离域电子
物理
原子轨道
背景(考古学)
化学吸附
电子
化学键
口译(哲学)
费米面
理论物理学
化学物理
曲面(拓扑)
物理化学
量子力学
化学
吸附
几何学
古生物学
生物
程序设计语言
计算机科学
数学
标识
DOI:10.1103/revmodphys.60.601
摘要
An account is given of a theoretical approach to surface structure and reactivity that is within the framework of solid-state theory, yet strives for chemical ways of interpretation. One begins from highly delocalized band structures, but introduces interpretational tools (density-of-states decompositions, crystal orbital overlap populations) that allow a tracing of local, chemical acts. It is quite feasible to construct interaction diagrams for surfaces, and to make frontier orbital arguments, just as for molecules. There are some interesting ways in which the surface-adsorbate interaction differs from simple molecular binding---in particular, in the way that two-orbital four-electron and zero-electron interactions can turn into bonding. The surface and bulk acting as a reservoir of electrons or holes at the Fermi level are important in this context. Chemisorption emerges as a compromise in a continuum of bonding whose extremes are dissociative adsorption and surface reconstruction.
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