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1.
The electron-stimulated desorption (ESD) of D− and H− ions from condensed D2O and H2O films is investigated. Three low-energy peaks are observed in the ESD anion yield, which are identified as arising from excitation of 2B1, 2A1 and 2B2 dissociative electron attachment (DEA) resonances. Additional structure is observed between 18 and 32 eV, which may be due to ion pair formation or to DEA resonances involving the 2a1 orbital. The ion yield resulting from excitation of the 2B1 resonance increases as the film is heated. We attribute the increase in the ion yield to thermally induced hydrogen bond breaking near the surface, which enhances the lifetimes of the excited states that lead to desorption. 相似文献
2.
Oxygen adsorption on a C-terminated α-Mo2C(0 0 0 1) surface has been investigated with Auger electron spectroscopy, low-energy electron diffraction, and angle-resolved photoemission spectroscopy utilizing synchrotron radiation. It is found that the oxygen atoms adsorb on the Mo atoms in the second layer forming a (1 × 1) orthorhombic periodicity. The oxygen adsorption induces a peculiar state around the Fermi level, which is observed at 0.4 eV in the normal-emission spectra. ARPES measurements show that the state is a partially occupied metallic state. The photoionization cross section of the state shows a maximum at the photon energy of 56 eV, which is assigned as originating from the resonance of the Mo 4d photoemission involving Mo 4p → 4d photoexcitation. 相似文献
3.
A high-resolution angle-resolved photoemission spectroscopy (ARPES) study of Fe(1 1 0) single crystal was conducted to elucidate many-body interactions between quasi-particles at the Fermi level at low-temperature. Two kink structures were observed in the energy-band dispersion at the binding energies of ∼40 meV and ∼270 meV for the bulk-derived band on the majority-spin Fermi surface around the Γ point. Based on analyses of the experimentally obtained real parts of the self-energy, these kink structures are derived from electron-phonon and electron-magnon interactions. 相似文献
4.
Y. Mera 《Surface science》2007,601(22):5207-5211
Reversible polymerization and depolymerization reactions of fullerene (C60) molecules are induced by tunnel injection of holes from tips of scanning tunneling microscopes similarly to the reactions induced by tunneling electrons. The bi-directional and bi-polar features of the hole-induced and electron-induced reactions can be interpreted by a unified model considering ionic reactions over symmetry-imposed barriers in the [2+2] cyclo-addition and the reverse reactions. 相似文献
5.
We compare vibrational, translational and rotational excitations of CO molecules desorbed by electron impact, and the yield of oxygen and carbon atoms from electron-induced fragmentation of CO molecules for: (1) CO monolayers on bare transition metals [Ru(001) and Pt(111)]; (2) CO monolayers coadsorbed with well-ordered oxygen atoms; (3) weakly bound CO monolayers on epitaxially grown silver films; and (4) CO monolayers decoupled from the metallic substrate by mono-atomic xenon spacer layers. For all but the last system, we find CO molecules which are vibrationally extremely hot. This is explained by the excitation of strongly antibonding multi-electron states which are quenched in the vicinity of the metal surface before enough translational energy is acquired by the nuclei to complete dissociation. For CO/Xe/Ag(111), vibrationally hot CO molecules are missing among the desorbing particles, whereas strong fragment signals persist. Because of the isolating Xe layer, the substrate-adsorbate coupling is too weak to terminate the dissociation reaction which is induced by the electron impact before the rupture of the molecular bond. 相似文献
6.
We have measured time-of-flight (TOF) distributions of Br atoms desorbed from thin (less than 1000 Å) epitaxial films of KBr on (100) InSb with a 2 keV electron beam. Although the general structure of the TOF spectra was similar to that obtained previously for the thick crystals, both the fast and the slow (thermal) components of the distribution were strongly dependent on the film thickness. We argue that this dependence is due to two different diffusion processes involved in the transport of the primary excitation products from the bulk to the surface. By measuring the velocity resolved ESD yield for films of various thicknesses, we determined that a diffusion length of the carriers responsible for the thermal ESD component varied from 30 to 700 Å with temperature in the range 20–300°C. In contrast, for the non-thermal desorption we found the carrier diffusion length of about 140 Å which did not depend significantly on the temperature. 相似文献
7.
H. Wadati T. Yoshida A. Chikamatsu H. Kumigashira M. Oshima H. Eisaki 《Phase Transitions》2013,86(8):617-635
Nowadays it has become feasible to perform angle-resolved photoemission spectroscopy (ARPES) measurements of transition-metal oxides with three-dimensional perovskite structures owing to the availability of high-quality single crystals of bulk and epitaxial thin films. In this article, we review recent experimental results and interpretation of ARPES data using empirical tight-binding band-structure calculations. Results are presented for SrVO3 (SVO) bulk single crystals and La1? x Sr x FeO3 (LSFO) and La1? x Sr x MnO3 (LSMO) thin films. In the case of SVO, from comparison of the experimental results with calculated surface electronic structure, we concluded that the obtained band dispersions reflect the bulk electronic structure. The experimental band structures of LSFO and LSMO were analyzed assuming the G-type antiferromagnetic state and the ferromagnetic state, respectively. We also demonstrated that the intrinsic uncertainty of the electron momentum perpendicular to the crystal surface is important for the interpretation of the APRES results of three-dimensional materials. 相似文献
8.
By using angle resolved photoemission spectroscopy, we investigate the electronic structures of Pt-skin layer of Pt–Co and Pt–Ni alloys with CO molecules on the surface. Measured Fermi surface maps and band dispersions reflect the signatures of chemical bonding between Pt-skin layer and CO molecules. Furthermore, the degree of chemical bonding strength of CO molecules, estimated from the energy shift of the participating bands, is found to be reduced on both Pt bimetallic alloys. Our results show how the surface band structure of Pt bimetallic alloys is modified with molecular orbitals of CO molecules on the surface, revealing the important role of the electronic structure in the determination of chemical properties of bimetallic alloys. 相似文献
9.
M. Wanke M. Franz M. Vetterlein G. Pruskil B. Hpfner C. Prohl I. Engelhardt P. Stojanov E. Huwald J.D. Riley M. Dhne 《Surface science》2009,603(17):2808-2814
We report on angle-resolved photoelectron spectroscopy results of thin dysprosium-silicide layers formed on Si(1 1 1), taken with a toroidal analyzer allowing to image the energy surfaces in k||-space. At monolayer dysprosium coverages, where hexagonal DySi2 grows with a 1×1 superstructure, electron pockets are observed at the points with highly anisotropic effective masses, and around a hole pocket at the point also an anisotropic dispersion is found. The band filling of these two bands amounts to one, indicating an even number of electrons assigned to the surface unit cell. Similar features are found for multilayer coverages, where hexagonal Dy3Si5 layers are formed with a superstructure. Here, the influence of zone folding effects due to the reconstructed layers in the bulk silicide is only weak because of the high surface sensitivity of the experiments. 相似文献
10.
The modification of the Au(1 1 1) Shockley-type surface state by an adsorbed monolayer of large π-conjugated molecules was investigated by high-resolution angle-resolved photoelectron spectroscopy (ARPES). We determined binding energy, band mass, and Rashba-splitting and discuss the results in the context of rare-gas adsorption on noble metals. This comparison allows the determination of the bonding strength of the adsorbates, found to be physisorptive with derived binding energies per molecule of 2.0 eV for perylene-tetracarboxylic-dianhydride (PTCDA) and 1.5 eV for naphtalene-tetracarboxylic-dianhydride (NTCDA). We will also present a superstructure model for the NTCDA/Au(1 1 1) system, deduced from low energy electron diffraction images (LEED) in combination with substrate band-backfolding. 相似文献