异质结
光催化
吸附
选择性
解吸
化学工程
密度泛函理论
产量(工程)
材料科学
多孔性
降级(电信)
化学
光化学
催化作用
纳米技术
光电子学
物理化学
有机化学
计算化学
复合材料
计算机科学
工程类
电信
作者
Jiale He,Jie Lin,Zheng Xu,Yingfei Hu,Qingling Huang,Guobing Zhou,Wei Li,Jianqiang Hu,Na Hu,Zhen Yang
标识
DOI:10.1016/j.cej.2023.148036
摘要
Developing highly-selective and efficient photocatalysts for converting CO2 into carbon-based fuels by solar energy is desirable, whereas it is still a severe challenge. Herein, we present a unique interfacial Mo-S bond-bridged hierarchical S-scheme heterostructured photocatalysts, prepared by in-situ loading ZnIn2S4 nanoflakes (ZIS-NFs) on the Bi2MoO6 porous micro-spheres (BMO-PMs) assembled from numerous nanosheets. The interfacial Mo-S bonds can reinforce the separation and migration of photoinduced charge carriers via the S-scheme mechanism in the BMO@ZIS heterostructure. Besides, its hierarchical heterostructure can improve the visible-light response ability, and afford plenty of active sites so as to benefit the CO2 adsorption and activation. Specifically, the combined results of experiment and density functional theory (DFT) calculations indicate that the fine heterostructure can not only convert the endoergic rate-determining step of bare ZIS (namely, CO2* hydrogenation to form COOH*) to an exoergic reaction process and lower the overall activation energy barrier, but also boost the desorption of CO* from the ZIS surface. As a result, in existence of H2O vapor without any sacrificial agents, the optimum photocatalyst ([email protected]) manifests the outstanding CO2 photoreduction activity, with a CO yield and selectivity of 23.11 μmol g−1h−1 and 93.1 %, respectively, higher than those of the most reported photocatalysts. This work offers an in-depth insight for fabricating the interfacial chemical bond-modulated hierarchical S-scheme heterostructure with a remarkable performance of CO2 conversion.
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