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Title: Electron tunneling of photochemical reactions on metal surfaces: Nonequilibrium Green's function-density functional theory approach to photon energy dependence of reaction probability

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.1902946· OSTI ID:20722927
;  [1]
  1. Department of Chemical System Engineering, Graduate School of Engineering, University of Tokyo, Tokyo 113-8656 (Japan)

We have developed a theoretical model of photoinduced reactions on metal surfaces initiated by the substrate/indirect excitation mechanism using the nonequilibrium Green's function approach. We focus on electron transfer, which consists of (1) electron-hole pair creation, (2) transport of created hot electrons, and (3) tunneling of hot electrons to form an anion resonance. We assume that steps (1), (2), and (3) are separable. By this assumption, the electron dynamics might be restated as a tunneling problem of an open system. Combining the Keldysh time-independent formalism with the simple transport theory introduced by Berglund and Spicer, we present a practical scheme for first-principle calculation of the reaction probability as a function of incident photon energy. The method is illustrated by application to the photoinduced desorption/dissociation of O{sub 2} on a Ag(110) surface by adopting density functional theory.

OSTI ID:
20722927
Journal Information:
Journal of Chemical Physics, Vol. 122, Issue 19; Other Information: DOI: 10.1063/1.1902946; (c) 2005 American Institute of Physics; Country of input: International Atomic Energy Agency (IAEA); ISSN 0021-9606
Country of Publication:
United States
Language:
English