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Construction of defective Mo_(15)S_(19)/CdS-diethylenetriamine heterosctructure photocatalyst for highly active and stable noble-metal-free photocatalytic hydrogen production

机译:具有缺陷的Mo_(15)S_(19)/ CdS-二亚乙基三胺杂结构光催化剂的构建用于高活性和稳定的无贵金属光催化制氢

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摘要

CdS, as semiconductor catalyst, has attracted much attention in photocatalytic production of hydrogen for the wide range utilization of visible light. Usually, noble metal deposited as a co-catalyst on CdS surface is required to achieve high photocatalytic activity. Thus, replacing noble metal via cheap and easy synthesis co-catalyst would be of great value for developing cost-effective photocatalyst. In this work, noble-metal-free defective Mo15S19 combined with CdS-diethylenetriamine (DETA) hybrid makes efficient separation of photoinduced carriers, and more importantly, reduced overpotential for hydrogen evolution reaction, thereby improved catalytic hydrogen evolution performance of designed composite. In particular, 3%Mo15S19/CdS-DETA systems exhibited a high rate of hydrogen production, reaching 3.61 mmol g(-1)h(-1), which is similar with 3%Pt/CdS-DETA and 9.5 and 2.19 times as high as that of CdS nanoparticles (NPs) and CdS-DETA, respectively. At the same time, photocorrosion resistance of 3%Mo15S19/CdS-DETA systems was dramatically improved. According to DFT theoretical calculations, it was found that the enhanced photocatalytic performance and anticorrosion are mainly due to efficient transfer of photoexcited electrons from CdS-DETA to Mo15S19.
机译:CdS作为半导体催化剂,在光催化氢生产中得到了广泛的关注,以广泛利用可见光。通常,为了获得高的光催化活性,需要在CdS表面上沉积作为辅助催化剂的贵金属。因此,通过廉价和容易的合成助催化剂替代贵金属对于开发具有成本效益的光催化剂将具有巨大的价值。在这项工作中,不含贵金属的有缺陷的Mo15S19与CdS-二亚乙基三胺(DETA)杂化物的结合可有效分离光诱导载流子,更重要的是,减少了氢释放反应的过电位,从而提高了设计复合材料的催化氢释放性能。特别是3%Mo15S19 / CdS-DETA系统显示出高的氢气产生率,达到3.61 mmol g(-1)h(-1),与3%Pt / CdS-DETA相似,是9.5和2.19倍分别与CdS纳米颗粒(NPs)和CdS-DETA高。同时,3%Mo15S19 / CdS-DETA系统的耐光蚀性得到了显着提高。根据DFT理论计算,发现增强的光催化性能和耐腐蚀性能主要归因于光激发电子从CdS-DETA到Mo15S19的有效转移。

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