光催化
甲酸
化学
光电流
量子产额
光化学
辐照
二氧化钛
兴奋剂
氧气
可见光谱
核化学
无机化学
催化作用
化学工程
材料科学
有机化学
光电子学
光学
核物理学
工程类
物理
荧光
作者
Pengju Du,Tongming Su,Xuan Luo,Xiantai Zhou,Zuzeng Qin,Hongbing Ji,Jianhua Chen
标识
DOI:10.1002/cjoc.201700761
摘要
Abstract Bi‐ and Y‐codoped TiO 2 photocatalysts were synthesized through a sol‐gel method, and they were applied in the photocatalytic reduction of CO 2 to formic acid under visible light irradiation. The results revealed that, after doping Bi and Y, the surface area of TiO 2 was increased from 5.4 to 93.1 m 2 /g when the mole fractions of doping Bi and Y were 1.0% and 0.5%, respectively, and the lattice structures of the photocatalysts changed and the oxygen vacancies on the surface of the photocatalysts formed, which would act as the electron capture centers and slow down the recombination of photo‐induced electron and hole. The photocurrent spectra also proved that the photocatalysts had better electronic transmission capacities. The HCOOH yield in CO 2 photocatalytic reduction was 747.82 μmol/g cat by using 1% Bi‐0.5% Y‐TiO 2 as a photocatalyst. The HCOOH yield was 1.17 times higher than that by using 1% Bi‐TiO 2 , and 2.23 times higher than that by using pure TiO 2 . Furthermore, the 1% Bi‐0.5% Y‐TiO 2 showed the highest apparent quantum efficiency (AQE) of 4.45%.
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