光催化
降级(电信)
制氢
氢
化学
光化学
芘
化学工程
材料科学
化学物理
有机化学
催化作用
电信
计算机科学
工程类
作者
Xiaorong Cai,Yixian Zang,Shaohong Zang,Shuting Tang,Fei Jing,Liuye Mo,Dehong Teng,Wei Lin,Guigang Zhang
标识
DOI:10.1016/j.apsusc.2023.157871
摘要
Recently, Step-scheme (S-scheme) photocatalysts possess great prospects because of the unique charge transport route and high efficiency of charge separation in photocatalysis. Herein, binary Znln2S4/pyrene-benzene polymer (ZIS-PyP) S-scheme heterojunction was fabricated by an in-situ method. The resulting ZIS-PyP exhibits an excellent photocatalytic H2 evolution rate of 54 μmol h−1 which is 2.5 and 10.8-fold than pure ZnIn2S4 and PyP, respectively. The trapping agent experiments reveal the main active species are ·O2− and h+ in the TCH degradation reaction. The characteristic experiments and DFT calculations were used to elucidate the photocatalytic mechanism. The average hydrogen adsorption free energy of ZIS-PyP-H is determined to be −1.51 eV, smallest than that of ZIS-H and PyP-H, which indicates the most favorable for hydrogen mass transfer in ZIS-PyP. Driven by band bending, built-in electric field and Coulombic repulsion, a unique electronic transmission along S-scheme route between ZnIn2S4 and PyP was formed. Therefore, the powerful electrons left in the LUMO of PyP and strong holes in VB of ZnIn2S4 attended to reactions, ultimately achieved an optimal hydrogen production and TCH degradation efficiency in ZIS-PyP S-scheme system.
科研通智能强力驱动
Strongly Powered by AbleSci AI