Design of Cu/MoOx for CO2 Reduction via Reverse Water Gas Shift Reaction

被引:3
|
作者
Gao, Yuan [1 ]
Xiong, Kun [1 ]
Zhu, Bingfeng [2 ]
机构
[1] Chongqing Technol & Business Univ, Engn Res Ctr Waste Oil Recovery Technol & Equipmen, Sch Environm & Resources, Minist Educ, Chongqing 400067, Peoples R China
[2] Pharmaceut Coll, Affiliated Hosp Chongqing Med 1, Chongqing 400060, Peoples R China
关键词
CO2; reduction; reverse water-gas shift; Cu-MoOx; interaction; catalytic performance; SOLID-SOLUTION; HYDROGENATION; CATALYSTS; METHANOL; PERFORMANCE; MECHANISM; VACANCIES; WELL;
D O I
10.3390/catal13040684
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
CO2 reduction to CO as raw material for conversion to chemicals and gasoline fuels via the reverse water-gas shift (RWGS) reaction is generally acknowledged to be a promising strategy that makes the CO2 utilization process more economical and efficient. Cu-based catalysts are low-cost and have high catalytic performance but have insufficient stability due to hardening at high temperatures. In this work, a series of Cu-based catalysts supported by MoOx were synthesized for noble metal-free RWGS reactions, and the effects of MoOx support on catalyst performance were investigated. The results show that the introduction of MoOx can effectively improve the catalytic performance of RWGS reactions. The obtained Cu/MoOx (1:1) catalyst displays excellent activity with 35.85% CO2 conversion and 99% selectivity for CO at 400 degrees C. A combination of XRD, XPS, and HRTEM characterization results demonstrate that MoOx support enhances the metal-oxide interactions with Cu through electronic modification and geometric coverage, thus obtaining highly dispersed copper and more Cu-MoOx interfaces as well as more corresponding oxygen vacancies.
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页数:11
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