Experimental and theoretical investigation of the electronic structure of Cu2O and CuO thin films on Cu(110) using x-ray photoelectron and absorption spectroscopy

被引:275
作者
Jiang, Peng
Prendergast, David [1 ]
Borondics, Ferenc [2 ]
Porsgaard, Soeren [3 ]
Giovanetti, Lisandro
Pach, Elzbieta
Newberg, John [2 ]
Bluhm, Hendrik [2 ]
Besenbacher, Flemming [3 ]
Salmeron, Miquel [4 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Mat Sci, Mol Foundry, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
[3] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[4] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
关键词
COPPER-BASED CATALYSTS; AMBIENT-PRESSURE; METHANOL; OXYGEN; OXIDATION; SURFACE; REDUCTION; SPECTRA; OXIDES; DECOMPOSITION;
D O I
10.1063/1.4773583
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
The electronic structure of Cu2O and CuO thin films grown on Cu(110) was characterized by X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS). The various oxidation states, Cu-0, Cu+, and Cu2+, were unambiguously identified and characterized from their XPS and XAS spectra. We show that a clean and stoichiometric surface of CuO requires special environmental conditions to prevent loss of oxygen and contamination by background water. First-principles density functional theory XAS simulations of the oxygen K edge provide understanding of the core to valence transitions in Cu+ and Cu2+. A novel method to reference x-ray absorption energies based on the energies of isolated atoms is presented. (C) 2013 American Institute of Physics. [http://dx.doi.org/10.1063/1.4773583]
引用
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页数:6
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