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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Photocatalytic hydrogen generation on bifunctional ternary heterostructured In2S3/MoS2/CdS composites with high activity and stability under visible light irradiation
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Photocatalytic hydrogen generation on bifunctional ternary heterostructured In2S3/MoS2/CdS composites with high activity and stability under visible light irradiation

机译:双功能三元异质结构In2S3 / MoS2 / CdS复合材料在可见光照射下具有高活性和稳定性的光催化制氢

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摘要

A bifunctional ternary heterostructured In2S3/MoS2/CdS composite photocatalyst with high activity and stability under visible light irradiation was fabricated via a simple hydrothermal method. The bifunctional ternary heterostructured photocatalyst displayed higher activity for photocatalytic hydrogen evolution than GO/CdS and rGO/CdS composites and can be compared with the hydrogen-gennerating efficiency of systems containing the well-known Pt co-catalyst. But above all, the photocorrosion of CdS was also suppressed effectively. The heterojunction structure between MoS2 and CdS promoted the interfacial charge transfer process, suppressed the charge recombination and enhanced the performance of photocatalytic hydrogen generation. Due to the well matching of the VB of CdS with that of In2S3, holes on the VB of CdS could be easily transferred to that of In2S3 via the heterojunction structure between In2S3 and CdS, which prevented the accumulation of holes on the VB of CdS, inhibited its photocorrosion and dramatically enhanced its stability. The structure sequence and deposition site play an important role in photocatalytic activity: MoS2 deposited on the interface of CdS and In2S3 was more efficient in promoting charge transfer and thus significantly improved the photocatalytic activity of the composite photocatalyst. Our findings pave a way to design bifunctional CdS-based ternary heterostructured composites for highly efficient H-2 generation and photocorrosion suppression.
机译:通过简单的水热法制备了在可见光照射下具有高活性和稳定性的双功能三元异质结构In2S3 / MoS2 / CdS复合光催化剂。该双功能三元异质结构光催化剂显示出比GO / CdS和rGO / CdS复合材料更高的光催化氢释放活性,并且可以与包含众所周知的Pt助催化剂的系统的氢产生效率进行比较。但最重要的是,CdS的光腐蚀也得到了有效抑制。 MoS2和CdS之间的异质结结构促进了界面电荷转移过程,抑制了电荷复合并增强了光催化制氢的性能。由于CdS的VB与In2S3的VB很好地匹配,CdS的VB上的空穴可以通过In2S3和CdS之间的异质结结构轻松转移到In2S3的空穴上,从而防止了空穴在CdS的VB上的积累,抑制其光腐蚀并显着增强其稳定性。结构顺序和沉积位点在光催化活性中起着重要作用:沉积在CdS和In2S3界面上的MoS2在促进电荷转移方面更为有效,因此显着提高了复合光催化剂的光催化活性。我们的发现为设计基于双功能CdS的三元异质结构复合材料铺平了道路,该复合材料可高效产生H-2和抑制光腐蚀。

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