Surface coordination of adatoms by scanned low energy photoelectron diffraction

被引:3
作者
Asensio, MC [1 ]
机构
[1] CTR UNIV PARIS SUD,UTILISAT RAYONNEMENT ELECTROMAGNET LAB,F-91405 ORSAY,FRANCE
关键词
X-RAY-PHOTOELECTRON; MULTIPLE-SCATTERING APPROACH; AUGER-ELECTRON DIFFRACTION; RESOLVED PHOTOEMISSION; INDUCED RELAXATIONS; TILTED CO; NI(111); RESOLUTION; OXYGEN; LEED;
D O I
10.1142/S0218625X97000298
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this article, a brief overview of the current activity in the field of low energy photoelectron diffraction is presented. Although alternatively angle and energy-scanned photoelectron diffraction can be used to obtain the surface-structural information, we limit our discussion to the low energy and energy-scanned modes and their use in connection with anew developed direct method. By the use of this most recent approach, adatom-substrate distances and adsorption sites are directly revealed from a discrete mapping of the Fourier transform of scanned energy photoelectron diffraction spectra, measured at a representative set of geometries, which depend on the symmetry of the particular studied system. In addition, a short discussion on the determination of the detailed structure of adsorbed overlayers by the traditional trial-and-error method is included, using model multiple scattering calculations. These latest developments are illustrated with a specific example of an atomic adsorbate, and comments about the capabilities and limitations of photoelectron diffraction as a structural technique in new fields.
引用
收藏
页码:295 / 305
页数:11
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