歧化
X射线光电子能谱
催化作用
原子层沉积
化学
密度泛函理论
吸附
物理化学
分析化学(期刊)
无机化学
化学工程
图层(电子)
计算化学
有机化学
工程类
作者
Verena Pramhaas,Matteo Roiaz,Noemi Bosio,Manuel Corva,Christoph Rameshan,Erik Vesselli,Henrik Grönbeck,Günther Rupprechter
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2020-12-17
卷期号:11 (1): 208-214
被引量:40
标识
DOI:10.1021/acscatal.0c03974
摘要
density functional theory (DFT) calculations, we show that the CO reaction onset is determined by a delicate balance between CO disproportionation (Boudouard reaction) and oxidation. CO disproportionation occurs on low-coordinated Pt sites, but only at high CO coverages and when the remaining C atom is stabilized by a favorable coordination. Thus, under the current conditions, initial CO oxidation is found to be strongly influenced by the removal of carbon deposits formed through disproportionation mechanisms rather than being determined by the CO and oxygen inherent activity. Accordingly, at variance with the general expectation, rough Pt nanoparticles are seemingly less active than smoother Pt films. The applied approach enables bridging both the "materials and pressure gaps".
科研通智能强力驱动
Strongly Powered by AbleSci AI