Engineering Bismuth-Tin Interface in Bimetallic Aerogel with a 3D Porous Structure for Highly Selective Electrocatalytic CO2 Reduction to HCOOH

被引:307
作者
Wu, Zexing [1 ]
Wu, Hengbo [2 ]
Cai, Weiquan [3 ]
Wen, Zhenhai [4 ]
Jia, Baohua [5 ]
Wang, Lei [1 ]
Jin, Wei [2 ]
Ma, Tianyi [5 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, State Key Lab Base Ecochem Engn, 53 Zhengzhou Rd, Qingdao 266042, Peoples R China
[2] Tongji Univ, Sch Environm Sci & Engn, State Key Lab Pollut Control & Resources Reuse, 1239 Siping Rd, Shanghai 200092, Peoples R China
[3] Guangzhou Univ, Sch Chem & Chem Engn, 230 Guangzhou Univ City Outer Ring Rd, Guangzhou 510006, Peoples R China
[4] Chinese Acad Sci, Fujian Inst Res Struct Matter, CAS Key Lab Design & Assembly Funct Nanostruct, Fujian Prov Key Lab Nanomat, Fuzhou 350002, Fujian, Peoples R China
[5] Swinburne Univ Technol, Fac Sci Engn & Technol, Ctr Translat Atomat, John St, Hawthorn, Vic 3122, Australia
基金
中国国家自然科学基金;
关键词
aerogels; bismuth; formic acid; tin;
D O I
10.1002/anie.202102832
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical reduction of CO2 (CO2RR) into valuable hydrocarbons is appealing in alleviating the excessive CO2 level. We present the very first utilization of metallic bismuth-tin (Bi-Sn) aerogel for CO2RR with selective HCOOH production. A non-precious bimetallic aerogel of Bi-Sn is readily prepared at ambient temperature, which exhibits 3D morphology with interconnected channels, abundant interfaces and a hydrophilic surface. Superior to Bi and Sn, the Bi-Sn aerogel exposes more active sites and it has favorable mass transfer properties, which endow it with a high FEHCOOH of 93.9 %. Moreover, the Bi-Sn aerogel achieves a FEHCOOH of ca. 90 % that was maintained for 10 h in a flow battery. In situ ATR-FTIR measurements confirmed that the formation of *HCOO is the rate-determining step toward formic acid generation. DFT demonstrated the coexistence of Bi and Sn optimized the energy barrier for the production of HCOOH, thereby improving the catalytic activity.
引用
收藏
页码:12554 / 12559
页数:6
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