X射线光电子能谱
催化作用
化学状态
甲醇
扫描隧道显微镜
纳米颗粒
化学工程
材料科学
相(物质)
化学
纳米技术
有机化学
工程类
作者
Sigmund Jensen,Mathias H. R. Mammen,Martin Hedevang,Zheshen Li,L. Lammich,Jeppe V. Lauritsen
标识
DOI:10.1038/s41467-024-48168-6
摘要
Abstract Methanol formation over Cu/ZnO catalysts is linked with a catalytically active phase created by contact between Cu nanoparticles and Zn species whose chemical and structural state depends on reaction conditions. Herein, we use variable-temperature scanning tunneling microscopy at elevated pressure conditions combined with X-ray photoelectron spectroscopy measurements to investigate the surface structures and chemical states that evolve when a CuZn/Cu(111) surface alloy is exposed to reaction gas mixtures. In CO 2 hydrogenation conditions, Zn stays embedded in the CuZn surface, but once CO gas is added to the mixture, the Zn segregates onto the Cu surface. The Zn segregation is CO-induced, and establishes a new dynamic state of the catalyst surface where Zn is continually exchanged at the Cu surface. Candidates for the migrating few-atom Zn clusters are further identified in time-resolved imaging series. The findings point to a significant role of CO affecting the distribution of Zn in the multiphasic ZnO/CuZn/Cu catalysts.
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