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通过硫化镍纳米片修饰的中空硫化锌镉纳米球的可控制备用于高效光催化产氢

Controlled preparation of hollow ZnCdS nanospheres modified by NiS nanosheets for superior photocatalytic hydrogen production.

作者信息

Lu Lili, Ma Yongjin, Liu Hongqin, Dong Rui, Tan Pengfei, Yang Lu, Pan Jun

机构信息

State Key Laboratory for Powder Metallurgy, Central South University, Changsha 410083, PR China.

Hunan Provincial Collaborative Innovation Center for Environment and Energy Photocatalysis, Changsha University, Changsha 410083, PR China.

出版信息

J Colloid Interface Sci. 2022 Jan 15;606(Pt 1):1-9. doi: 10.1016/j.jcis.2021.08.006. Epub 2021 Aug 4.

Abstract

Developing durable and efficient photocatalysts for H evolution is highly desirable to expedite current research on solar-chemical energy conversion. In this work, a novel photocatalytic H evolution system based on ZnCdS/NiS nanocomposite was rationally designed for the first time. In this advanced composite structure, NiS nanosheets as a co-catalyst were intimately coupled to the inner surface of the hollow spherical ZnCdS. The construction of the hollow spherical shell shortened the distance of charge migration to the surface site and increased the multiple absorption of incident light. The introduction of NiS nanosheets increased the light absorption capacity of the composite system and also greatly improved the separation and migration behavior of photo-generated carriers due to its narrower band gap and relatively low conduction band position, which had been confirmed by DRS, EIS and PL. As a result, the hollow ZnCdS/NiS composite material exhibited excellent photocatalytic activity. At the loading amount of NiS up to 15 at.%, the hollow ZnCdS/NiS composite exhibited the best photocatalytic activity with a corresponding H production rate of 22.637 mmol gh, which was 1.42 times and 1.85 times that of hollow ZnCdS and solid ZnCdS, respectively. Moreover, this novel catalyst also displayed a long-term stability without apparent debasement in H evolution activity. It is expected that this work could provide new inspiration to the design and development of other highly active photocatalytic systems for water splitting.

摘要

开发耐用且高效的用于析氢的光催化剂对于加速当前太阳能-化学能转换的研究非常必要。在这项工作中,首次合理设计了一种基于ZnCdS/NiS纳米复合材料的新型光催化析氢系统。在这种先进的复合结构中,作为助催化剂的NiS纳米片紧密地耦合到空心球形ZnCdS的内表面。空心球壳的构建缩短了电荷迁移到表面位点的距离,并增加了对入射光的多次吸收。NiS纳米片的引入提高了复合系统的光吸收能力,并且由于其较窄的带隙和相对较低的导带位置,也极大地改善了光生载流子的分离和迁移行为,这已通过漫反射光谱(DRS)、电化学阻抗谱(EIS)和光致发光(PL)得到证实。结果,空心ZnCdS/NiS复合材料表现出优异的光催化活性。在NiS的负载量高达15原子%时,空心ZnCdS/NiS复合材料表现出最佳的光催化活性,相应的析氢速率为22.637 mmol g⁻¹ h⁻¹分别是空心ZnCdS和实心ZnCdS的1.42倍和1.85倍。此外,这种新型催化剂还表现出长期稳定性,析氢活性没有明显降低。预计这项工作可以为设计和开发其他用于水分解的高活性光催化系统提供新的灵感。

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