Recent progress in electrochemical reduction of carbon monoxide toward multi-carbon products

被引:33
作者
Du, Huitong [1 ]
Fu, Jiaju [1 ,5 ]
Liu, Li-Xia [1 ]
Ding, Shichao [2 ]
Lyu, Zhaoyuan [2 ]
Jin, Xin [1 ]
Kengara, Fredrick O. [4 ]
Song, Bing [3 ]
Min, Qianhao [1 ]
Zhu, Jun-Jie [1 ]
Du, Dan [2 ]
Gu, Cheng [1 ]
Lin, Yuehe [2 ]
Hu, Jin-Song [5 ]
Zhu, Wenlei [1 ]
机构
[1] Nanjing Univ, Sch Environm, Sch Chem & Chem Engn, State Key Lab Pollut Control & Resource Reuse, Nanjing 210023, Peoples R China
[2] Washington State Univ, Sch Mech & Mat Engn, Pullman, WA 99164 USA
[3] Scion, Te Papa Tipu Innovat Pk,49 Sala St,Private Bag 302, Rotorua 3046, New Zealand
[4] Bomet Univ Coll, Sch Pure & Appl Sci, Bomet 20400, Kenya
[5] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci BNLMS, Beijing 100190, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Electrochemical CO reduction; Multi -carbon products; Catalysts; Mechanism; SINGLE-ATOM CATALYSIS; CO REDUCTION; POLYCRYSTALLINE COPPER; C-2; PRODUCTS; TRANSITION-METALS; PH-DEPENDENCE; ACTIVE-SITES; LIQUID FUEL; ELECTROREDUCTION; CONVERSION;
D O I
10.1016/j.mattod.2022.08.012
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The increasing CO2 emissions and accompanying climate challenges have boosted the exploration of candidate pathways for storing and utilizing renewable carbon resources. Electrochemical CO2 reduction (ECO2R) has been proven as a promising technology for artificial carbon fixation. Nevertheless, the unsatisfactory multi-carbon (C2+) product selectivity hinders its widespread use. Recently, the indirect route via electrochemical CO reduction (ECOR) to C2+ products has become a potential alternative through the combination with ECO2R. In this review, we briefly summarize the most recent and instructive research in the ECOR development process from advanced ECOR catalysts and reaction mechanisms. Furthermore, the challenges and outlooks based on current understanding in this field are expounded. These insights and perspectives offer meaningful guidance for grasping ECOR and designing relevant catalysts with enhanced C2+ product selectivity.
引用
收藏
页码:182 / 199
页数:18
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