| Literature DB >> 28291338 |
Qing Li1,2, Jiaju Fu2,3, Wenlei Zhu2, Zhengzheng Chen4, Bo Shen2, Liheng Wu2, Zheng Xi2, Tanyuan Wang1, Gang Lu4, Jun-Jie Zhu3, Shouheng Sun2.
Abstract
Tin (Sn) is known to be a good catalyst for electrochemical reduction of CO2 to formate in 0.5 M KHCO3. But when a thin layer of SnO2 is coated over Cu nanoparticles, the reduction becomes Sn-thickness dependent: the thicker (1.8 nm) shell shows Sn-like activity to generate formate whereas the thinner (0.8 nm) shell is selective to the formation of CO with the conversion Faradaic efficiency (FE) reaching 93% at -0.7 V (vs reversible hydrogen electrode (RHE)). Theoretical calculations suggest that the 0.8 nm SnO2 shell likely alloys with trace of Cu, causing the SnO2 lattice to be uniaxially compressed and favors the production of CO over formate. The report demonstrates a new strategy to tune NP catalyst selectivity for the electrochemical reduction of CO2 via the tunable core/shell structure.Entities:
Year: 2017 PMID: 28291338 DOI: 10.1021/jacs.7b00261
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419