光催化
材料科学
产量(工程)
选择性
光电流
傅里叶变换红外光谱
光化学
化学工程
催化作用
光电子学
化学
有机化学
工程类
冶金
作者
Mengpei Jiang,Chen Li,Keke Huang,Ying Wang,Jinghai Liu,Zhibin Geng,Xiangyan Hou,Jingyu Shi,Shouhua Feng
标识
DOI:10.1021/acsami.0c11072
摘要
As a multiple proton-coupled electron transfer process, photocatalytic conversion of CO 2 usually produces a wide variety of products. Improving the yield and selectivity of CO 2 to the single product is still a significant challenge. In this work, we describe that the rationally constructed W 18 O 49 /Cu 2 O{111} interfaces achieve highly selective CO 2 photocatalytic conversion to CH 4 . In situ Fourier transform infrared spectroscopy measurements reveal that the formation of W 18 O 49 /Cu 2 O{111} interfaces restrains the desorption of CO* intermediates in CO 2 photocatalytic conversion. UPS spectra, PL spectra, and photocurrent curves show that more photogenerated electrons are excited and transferred to W 18 O 49 /Cu 2 O{111} interfaces. All of these play critical roles in CH 4 production. As an outcome, the yield rate of CO 2 photocatalytic conversion to CH 4 was enhanced from 6.5 to 17.20 μmol g –1 h –1 with selectivity as high as 94.7%. The work demonstrates the feasibility and versatility of interface engineering in achieving highly selective CO 2 photocatalytic conversion.
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