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
化学
离子
物理化学
光电子学
有机化学
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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