一氧化碳
锌
催化作用
甲醇
X射线光电子能谱
合金
铜
无机化学
化学状态
纳米颗粒
金属
材料科学
化学
化学工程
冶金
纳米技术
有机化学
工程类
作者
Peter Amann,Bernhard Klötzer,David Degerman,Norbert Köpfle,Thomas Götsch,Patrick Lömker,Christoph Rameshan,Kevin Ploner,Djuro Bikaljević,Hsin‐Yi Wang,Markus Soldemo,Mikhail Shipilin,Christopher M. Goodwin,Jörgen Gladh,Joakim Halldin Stenlid,Mia Börner,Christoph Schlueter,Anders Nilsson
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2022-05-05
卷期号:376 (6593): 603-608
被引量:108
标识
DOI:10.1126/science.abj7747
摘要
The active chemical state of zinc (Zn) in a zinc-copper (Zn-Cu) catalyst during carbon dioxide/carbon monoxide (CO2/CO) hydrogenation has been debated to be Zn oxide (ZnO) nanoparticles, metallic Zn, or a Zn-Cu surface alloy. We used x-ray photoelectron spectroscopy at 180 to 500 millibar to probe the nature of Zn and reaction intermediates during CO2/CO hydrogenation over Zn/ZnO/Cu(211), where the temperature is sufficiently high for the reaction to rapidly turn over, thus creating an almost adsorbate-free surface. Tuning of the grazing incidence angle makes it possible to achieve either surface or bulk sensitivity. Hydrogenation of CO2 gives preference to ZnO in the form of clusters or nanoparticles, whereas in pure CO a surface Zn-Cu alloy becomes more prominent. The results reveal a specific role of CO in the formation of the Zn-Cu surface alloy as an active phase that facilitates efficient CO2 methanol synthesis.
科研通智能强力驱动
Strongly Powered by AbleSci AI