双功能
格式化
拉曼光谱
材料科学
碳纳米纤维
氧化锡
二氧化锡
锡
氧化物
吸附
化学工程
金属
纳米纤维
无机化学
纳米技术
催化作用
化学
物理化学
有机化学
光学
冶金
工程类
物理
作者
Junjie Chen,Benhua Ma,Zhoubing Xie,Weimo Li,Yumei Yang,Ming Mu,Xiaoxin Zou,Bing Zhao,Wei Song
标识
DOI:10.1016/j.apcatb.2022.122350
摘要
Monitoring the reaction intermediates and revealing the real active sites are of great importance for elucidation mechanism and designing ideal catalysts. Here, bifunctional porous SnO2/Ag nanofibers (P-SnO2/Ag) are prepared and present high Faradaic efficiency (FE) of 92.4% for formate with a current density of 24.6 mA cm−2 at − 0.9 V (vs. RHE). The in-situ SERS spectra reveal that tin-oxide in P-SnO2/Ag nanofibers are easy reduced, indicates metallic tin likely be the real active site rather than Sn (IV) and Sn (II) oxide species in CO2RR. The characteristic SERS peak at around 1420 cm−1 corresponding to the key *OCHO* intermediate for HCOO- production is also captured, favorably formed after the first *CO2- intermediate suitably adsorbed on P-SnO2/Ag nanofibers via oxygen atoms. Combining the intrinsic SERS properties and excellent catalytic performance of P-SnO2/Ag nanofibers, a real correlation is established between the composition and chemical structure of the materials and their catalytic performance.
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