Hierachical Aerogel-Supported Cu-Sn-Ox Solid Solutions for Highly Selective CO2 Electroreduction and Zn-CO2 Batteries

被引:0
|
作者
Wang, Nan [1 ,2 ]
Mei, Riguo [2 ]
Zhang, Guobin [2 ]
Chen, Liqiong [2 ]
Yang, Tao [2 ]
Chen, Zhongwei [2 ,3 ]
Lin, Xidong [2 ]
Liu, Qingxia [1 ,2 ,4 ]
机构
[1] Shenzhen Univ, Coll Appl Sci, Shenzhen 518060, Peoples R China
[2] Shenzhen Technol Univ, Future Technol Sch, Shenzhen 518118, Peoples R China
[3] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[4] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB, Canada
基金
中国国家自然科学基金;
关键词
aerogel; solid solution; CO2; reductionreaction; selectivity to HCOOH; Zn-CO2; battery; ELECTROCHEMICAL REDUCTION; OXYGEN VACANCIES; OXIDE; EFFICIENT; SITES; GAS; NANOCRYSTALS; PERFORMANCE; CATALYSTS; FORMATE;
D O I
10.1021/acsami.4c06157
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The electrochemical CO2 reduction reaction (CO2RR) into high-value carbon compounds such as CO and HCOOH is a promising strategy for the utilization and conversion of emitted CO2. However, the selectivity of the CO2RR for HCOOH is typically less than 90% and operates within a narrow voltage range, which limits its practical application. Herein, we propose a novel heterostructural aerogel as a highly efficient electrocatalyst for CO2RR to HCOOH. This catalyst consists of Cu-Sn-O-x solid solutions embedded in a reduced graphene oxide matrix (Cu-Sn-O-x/rGO). The incorporation of Cu2+ into the SnO2 matrix enhances HCOOH production by improving the adsorption of the *OCHO intermediate and inhibiting H-2 evolution, as confirmed by in situ measurements and computational studies. As a result, Cu-Sn-O-x/rGO achieves a remarkable Faradaic efficiency (FE) of up to 91.4% for HCOOH and maintains high selectivity over a broad operating voltage range (-0.8 to -1.1 V). Additionally, the assembled Zn-CO2 batteries demonstrated an excellent power density of 1.14 mW/cm(2) and exceptional stability for over 25 h.
引用
收藏
页码:42128 / 42137
页数:10
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