Oxidation of Pt(111) under Near-Ambient Conditions

被引:155
作者
Miller, D. J. [1 ,2 ]
Oberg, H. [3 ]
Kaya, S. [2 ]
Casalongue, H. Sanchez [2 ]
Friebel, D. [1 ,2 ]
Anniyev, T. [1 ,2 ]
Ogasawara, H. [2 ]
Bluhm, H. [4 ,5 ]
Pettersson, L. G. M. [3 ]
Nilsson, A. [1 ,2 ,3 ]
机构
[1] Stanford Inst Mat & Energy Sci, SLAC Natl Accelerator Lab, Menlo Pk, CA 94025 USA
[2] SLAC Natl Accelerator Lab, Stanford Synchrotron Radiat Lightsource, Menlo Pk, CA 94025 USA
[3] Stockholm Univ, AlbaNova Univ Ctr, Dept Phys, S-10691 Stockholm, Sweden
[4] Univ Calif Berkeley, Lawrence Berkeley Lab, Adv Light Source, Berkeley, CA 94720 USA
[5] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 USA
关键词
ATOMIC OXYGEN; GAS-PHASE; SPECTROSCOPY; SURFACE; OXIDE; KINETICS;
D O I
10.1103/PhysRevLett.107.195502
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The oxidation of Pt(111) at near-ambient O-2 pressures has been followed in situ using x-ray photoelectron spectroscopy (XPS) and ex situ using x-ray absorption spectroscopy (XAS). Polarization-dependent XAS signatures at the O K edge reveal significant temperature-and pressure-dependent changes of the Pt-O interaction. Oxide growth commences via a PtO-like surface oxide that coexists with chemisorbed oxygen, while an ultrathin alpha-PtO2 trilayer is identified as the precursor to bulk oxidation. These results have important implications for understanding the chemical state of Pt in catalysis.
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页数:5
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