催化作用
离子键合
可见光谱
光催化
价(化学)
解吸
选择性
吸附
材料科学
光化学
电子转移
化学
离子
物理化学
光电子学
有机化学
生物化学
作者
Wenjie He,Yuechang Wei,Jing Xiong,Zhiling Tang,Yingli Wang,Xiong Wang,Hui Xu,Xiao Zhang,Xiaolin Yu,Zhen Zhao,Jian Liu
标识
DOI:10.1016/j.jechem.2023.01.028
摘要
Herein, the catalysts of ultrathin g-C3N4 surface-modified hollow spherical Bi2MoO6 (g-C3N4/Bi2MoO6, abbreviated as CN/BMO) were fabricated by the co-solvothermal method. The variable valence Mo5+/Mo6+ ionic bridge in CN/BMO catalysts can boost the rapid transfer of photogenerated electrons from Bi2MoO6 to g-C3N4. And the synergy effect of g-C3N4 and Bi2MoO6 components remarkably enhance CO2 adsorption capability. CN/BMO-2 catalyst has the best performances for visible light-driven CO2 reduction compared with single Bi2MoO6 and g-C3N4, i.e., its amount and selectivity of CO product are 139.50 μmol g−1 and 96.88% for 9 h, respectively. Based on the results of characterizations and density functional theory calculation, the photocatalytic mechanism for CO2 reduction is proposed. The high-efficient separation efficiency of photogenerated electron-hole pairs, induced by variable valence Mo5+/Mo6+ ionic bridge, can boost the rate-limiting steps (COOH*-to-CO* and CO* desorption) of selective visible light-driven CO2 conversion into CO. It inspires the establishment of efficient photocatalysts for CO2 conversion.
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