共查询到11条相似文献,搜索用时 78 毫秒
1.
Fluorescence lifetime measurement in the time domain requires excitation from a well separated single bunch using synchrotron light sources. In the colliding mode of the Beijing Electron Positron Collider Ⅱ (BEPCⅡ), a hybrid filling pattern was realized such that a single bunch was placed in the middle of a large gap between two multi-bunch groups. Detection of fluorescence lifetime, based on the excitation of the light pulse from this designated single-bunch, was established at Beamline 4B8 of the Beijing Synchrotron Radiation Facility (BSRF). The timing signal of the BEPCII was utilized as a trigger to gate this fluorescence event. L-Tryptophan amino acid, a known lifetime standard, was selected to assess the lifetime measurement performance. The measured lifetime was consistent in both colliding and single-bunch mode with the time resolution down to 450 ps. Moreover, both the bunch purity and the fine structure of the hybrid filling pattern were characterized. 相似文献
2.
The total electron yield (TEY)mode has been developed successfully for XANES measurements at Beamline 4B7A of BSRF (Beijing Synchrotron Radiation Facility).Its performance was studied by measuring sulphur K-edge XANES of three CdS samples (mixed with graphite powder as an electric conductor)with different concentration:75%,50% and 25%.The data are collected in TEY mode and fluorescence yield (FY)mode respectively for comparison.The results demonstrate that the TEY spectra of three samples agree well with each other after the background is subtracted and normalized.The measured XANES spectra by TEY mode without bias and with 100V bias are almost identical to one another,but the signal-to-noise ratio of spectra measured without bias is better than that with 100V bias.The consistency of the self-absorption corrected FY spectra and TEY spectra are within 10% for the three samples. 相似文献
3.
Ex-situ prepared films of 4-aminothiophenol on Au(1 1 1): photoemission, NEXAFS and STM measurements
V. Arima F. Matino J. Thompson R. Cingolani R. Rinaldi R.I.R. Blyth 《Surface science》2005,580(1-3):63-70
Ex-situ prepared films of 4-aminothiophenol (4-ATP) on Au(1 1 1) have been studied by core-level photoemission using synchrotron radiation, ultra-high-vacuum scanning tunneling microscopy and spectroscopy (UHV-STM, STS), and X-ray absorption (NEXAFS). Photoemission measurements suggest that the film contains a relatively low percentage of 4-ATP bonded to the Au surface, with the presence of free 4-ATP, with oxidised and possibly dimerised molecules also present. We find a lower oxide content than has previously been observed, with well-resolved STM images. These images show a disruption of the long range order of the Au(1 1 1)-(22 × √3) reconstruction, with local nucleation of the reconstruction apparently induced by the 4-ATP, and bias-dependent contrast images. This latter effect, together with the asymmetry observed in STS, is ascribed to the presence of oriented molecular dipole layers between the metal and the organic material. NEXAFS data suggest a broadly upright geometry, with, however, considerable uncertainties. 相似文献
4.
Electron beam melting is being used to modify the microstructure of the surfaces of materials due to its ability to cause localized melting and supercooling of the melt. This article presents an experimental study on the surface modification of Ni-based superalloy (Inconel 625) reinforced with SiC ceramic particles under electron beam melting. Scanning electron microscopy, energy dispersive spectroscopy and X-ray diffraction techniques have been applied to characterize the resulted microstructure. The results revealed growth of novel structures like wire, rod, tubular, pyramid, bamboo and tweezers type morphologies in the modified surface. In addition to that fibrous like structure was also observed. Formation of thin carbon sheet has been found at the regions of decomposed SiC. Electron beam modified surface of Inconel 625 alloy has been hardened twice as compared to the as-received samples. Surface hardening effect may be attributed to both the formation of the novel structures as well as the introduction of Si and C atom in the lattice of Inconel 625 alloy. 相似文献
5.
6.
Alena N. Maratkanova Rishat G. ValeevAlexander V. Syugaev 《Journal of Physics and Chemistry of Solids》2014
Surfactant-assisted ball milling of the Fe powder in paraffin has been used for fabrication of core–shell nanocrystalline particles. The local atomic structure of the bulk and surface layers of the mechanically milled particles has been studied using X-ray absorption spectroscopic techniques with synchrotron radiation from the DORIS storage ring at DESY, Hamburg. Regardless of milling environment composition, the as-prepared powders were shown to be characterized by a significant drop in the EXAFS signal intensity and coordination numbers of the Fe–Fe pairs due to the formation of nanocrystalline state in the particles. It has been shown that an addition of perfluorononanoic acid as a surfactant has a more prominent effect on the structure of the shell layers. The effect is revealed as an appearance of light element atoms (O, F, C) in the local atomic environment of the Fe atoms due to formation of oxide, carbide and adsorbed structures of different types in the particle shell. 相似文献
7.
The interaction between a semi-large aromatic hydrocarbon compound (perylene) and the TiO2(1 1 0)-(1 × 1) surface under ultra high vacuum conditions has been probed by X-ray photoemission spectroscopy (XPS), ultraviolet photoemission spectroscopy (UPS) and near-edge X-ray absorption fine structure (NEXAFS) methods. UPS measurements of the adsorbate system have been compared with an experimental UPS spectrum of perylene in the gas phase and a calculated spectrum obtained by means of density functional theory (DFT) methods. NEXAFS results of perylene molecules adsorbed on TiO2(1 1 0)-(1 × 1) were compared with data from an α-phase perylene single crystal. A novel analysis of the valence data has been employed to show that no strong chemical interaction takes place between perylene and the TiO2(1 1 0)-(1 × 1) surface. Furthermore, angle-dependent NEXAFS measurements and the growth curve results suggest that the perylene molecules are oriented flat down onto the TiO2 substrate due to weak van der Waals interactions. 相似文献
8.
In this work, we study the effect of concentration, host medium, PH and phase states on the fluorescence emission from the
laser dye Rhodamine B pumped by UV laser as exited source. The polymethylmethacrylate PMMA is used as a host medium in case
of solid phase samples while, ethanol and Tetrahydrofuran (THF) are used in case of a liquid one. Laser Induced Fluorescence
(LIF) technique was used to study the fluorescence properties of both cases of liquid and thin film solid-state samples. In
addition, the Dual Thermal Lens (DTL) technique was used to study the quantum yield of these samples. The concentrations of
Rhodamine B in ethanol as solvent between 2 × 10−2 M and 5 × 10−6 M were studied. The maximum fluorescence emission is observed at concentration of Rhodamine B C = 3 × 10−4 M. Comparison studies were investigated for different host medium such as ethanol, THF, PMMA in liquid phase state and PMMA
in solid phase state. The measurements revealed that, the behavior of both phases state was analogous. Rhodamine B/PMMA thin
film sample by ratio of 4:1 and thickness 0.12 mm was found to have the best photostability sample with a quantum yield about
≈0.82. 相似文献
9.
A. Bombardi N. Kernavanois P. Dalmas de Réotier G.H. Lander J.P. Sanchez A. Yaouanc P. Burlet E. Lelièvre-Berna A. Rogalev O. Vogt K. Mattenberger 《The European Physical Journal B - Condensed Matter and Complex Systems》2001,21(4):547-552
In the UxLa1-xS system there is an abrupt loss of the long-range ferromagnetic ordering found in pure US at a critical concentration x
c
∼ 0.57, which is far above the percolation limit. As the magnetic ground state in such a system can be strongly affected by small
variations of the 5f localization, we have investigated a set of samples with different x by polarized neutron diffraction and X-ray magnetic circular dichroism (XMCD). The neutron results are consistent with early
measurements performed on pure US. Even at the lowest U content (x
= 0.15, below x
c
) the shape of the induced form factor (f
(
Q
)) is comparable with that found for x
= 1 and is well reproduced by either a U4+ or a U3+ state. The ratio between the orbital and the effective spin moments in the XMCD measurements confirms this result, but the
evolution of the shape at the M5 edge suggests an abrupt change in the distribution of the electrons (holes) in the 5
f density of states around x
c
.
Received 31 January 2001 相似文献
10.
Effect of local structure on electron paramagnetic resonance spectra for trigonal [Cr(H2O)6]3+coordination complex in the sulfate alums series: a ligand field theory study
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A simple theoretical method is introduced for studying the interrelation between electronic and molecular structures.By diagonalizing the 120 × 120 complete energy matrices,the relationships between zero-field splitting(ZFS) parameter D and local distortion parameter △θ for Cr 3+ ions doped,separately,in α-and β-alums are investigated.Our results indicate that there exists an approximately linear relationship between D and △θ in a temperature range 4.2-297 K and the signs of D and △θ are opposite to each other.Moreover,in order to understand the contribution of spin-orbit coupling coefficient ζ to ZFS parameter D,the relation between D and ζ is also discussed. 相似文献
11.
Fundamental understandings of surface chemistry and catalysis of solid catalysts are of great importance for the developments of efficient catalysts and corresponding catalytic processes, but have been remaining as a challenge due to the complex nature of heterogeneous catalysis. Model catalysts approach based on catalytic materials with uniform and well-defined surface structures is an effective strategy. Single crystals-based model catalysts have been successfully used for surface chemistry studies of solid catalysts, but encounter the so-called “materials gap” and “pressure gap” when applied for catalysis studies of solid catalysts. Recently catalytic nanocrystals with uniform and well-defined surface structures have emerged as a novel type of model catalysts whose surface chemistry and catalysis can be studied under the same operational reaction condition as working powder catalysts, and they are recognized as a novel type of model catalysts that can bridge the “materials gap” and “pressure gap” between single crystals-based model catalysts and powder catalysts. Herein we review recent progress of surface chemistry and catalysis of important oxide catalysts including CeO2, TiO2 and Cu2O acquired by model catalysts from single crystals to nanocrystals with an aim at summarizing the commonalities and discussing the differences among model catalysts with complexities at different levels. Firstly, the complex nature of surface chemistry and catalysis of solid catalysts is briefly introduced. In the following sections, the model catalysts approach is described and surface chemistry and catalysis of CeO2, TiO2 and Cu2O single crystal and nanocrystal model catalysts are reviewed. Finally, concluding remarks and future prospects are given on a comprehensive approach of model catalysts from single crystals to nanocrystals for the investigations of surface chemistry and catalysis of powder catalysts approaching the working conditions as closely as possible. 相似文献