Synthesis of CuOx-CeO2 catalyst with high-density interfaces for selective oxidation of CO in H2-rich stream

被引:38
作者
Xu, Changjin [1 ]
Li, Song [1 ]
Zhang, Yue [1 ]
Li, Yijie [1 ]
Zhou, Jun [1 ]
Qin, Gaowu [1 ,2 ]
机构
[1] Northeastern Univ, Sch Mat Sci & Engn, Key Lab Anisotropy & Texture Mat MoE, Shenyang 110819, Liaoning, Peoples R China
[2] Northeastern Inst Met Mat Co Ltd, Shenyang 110108, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Heterogeneous nucleation; High-density interfaces; Copper-cerium based catalysts; CO-PROX; COPPER-CERIA CATALYSTS; ORGANIC FRAMEWORK PRECURSOR; INVERSE CEO2/CUO CATALYSTS; PREFERENTIAL OXIDATION; CUO/CEO2; CATALYSTS; EXCESS H-2; ACTIVE-SITES; PERFORMANCE; FACILE; OXIDE;
D O I
10.1016/j.ijhydene.2018.12.152
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
Constructing materials with high-density interfaces offers a very promising route to enable high-performance nanocatalysts. Herein, a one-pot method to synthetize CuOx-CeO2 spherical catalysts with high-density interfaces is developed by controlling the growth condition so that the CuOx can only nucleate and grow via heterogeneous mode. The synthesis method ensures fine dispersion of CuOx over CeO2 and the density of interface between CuOx and CeO2. The generation of the species of Cu+, Ce3+, and oxygen vacancies are enhanced by the interface interaction. And the reduction of copper ions to metals is effectively suppressed, which helps to avoid deactivation of catalyst at high temperature. When catalyzing the CO preferential oxidation reaction (CO-PROX), the CuOx-CeO2 composite with high-density interfaces exhibits a strikingly high catalytic oxidation activity at a broad operating temperature window (i.e. CO 100% conversion, 95-235 degrees C). The heterogeneous nucleation methodology of synthesizing composite with high-density interfaces reported in this work also applies to other materials system. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4156 / 4166
页数:11
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