Affiliation:
1. Gintic Institute of Manufacturing Technology, Nanyang Technological University, Singapore 639798, Singapore
2. School of Sciences, Murdoch University, Perth, Western Australia 6150, Australia
Abstract
From the perspective of bond forming, origin of phase-formation on the O-Cu(001) and the O-Cu(110)is analyzed. It is suggested that the formation of the O -1 and the hybridized- O -2 gives in nature the c (2 × 2)-O and subsequently, the [Formula: see text]phase, on the Cu(001). The re-ordering of the primary Cu2O units transforms the Cu(110)-(2×1)-O into the c (6 × 2)-O. As consequences of the O-2 -hybridization, the Cu(001)-[Formula: see text] differs from the Cu(110)-(2×1)-O in origin by nothing more than that the -O-Cu-chain rotates 45° to fit itself to the coordination-surrounding. It proposed that one metal atom may donate more than one-electron to different oxygen atoms. However, one oxygen, with two directional bonding orbitals and two nonbonding orbitals, can never get more than one-electron from a specific metal atom. The sp-hybridization of oxygen cannot occur before its two bonding orbitals are fully occupied. Besides the ionization of oxygen and metal atoms, the polarization of the metal and the hybridization of O -2 dominate the processes of oxidation and the behavior of the oxides. Further considerations are required regarding how the O-coverage reversibly varies the valence-state of oxygen, and how the coverage and temperature reassemble the Cu2O on the Cu(110).
Publisher
World Scientific Pub Co Pte Lt
Subject
Condensed Matter Physics,Statistical and Nonlinear Physics
Cited by
13 articles.
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