格式化
异质结
法拉第效率
析氧
电化学
无定形固体
电解
催化作用
材料科学
化学工程
电催化剂
原位
相(物质)
电极
无机化学
化学
结晶学
物理化学
光电子学
有机化学
工程类
电解质
作者
Liang Yu,Wei Zhou,Yanmei Shi,Cuibo Liu,Bin Zhang
标识
DOI:10.1016/j.scib.2020.04.022
摘要
Uncovering the structure evolution and real active species of energy catalytic materials under reaction conditions is important for both understanding structure-activity relationship and constructing electrocatalysts for CO2 electroreduction (CO2ER). And integrating CO2ER with an anodic organic transformation to replace the oxygen evolution reaction is highly desirable. Here, In2O3 is selected as the model material to reveal the surface reconstruction under CO2ER condition. In situ and ex situ results reveal that the electrochemical in situ reconstruction of crystalline In2O3 leads to the formation of crystalline-In/amorphous-In2O3-x heterostructure (In/In2O3-x). In/In2O3-x acts as the real active phase with Faradaic efficiency of ~ 89.2% for the formate, outperforming In (~67.5%). The improved performance can be ascribed to electron-rich In rectified by Schottky effect of In/In2O3-x heterostructure. Impressively, formate and high-value octanenitrile can be simultaneously achieved by integrating CO2ER with octylamine oxidation in an In/In2O3-x‖Ni2P two-electrode electrolyzer.
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