Square-pyramidal subsurface oxygen [Ag4OAg] drives selective ethene epoxidation on silver

被引:32
作者
Chen, Dongxiao [1 ]
Chen, Lin [1 ]
Zhao, Qian-Cheng [1 ]
Yang, Zheng-Xin [1 ]
Shang, Cheng [1 ,2 ]
Liu, Zhi-Pan [1 ,2 ,3 ]
机构
[1] Fudan Univ, Collaborat Innovat Ctr Chem Energy Mat iChEM, Shanghai Key Lab Mol Catalysis & Innovat Mat, Key Lab Computat Phys Sci,Dept Chem, Shanghai, Peoples R China
[2] Shanghai Qi Zhi Inst, Shanghai, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Synthet & Selfassembly Chem Organ Funct Mo, Shanghai, Peoples R China
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
SCANNING-TUNNELING-MICROSCOPY; ETHYLENE EPOXIDATION; PROPYLENE EPOXIDATION; PARTIAL OXIDATION; SURFACE SCIENCE; AG(111); AG; CATALYSIS; REACTIVITY; MECHANISM;
D O I
10.1038/s41929-024-01135-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Ag-catalysed ethene epoxidation is the only viable route for making ethene oxide (EO) in industry, but the active site remains elusive due to the lack of tools to probe this reaction under high temperature and high-pressure conditions. Here, aided by advanced machine-learning grand canonical global structure exploration and in situ experiments, we identify a unique surface oxide phase, namely O5 phase, grown on Ag(100) under industrial catalytic conditions. This phase features square-pyramidal subsurface O and strongly adsorbed ethene, which can selectively convert ethene to EO. The other Ag surface facets, although also reconstructing to surface oxide phases, only contain surface O and produce CO2. The complex in situ surface phases with distinct selectivity contribute to an overall medium (50%) selectivity of Ag catalyst to EO. Our further catalysis experiments with in situ infra-red spectroscopy confirm the theory-predicted infra-red-active C=C vibration of adsorbed ethene on O5 phase and the microkinetics simulation results.
引用
收藏
页码:536 / 545
页数:10
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