多表面相的几何和电子结构:Ni{100}上的碘

D.P. Woodruff
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引用次数: 1

摘要

利用定性LEED、热解吸和俄歇电子能谱法确定了碘在Ni{100}上吸附形成的几种表面相的存在,并根据这些技术的数据提出了这些结构的模型。特别是在室温下,可以发现两个不同的相,一个c(2 × 2)化学吸收相和一个不相称的结构,被确定为轻微扭曲的NiI2单三明治层。加热这些相中的任何一个都会导致一些解吸,并形成一个可变尺寸的中心矩形网状化学吸附相,其特征是碘-碘排斥能的变化。最近使用表面EXAFS、角分辨核和价能级光电发射获得的数据证实了表面碘化物的结构分配,并表明其电子结构基本上与大块NiI2的预期结构一致。讨论了在化学吸收结构范围内光辐射中所见的核心能级结合能变化的研究,并解释为表明该系统中的Ni-I键本质上与I-I - i排斥是共价的,这是由金属相互作用和空间相互作用大致相等的贡献造成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Geometrical and electronic structure of multiple surface phases: Iodine on Ni{100}

The existence of several surface phases formed by the adsorption of iodine on Ni{100} has been established using qualitative LEED, thermal desorption and Auger electron spectroscopy, and models have been proposed for these structures on the basis of data from these techniques. In particular, two different phases can be found at room temperature, a c(2 × 2) chemisorbed phase and an incommensurate structure identified as a slightly distorted single sandwich layer of NiI2. Heating of either of these phases leads to some desorption and the formation of a variable-sized centred rectangular mesh chemisorbed phase characterized by varying iodine- iodine repulsive energies. More recent data obtained using surface EXAFS and angle-resolved core and valence level photoemission confirm the structural assignment for the surface iodide and show its electronic structure to be essentially that expected of bulk NiI2. Studies of core level binding energy changes as seen in photoemission in the range of chemisorbed structures are discussed, and are interpreted as indicating that the Ni-I bond in this system is essentially covalent with the I-I repulsion resulting from roughly equal contributions from through metal and through space interactions.

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