CO2 photoelectroreduction with enhanced ethanol selectivity by high valence rhenium-doped copper oxide composite catalysts

被引:11
|
作者
Lu, Yueheng [1 ]
Cao, Huazhen [1 ]
Xu, Shenghang [1 ]
Feng, Wenyu [1 ]
Hou, Guangya [1 ]
Tang, Yiping [1 ]
Zhang, Huibin [1 ]
Zheng, Guoqu [1 ]
机构
[1] Zhejiang Univ Technol, Coll Mat Sci & Engn, Hangzhou 310014, Peoples R China
关键词
CuO supported catalyst; High valence rhenium; Photoelectrocatalysis; CO2; conversion; Alcohols; TIO2 NANOTUBE ARRAYS; CARBON-DIOXIDE; PHOTOELECTROCATALYTIC REDUCTION; ELECTROCHEMICAL REDUCTION; PHOTOCATALYTIC REDUCTION; HYDROGEN EVOLUTION; THIN-FILMS; ELECTROREDUCTION; IMMOBILIZATION; PHOTOREDUCTION;
D O I
10.1016/j.jcis.2021.04.087
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
Y CuO supported catalyst with high valence rhenium doping were specially studied for photoelectrocatalytic reduction of CO2 to small molecular alcohols, which were synthesized by nitrate thermal decomposition method on anatase TiO2 nanotube arrays (TiO2-NTs). Photoelectrochemical measurements indicate that the high valence rhenium doping helps in improving the catalytic activity and selectivity of CuO supported catalysts. For the case of 6 wt% Re-doped CuO/TiO2-NTs calcined at 723 K, the principal products are methanol and ethanol with yield up to 19.9 mu mol and 7.5 mu mol after 5 h photoelectrocatalysis at external potential of -0.4 V under simulated solar illumination. In contrast, the products catalyzed by undoped CuO/TiO2-NTs are only methanol and formaldehyde. These results indicate that the high valence rhenium doping will promote the alcoholization process and benefit the C-C coupling, leading to the selective conversion of CO2 to ethanol. Furthermore, under suitable external potential (-0.5 V) the CO2 conversion product is almost entirely composed of ethanol. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:497 / 506
页数:10
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