详细信息

Rationally designed Ta3N5@ReS2 heterojunctions for promoted photocatalytic hydrogen production  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Rationally designed Ta3N5@ReS2 heterojunctions for promoted photocatalytic hydrogen production

作者:Zhan, Xiaoqiang[1,2];Fang, Zhi[2];Li, Bing[1];Zhang, Haitao[2];Xu, Leyao[2];Hou, Huilin[2];Yang, Weiyou[2]

机构:[1]East China Univ Sci & Technol, Sch Mech & Power Engn, Shanghai 200237, Peoples R China;[2]Ningbo Univ Technol, Inst Micro Nano Mat & Devices, Ningbo 315211, Peoples R China

年份:2021

卷号:9

期号:47

起止页码:27084

外文期刊名:JOURNAL OF MATERIALS CHEMISTRY A

收录:;EI(收录号:20215111354984);WOS:【SCI-EXPANDED(收录号:WOS:000723282000001)】;

基金:This work was supported by a project funded by the National Natural Science Foundation of China (NSFC, Grant No. 51972178, 52074130 and 51774145), China Postdoctoral Science Foundation (Grant No. 2020M681966), the exchange project of the sixth China-Northern Macedonia Science and Technology Meeting (Grant No. 6-11) and Natural Science Foundation of Ningbo Municipal Government (Grant No. 202003N4164 and 2021J145).

语种:英文

外文关键词:Charge transfer - Hydrogen production - Heterojunctions - Rhenium compounds - Nitrogen compounds

摘要:Highly-active heterojunctions hold the pivotal function in photocatalytic hydrogen evolution reaction (HER). Herein, Ta3N5@ReS2 photocatalysts are rationally designed via the combination of template-assisted, hydrothermal and solution-adsorption processes, in which few-layered ReS2 nanosheets are anchored on hollow Ta3N5 nanospheres with intimate contact for charge transfer. The photocatalytic H-2 production rate of Ta3N5@ReS2 heterojunctions reaches 739.4 mu mol g(-1) h(-1), which is similar to 16 times higher than that of the bulk Ta3N5 counterpart, and superior to those of Ta3N5-based photocatalysts ever reported. According to the experimental results and theory calculation, it is proposed that such designed Ta3N5@ReS2 heterojunctions could be highly effective for enhancing the absorptivity of light, improving charge separation and transfer, as well as increasing edge active sites for HER, thus leading to the promoted H-2-evolution kinetics.

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