Insight into the high efficiency of Cu/CeO2 (110) catalysts for preferential oxidation of CO from hydrogen rich fuel

被引:10
|
作者
Wang, Yongke [1 ]
Zhang, Qiuyue [1 ]
Lin, Yuwen [1 ]
Huang, Wujun [1 ]
Ding, Ding [1 ]
Zheng, Yanping [1 ]
Chen, Mingshu [1 ]
Wan, Huilin [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces,Dept Chem, Natl Engn Lab Green Chem Prod Alcohols Ethers Est, Xiamen, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Preferential oxidation of CO in H-2; CO oxidation; Copper based catalyst; Ceria(110); Quasi in-situ XPS and HS-LEIS; AREA CUO-CEO2 CATALYSTS; COPPER-OXIDE; SELECTIVE OXIDATION; CUO/CEO2; CATALYSTS; CARBON-MONOXIDE; CEO2; NANOSHEETS; H-2; SURFACE; CERIUM; IDENTIFICATION;
D O I
10.1016/j.apsusc.2021.150707
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
Ceria nanosheets with predominantly exposing {110} planes had been synthesized, and used as supports to prepare copper-based catalysts for preferential oxidation of CO from hydrogen rich fuel (PROX). The 3 wt% CuO/CeO2 (110) catalyst shows excellent catalytic performance, achieving Con. 100% and Sel. 99.8% at 90 degrees C after a pretreatment with the reaction gas. Quasi in-situ XPS and HS-LEIS results, as well as CO-DRIFTS, reveal that the relative ratio and dispersion of Cu+ on the surface increase after treating with the reaction gas. These results disclose that the interface between Cu+ and CeO2 should play main roles for CO oxidation. The obtained apparent activation energy for hydrogen oxidation is much higher than that for CO oxidation. The selectivity for H-2 oxidation increases significantly and Cu-0 appears concurrently at a higher reaction temperature, leading that Cu-0 is more favor for H-2 oxidation. Therefore, to stabilize Cu+ on CeO2 is the key to achieve high catalytic performance for PROX.
引用
收藏
页数:10
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