulses, the detection of the photoelectron poses a computational challenge because propagating the outgoing photoelectron wave packet requires large grid sizes. Two di...
A simple method for the synthesis of Nb2O5 films of thicknesses ranging from tens to several hundreds of nanometers on amorphous silicon dioxide or quartz substrates is presented. Nb2O5 films were formed by annealing the sputter deposited Nb films under an Ar flow and without oxygen plasma in a quartz tube within a furnace at 850 C. The structural, compositional, optical, and vibrational proper...
We have obtained photoelectron spectra (PES) for silicon cluster anions with up to 20 atoms. Efficient cooling of species in the source has allowed us to resolve multiple features in the PES for all sizes studied. Spectra for an extensive set of low-energy Si(-)(n) isomers found by a global search have been simulated using density functional theory and pseudopotentials. Except for n = 12, calcu...
In this research zinc sulfide (ZnS) nanoparticles and nanocomposites powders were prepared by chemical precipitation method using zinc acetate and various sulfur sources. The ZnS nanoparticles were characterized by X-ray diffraction, scanning electron microscopy, ultraviolet-visible and fourier transform infra-red. The structure of nanoparticles was studied using X-ray diffraction pattern. The ...
Spectroscopic studies of the SF6- and c-C4F8- anions are reported to provide experimental benchmarks for theoretical predictions of their structures and electron binding energies. The photoelectron spectrum of SF6- is dominated by a long progression in the S-F stretching mode, with an envelope consistent with theoretical predictions that the anion preserves the Oh symmetry of the neutral, but h...
Most large molecules are chiral in their structure: they exist as two enantiomers, which are mirror images of each other. Whereas the rovibronic sublevels of two enantiomers are almost identical (neglecting a minuscular effect of the weak interaction), it turns out that the photoelectric effect is sensitive to the absolute configuration of the ionized enantiomer. Indeed, photoionization of rand...
We present a combined experimental and theoretical study of ruthenium doped germanium clusters, RuGen(-) (n = 3-12), and their corresponding neutral species. Photoelectron spectra of RuGen(-) clusters are measured at 266 nm. The vertical detachment energies (VDEs) and adiabatic detachment energies (ADEs) are obtained. Unbiased CALYPSO structure searches confirm the low-lying structures of anion...
Photoelectron spectroscopy and ab initio calculations have been carried out to probe the structures and chemical bonding of the B27 (-) cluster. Comparison between the experimental spectrum and the theoretical results reveals a two-dimensional (2D) global minimum with a triangular lattice containing a tetragonal defect (I) and two low-lying 2D isomers (II and III), each with a hexagonal vacancy...
Auger photoelectron coincidence spectroscopy (APECS) confirms that a substantial part of the lowenergy tail of the L» VV Auger lines of the 3d transition metals is due to intrinsic initialand final-state shake-up/shake-off processes and not just secondary losses. Data were collected for the L» VV Auger lines of pure Cu, Co, and Ni. APECS enables a direct experimental measurement of the initial-...
The electronic relaxation dynamics of water cluster anions, (H(2)O)(n)(-), have been studied with time-resolved photoelectron imaging. In this investigation, the excess electron was excited through the p<--s transition with an ultrafast laser pulse, with subsequent electronic evolution monitored by photodetachment. All excited-state lifetimes exhibit a significant isotope effect (tau(D)2(O)/tau...
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