光催化
材料科学
异质结
选择性
化学工程
吸附
氧气
纳米技术
光化学
催化作用
光电子学
化学
有机化学
工程类
作者
Rongjie Li,Qingjie Luan,Dong Cheng,Wenjun Dong,W.Z. Tang,Ge Wang,Yunfeng Lu
标识
DOI:10.1016/j.apcatb.2020.119832
摘要
Developing well-designed photocatalysts with optimal activity and selectivity is a promising strategy for converting CO2 to renewable fuels. Herein, a self-optimized photocatalyst TiO2@BiOCl is prepared by facile growth of ultrathin BiOCl lamina on the defective surface of TiO2 nanotube. Facilitated from light irradiation, H-incorporated oxygen vacancies form on defective TiO2 nanotube matrix to extend light adsorption range, meanwhile Bi0 atom is reduced from BiOCl lamina to restructure atomic heterojunction BiOCl-Bi0-TiO2. Bi0 atom pours photo-generated electrons directly to Ti3+ in H-incorporated oxygen vacancy, gathering electrons efficiently to accelerate the photocatalytic efficiency. Bi-Ti dual metal sites and H-incorporated oxygen vacancies optimize CO2 reduction path to achieve high CH4 selectivity. Finally, the magnificent surface-reconstruction on TiO2@BiOCl chalks up highest CH4 productivity rate of 168.5 μmol g−1 h−1 and optimal CH4 selectivity of 99.4 % during CO2 photoreduction. Thus, the pioneering construction of efficient photocatalyst with self-optimized strategy paves a new way to fabricate efficient photocatalyst.
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