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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.
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页数:10
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