4.8 Article

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

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 22, 页码 12554-12559

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202102832

关键词

aerogels; bismuth; formic acid; tin

资金

  1. National Natural Science Foundation of China [22002068, 51772162, 52072197]
  2. Youth Innovation and Technology Foundation of Shandong Higher Education Institutions, China [2019KJC004]
  3. Outstanding Youth Foundation of Shandong Province, China [ZR2019JQ14]
  4. Taishan Scholar Young Talent Program [tsqn201909114]
  5. Major Scientific and Technological Innovation Project [2019JZZY020405]
  6. Natural Science Foundation of Shandong Province [ZR2020ZD09]
  7. Natural Science Foundation of Shandong Province of China [ZR2019BB002, ZR2018BB031]
  8. Tongji Hundred Talents Program
  9. Fundamental Research Funds for the Central Universities

向作者/读者索取更多资源

The study introduced the use of a metallic bismuth-tin aerogel for electrochemical reduction of CO2 with selective formic acid production, demonstrating high FEHCOOH and stability. Experimental and theoretical findings confirmed that the coexistence of bismuth and tin optimized the energy barrier for formic acid generation, enhancing catalytic activity.
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.

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