格式化
X射线光电子能谱
电催化剂
可逆氢电极
甲酸
傅里叶变换红外光谱
电化学
材料科学
氧化还原
无机化学
拉曼光谱
化学工程
电极
化学
催化作用
物理化学
工作电极
工程类
有机化学
光学
物理
作者
Yuta Takaoka,Jun Tae Song,Atsushi Takagaki,Motonori Watanabe,Tatsumi Ishihara
标识
DOI:10.1016/j.apcatb.2023.122400
摘要
In the CO2 electrocatalytic reduction reaction (CO2RR) technology, high CO2 conversion rate is highly required for efficient CO2 utilization from the CO2 resource. In this study, we propose the strategy of combining UiO-66 metal organic framework (MOF) structure with Bi electrocatalyst for highly active CO2RR with selective formic acid production. The synthesized Bi/UiO-66 catalyst shows superior CO2 reduction property, 4.6 times higher current density at −0.7 V vs. reversible hydrogen electrode (RHE) than bare Bi without UiO-66 despite of low electrochemical surface area. Also, NH2 functionalized UiO-66 shows almost no effect on CO2RR as compared to without NH2 probably due to disassembled linkers during CO2RR. Various characterizations such as Fourier transform infrared (FTIR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) indicate carbonate species captured form of CO2 at Zr-MOF site should contribute the high CO2 conversion rate. Our findings demonstrate the feasibility of Zr-MOF as a Supporting material to achieve efficient CO2 reduction.
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