化学
电化学
格式化
法拉第效率
催化作用
双金属片
可逆氢电极
锡
选择性
电极
纳米颗粒
化学工程
无机化学
纳米技术
物理化学
工作电极
材料科学
有机化学
工程类
作者
Qing Li,Jiaju Fu,Wenlei Zhu,Zhengzheng Chen,Bo Shen,Liheng Wu,Zheng Xi,Tanyuan Wang,Gang Lü,Jun‐Jie Zhu,Shouheng Sun
摘要
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.
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