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将高度分散的ZnCdS纳米颗粒锚定在镍钴普鲁士蓝类似物衍生的立方状NiCoP上,形成S型异质结以改善析氢性能。

Anchoring highly-dispersed ZnCdS nanoparticles on NiCo Prussian blue Analogue-derived cubic-like NiCoP forms an S-scheme heterojunction for improved hydrogen evolution.

作者信息

Wang Kai, Xie Haiyan, Li Youji, Wang Guorong, Jin Zhiliang

机构信息

School of Chemistry and Chemical Engineering, Ningxia Key Laboratory of Solar Chemical Conversion Technology, Key Laboratory for Chemical Engineering and Technology, State Ethnic Affairs Commission, North Minzu University, Yinchuan 750021, PRChina.

College of Chemistry and Chemical Engineering, Jishou University, Jishou, Hunan 416000, PR China.

出版信息

J Colloid Interface Sci. 2022 Dec 15;628(Pt B):64-78. doi: 10.1016/j.jcis.2022.08.001. Epub 2022 Aug 3.

DOI:10.1016/j.jcis.2022.08.001
PMID:35985064
Abstract

This study used a facile hydrothermal technique to obtain a novel ZnCdS/NiCoP S-scheme heterojunction for highly photocatalytic H generation, Notably, phosphatization was used to derive the cubic NiCoP from a Prussian blue analog ZnCdS nanoparticles are simple to disperse on the surface because NiCoP has a cubic characteristic, which easily transfers interface charges, and consequently accelerates surface reaction kinetics. Furthermore, the ZnCdS/NiCoP-3% composite exhibited the highest photocatalytic H generation performance of 582.98 µmol with an apparent quantum yield (AQY) of 7.93% at 450 nm in the lactic acid aqueous solution, which is approximately 4.16 and 500-fold higher than that of the pure ZnCdS and NiCoP, respectively. Additionally, outstanding photostability was achieved after 20h of the four cycling experiments. Consequently, the peachy photocatalytic hydrogen evolution can be imputed for establishing S-scheme heterojunction, maintaining doughty redox capacity and achieving spatial separation of charges, thereby vastly restraining the fast recombination of photoexcitation. Furthermore, the photoluminescence (PL) spectroscopy and hydroxyl radical (OH) capture experiments further proved the S-scheme mechanism. Therefore, this study provides a neoteric perspective establishing S-scheme photocatalytic systems for solar energy conversion.

摘要

本研究采用简便的水热技术制备了一种新型的用于高效光催化产氢的ZnCdS/NiCoP S型异质结。值得注意的是,通过磷化作用从普鲁士蓝类似物衍生出立方相NiCoP,ZnCdS纳米颗粒易于分散在其表面,因为NiCoP具有立方相特征,这有利于界面电荷转移,从而加速表面反应动力学。此外,ZnCdS/NiCoP-3%复合材料在乳酸水溶液中表现出最高的光催化产氢性能,在450 nm处的表观量子产率(AQY)为7.93%,产氢量为582.98 μmol,分别约为纯ZnCdS和NiCoP的4.16倍和500倍。此外,在四个循环实验进行20小时后,该复合材料表现出出色的光稳定性。因此,优异的光催化析氢性能可归因于建立了S型异质结、保持了强大的氧化还原能力以及实现了电荷的空间分离,从而极大地抑制了光激发的快速复合。此外,光致发光(PL)光谱和羟基自由基(OH)捕获实验进一步证明了S型机制。因此,本研究为建立用于太阳能转换的S型光催化系统提供了一个新的视角。

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