雷亚克夫
X射线光电子能谱
铂金
无定形固体
环境压力
氧化物
材料科学
催化作用
化学物理
物理化学
化学工程
化学
分子动力学
计算化学
热力学
结晶学
冶金
有机化学
物理
原子间势
工程类
作者
Donato Fantauzzi,Sandra Krick Calderón,Jonathan E. Mueller,Mathias Grabau,Christian Papp,Hans‐Peter Steinrück,Thomas P. Senftle,Adri C. T. van Duin,Timo Jacob
标识
DOI:10.1002/anie.201609317
摘要
Abstract Detailed knowledge of the structure and degree of oxidation of platinum surfaces under operando conditions is essential for understanding catalytic performance. However, experimental investigations of platinum surface oxides have been hampered by technical limitations, preventing in situ investigations at relevant pressures. As a result, the time‐dependent evolution of oxide formation has only received superficial treatment. In addition, the amorphous structures of many surface oxides have hindered realistic theoretical studies. Using near‐ambient pressure X‐ray photoelectron spectroscopy (NAP‐XPS) we show that a time scale of hours ( t ≥4 h) is required for the formation of platinum surface oxides. These experimental observations are consistent with ReaxFF grand canonical Monte Carlo (ReaxFF‐GCMC) calculations, predicting the structures and coverages of stable, amorphous surface oxides at temperatures between 430–680 K and an O 2 partial pressure of 1 mbar.
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