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镍簇加速分级硫化锌铟纳米花实现前所未有的可见光制氢。

Nickel clusters accelerating hierarchical zinc indium sulfide nanoflowers for unprecedented visible-light hydrogen production.

作者信息

Chen Jun, Wu Si-Jia, Cui Wen-Jun, Guo Yin-Hao, Wang Ting-Wei, Yao Zhi-Wei, Shi Yan, Zhao Heng, Liu Jing, Hu Zhi-Yi, Li Yu

机构信息

School of Petrochemical Engineering, Liaoning Petrochemical University, 1 West Dandong Road, 113001 Fushun, Liaoning, China; State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, 122 Luoshi Road, 430070 Wuhan, Hubei, China.

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, Wuhan University of Technology, 122 Luoshi Road, 430070 Wuhan, Hubei, China.

出版信息

J Colloid Interface Sci. 2022 Feb 15;608(Pt 1):504-512. doi: 10.1016/j.jcis.2021.09.156. Epub 2021 Sep 29.

Abstract

As a typical two-dimensional (2D) metal chalcogenides and visible-light responsive semiconductor, zinc indium sulfide (ZnInS) has attracted much attention in photocatalysis. However, the high recombination rate of photogenerated electrons and holes seriously limits its performance for hydrogen production. In this work, we report in-situ photodeposition of Ni clusters in hierarchical ZnInS nanoflowers (Ni/ZnInS) to achieve unprecedented photocatalytic hydrogen production. The Ni clusters not only provide plenty of active sites for reactions as evidenced by in-situ photoluminescence measurement, but also effectively accelerate the separation and migration of the photogenerated electrons and holes in ZnInS. Consequently, the Ni/ZnInS composites exhibit good stability and reusability with highly enhanced visible-light hydrogen production. In particular, the best Ni/ZnInS photocatalyst exhibits an unprecedented hydrogen production rate of 22.2 mmol·h·g, 10.6 times that of the pure ZnInS (2.1 mmol·h·g). And its apparent quantum yield (AQY) is as high as 56.14% under 450 nm monochromatic light. Our work here suggests that depositing non-precious Ni clusters in ZnInS is quite promising for the potential practical photocatalysis in solar energy conversion.

摘要

作为一种典型的二维(2D)金属硫族化合物和可见光响应半导体,硫化锌铟(ZnInS)在光催化领域备受关注。然而,光生电子和空穴的高复合率严重限制了其产氢性能。在这项工作中,我们报道了在分级结构的ZnInS纳米花(Ni/ZnInS)中原位光沉积镍簇以实现前所未有的光催化产氢。镍簇不仅如原位光致发光测量所证明的那样为反应提供了大量活性位点,而且还有效地加速了ZnInS中光生电子和空穴的分离与迁移。因此,Ni/ZnInS复合材料表现出良好的稳定性和可重复使用性,可见光产氢能力得到显著增强。特别是,最佳的Ni/ZnInS光催化剂展现出前所未有的22.2 mmol·h·g的产氢速率,是纯ZnInS(2.1 mmol·h·g)的10.6倍。并且其在450 nm单色光下的表观量子产率(AQY)高达56.14%。我们在此的工作表明,在ZnInS中沉积非贵金属镍簇对于太阳能转换中潜在的实际光催化应用颇具前景。

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