甲酸甲酯
甲醇
拉曼光谱
格式化
催化作用
材料科学
无机化学
电化学
化学工程
抗血小板
钙钛矿(结构)
X射线吸收光谱法
化学
吸收光谱法
氮化物
纳米技术
电极
有机化学
图层(电子)
物理化学
工程类
物理
光学
量子力学
作者
Lei Zhao,Qijiao Sun,Mao Li,Yafei Zhong,Peiqi Shen,Yunxiang Lin,Kun Xu
标识
DOI:10.1007/s40843-022-2311-y
摘要
Perovskite oxides with flexible compositions and electronic structures have great potential for application in electrocatalytic water oxidation reactions. However, few studies have focused on the application of perovskite oxides in electrocatalytic oxidation reactions of organic molecules, probably due to the absence of active species because of the poor conductivity and high energy barrier of the surface reconstruction. Herein, we report Cu3N nanosheets with a typical antiperovskite structure as electrocatalysts for selectively converting methanol to formate. The as-prepared antiperovskite nitride Cu3N samples exhibit a Faradic efficiency exceeding 90% for methanol to formate over a wide potential range, which was further confirmed by online electrochemical mass spectrometry and in situ infrared reflectance absorption spectroscopy. Moreover, the high-resolution transmission electron microscopy, X-ray absorption spectroscopy, and in situ Raman spectroscopy results indicate that the core-shell structure formed by generating surface Cu(II) species triggers the electrocatalytic methanol oxidation reaction activity, whereas the pristine Cu3N core facilitates the electron transport inside the catalyst during the electrocatalytic process. This study provides a modelable scheme for the highly selective conversion of methanol and introduces a novel nonoxide perovskite material for the electrochemical conversion of small-organic molecules.
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