New Design and Construction of Abundant Active Surface Interfacial Copper Entities in CuxCe1-xO2 Nanorod Catalysts for CO-PROX

被引:22
|
作者
Qiu, Zhihuan [1 ]
Guo, Xiaolin [2 ]
Mao, Jianxin [1 ]
Zhou, Renxian [1 ]
机构
[1] Zhejiang Univ, Inst Catalysis, Hangzhou 310028, Zhejiang, Peoples R China
[2] China Jiliang Univ, Coll Mat & Chem, Hangzhou 310018, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC-FRAMEWORK; PREFERENTIAL OXIDATION; SELECTIVE OXIDATION; CUO/CEO2; CATALYSTS; CUO-CEO2; CARBON-MONOXIDE; LOW-TEMPERATURE; EXCESS HYDROGEN; CERIA CATALYSTS; MIXED CU;
D O I
10.1021/acs.jpcc.1c02030
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
Composite CuxCe1-xO2 nanorod catalysts with abundant Cu-Ce interface for CO preferential oxidation are synthesized via a one-pot co-precipitation method at ambient temperature, and then copper species are induced to migrate and enrich on the surface and subsurface of CuxCe1-xO2 by thermal treatment. The best low temperature catalytic activity (T-50% = 77 degrees C) and widest operation window (95-150 degrees C) are achieved by thermal treatment at 700 degrees C. With the thermal treatment temperature increasing from 200 to 700 degrees C, first Cu-Ce solid solution forms (at 400 degrees C), then Cu species migrate to the surface and subsurface of CuxCe1-xO2 nanorods, forming a lattice relaxation layer containing abundant highly dispersed CuOx species and strongly bonded Cu-[O-x]-Ce species, whose thickness is gradually reduced but the tightness is increased, thus strengthening the Cu-Ce interaction. The amount changing and redox process of the active copper entities respectively involving low and high temperature CO-PROX reaction are in-depth clarified.
引用
收藏
页码:9178 / 9189
页数:12
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