光电阴极
化学
涂层
半导体
光电化学
化学工程
纳米技术
金属
金属有机骨架
化学能
光电化学电池
电化学
电极
光电子学
电解质
材料科学
有机化学
物理化学
吸附
电子
工程类
物理
量子力学
作者
Xi Deng,Rui Li,Shudong Wu,Li Wang,Jiahua Hu,Jun Ma,Wenbin Jiang,Ning Zhang,Xusheng Zheng,Chao Gao,Linjun Wang,Qun Zhang,Junfa Zhu,Yujie Xiong
摘要
Photoelectrochemical (PEC) reduction of CO2 into chemical fuels and chemical building blocks is a promising strategy for addressing the energy and environmental challenges, which relies on the development of p-type photocathodes. Cu2O is such a p-type semiconductor for photocathodes but commonly suffers from detrimental photocorrosion and chemical changes. In this communication, we develop a facile procedure for coating a metal–organic framework (MOF) on the surface of a Cu2O photocathode, which can both prevent photocorrosion and offer active sites for CO2 reduction. As evidenced by ultrafast spectroscopy, the formed interface can effectively promote charge separation and transfer. As a result, both the activity and durability of Cu2O are dramatically enhanced for PEC CO2 reduction. This work provides fresh insights into the design of advanced hybrid photoelectrodes and highlights the important role of interfacial charge dynamics in PEC CO2 conversion.
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