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采用铟基金属有机框架前驱体制备的用于光催化析氢且无需助催化剂的硫化锌铟异质结。

ZnInS Heterojunctions Constructed with In-MOF Precursor for Photocatalytic Hydrogen Evolution without Cocatalysts.

作者信息

Zang Shaohong, Cai Xiaorong, Zang Yixian, Jing Fei, Lu Youwei, Tang Shuting, Lin Feng, Mo Liuye

机构信息

Donghai Laboratory, Zhoushan 316021, China.

Institute of Innovation & Application, National Engineering Research Center For Marine Aquaculture, Zhejiang Ocean University, Zhoushan, Zhejiang Province 316022, China.

出版信息

Inorg Chem. 2024 Apr 8;63(14):6546-6554. doi: 10.1021/acs.inorgchem.4c00645. Epub 2024 Mar 27.

DOI:10.1021/acs.inorgchem.4c00645
PMID:38535616
Abstract

ZnlnS has great prospects for photocatalytic water splitting to hydrogen by visible light. Herein, a novel ZnlnS-In-MOF (ZnInS) photocatalyst is elaborately synthesized by in situ method with In-MOF as the template and In as the source. ZnInS overcomes the fast interface charge recombination and a sluggish charge lifetime via the formed heterojunctions. Photoelectrochemical measurements reveal that the charge-transfer kinetics is enhanced since In-MOF is introduced to act as a reliable charge-transport channel. ZnInS exhibits outstanding cocatalyst-free H evolution rate of 70 μmol h under irradiation (λ > 420 nm), which is 3.2-fold higher than that of ZnlnS. In addition, the ZnInS photocatalyst shows good stability in the 16 h continuous reaction. This work illustrates the feasibility of the MOF precursor instead of inorganic salts to directly synthesize photocatalysts with high performance.

摘要

ZnlnS在可见光光催化水分解制氢方面具有广阔前景。在此,以In-MOF为模板、In为源,通过原位法精心合成了一种新型的ZnlnS-In-MOF(ZnInS)光催化剂。ZnInS通过形成的异质结克服了快速的界面电荷复合和缓慢的电荷寿命。光电化学测量表明,由于引入In-MOF作为可靠的电荷传输通道,电荷转移动力学得到增强。ZnInS在光照(λ>420 nm)下表现出70 μmol h的出色无共催化剂析氢速率,比ZnlnS高3.2倍。此外,ZnInS光催化剂在16小时的连续反应中表现出良好的稳定性。这项工作说明了使用MOF前驱体代替无机盐直接合成高性能光催化剂的可行性。

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