Very high loading oxidized copper supported on ceria to catalyze the water-gas shift reaction

被引:30
作者
Yu, Wen-Zhu [1 ]
Wang, Wei-Wei [1 ]
Ma, Chao [2 ]
Li, Shan-Qing [3 ]
Wu, Ke [4 ]
Zhu, Jin-Ze [1 ]
Zhao, Hao-Ran [1 ]
Yan, Chun-Hua [4 ,5 ]
Jia, Chun-Jiang [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, Key Lab Special Aggregated Mat, Jinan 250100, Peoples R China
[2] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Peoples R China
[3] Chizhou Univ, Dept Chem & Mat Engn, Chizhou 247000, Peoples R China
[4] Peking Univ, Beijing Natl Lab Mol Sci, State Key Lab Rare Earth Mat Chem & Applicat, PKU HKU Joint Lab Rare Earth Mat & Bioinorgan Che, Beijing 100871, Peoples R China
[5] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
基金
美国国家科学基金会;
关键词
Active oxidized Cu sites; Oxygen diffusion; Activation effect; The water-gas shift reaction; CO OXIDATION; IN-SITU; X-RAY; OXIDE CLUSTER; ACTIVE-SITES; SURFACE; OXYGEN; CEO2; RAMAN; CU;
D O I
10.1016/j.jcat.2021.08.024
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
To prepare supported catalysts with high loading and high dispersion of active metals is a crucial chal-lenge in heterogeneous catalysis. Here we report the fabrication of very reactive catalyst that contains finely dispersed copper with 20 wt% content supported on high-surface area CeO2 for the water-gas shift (WGS) reaction. This copper-ceria catalyst shows superb activity with a CO consumption rate of 116.7 lmolCO gcat-1 s-1 at 300 celcius, nearly one order of magnitude more active than other copper-based catalysts ever reported. Based on the precise and integrated characterizations, the oxidized not the metallic Cu are proved to be active centers where the adsorbed CO directly reacted with bridged -OH groups to finish the WGS reaction. The oxidized Cu sites are confirmed to be originated from the activation effect from Cu to CeO2, which promotes the oxygen of CeO2 diffuse from the bulk to surface, making Cu oxidized even under reductive atmosphere. (c) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:83 / 93
页数:11
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