催化作用
化学
氧气
扫描隧道显微镜
化学物理
星团(航天器)
氧化物
多相催化
化学计量学
密度泛函理论
结晶学
无机化学
材料科学
纳米技术
物理化学
计算化学
有机化学
生物化学
程序设计语言
计算机科学
作者
Sebastian Kaiser,Farahnaz Maleki,Ke Zhang,W. Harbich,Ueli Heiz,Sergio Tosoni,Barbara A. J. Lechner,Gianfranco Pacchioni,F. Esch
标识
DOI:10.1021/acscatal.1c01451
摘要
Oxidation catalysis on reducible oxide-supported small metal clusters often involves lattice oxygen. In the present work, we trace the path of lattice oxygen from Fe3O4(001) onto small Pt clusters during the CO oxidation, aiming at differentiating whether the reaction takes place at the cluster/support interface or on the cluster. While oxygen vacancies form on many other supports, magnetite maintains its surface stoichiometry upon reduction thanks to a high cation mobility. In order to investigate whether size-dependent oxygen affinities play a role, we study two specific cluster sizes, Pt5 and Pt19. By separating different reaction steps in our experiment, lattice oxygen can be accumulated on the clusters. Temperature programmed desorption (TPD) and sophisticated pulsed valve experiments indicate that the CO oxidation takes place on the Pt clusters rather than at the interface. Scanning tunneling microscopy (STM) shows a decrease in apparent height of the clusters, which density functional theory (DFT) explains as a restructuring following lattice oxygen reverse spillover.
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