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硫化镉纳米颗粒在镍金属有机框架纳米片上的边缘取向生长用于光催化析氢

Edge-oriented growth of cadmium sulfide nanoparticles on nickel metal-organic framework nanosheets for photocatalytic hydrogen evolution.

作者信息

Huang Han, Ding Liyong, Wang Xuedong, Jiang Qingqing, Li Qin, Hu Juncheng

机构信息

Hubei Key Laboratory of Catalysis and Materials Science, School of Chemistry and Materials Science, South-Central Minzu University, Wuhan 430074, PR China.

College of Chemical and Material Engineering, Quzhou University, Quzhou 324000, PR China.

出版信息

J Colloid Interface Sci. 2024 Sep 15;670:86-95. doi: 10.1016/j.jcis.2024.05.083. Epub 2024 May 14.

Abstract

In this study, a directional loading of cadmium sulfide (CdS) nanoparticles (NPs) was achieved on the opposite edges of nickel metal-organic framework (Ni-MOF) nanosheets (NSs) by adjusting the weight ratio of CdS NPs in the reaction process to produce effective visible light photocatalysts. The close contact between the zero-dimensional (0D) and two-dimensional (2D) regions and the matching positions of the bands promoted charge separation and heterojunction formation. The optimal CdS NPs loading of composite material was 40 wt%. At this ratio, CdS NPs grew primarily at the opposite edges of the Ni-MOF NSs rather than on their surfaces. When lactic acid was used as the sacrificial agent, the hydrogen production rate of the 40 %-CdS/Ni-MOF heterojunction under visible light irradiation was 19.6 mmol h g, making a 20-fold enhancement compared to the original CdS NPs sample (1.0 mmol h g). The charge carriers generated in CdS NPs were transferred to Ni-MOF NSs through heterojunctions, where Ni-MOF NSs also served as cocatalysts to improve hydrogen production. The combination of the two materials improved the light absorption ability. In particular, the 40 %-CdS/Ni-MOF heterojunction exhibited good photostability, effectively preventing the photocorrosion of CdS NPs. This study introduces an approach for constructing efficient and stable photocatalysts for visible light-driven photocatalytic hydrogen production.

摘要

在本研究中,通过在反应过程中调整硫化镉(CdS)纳米颗粒(NPs)的重量比,在镍金属有机框架(Ni-MOF)纳米片(NSs)的相对边缘实现了硫化镉纳米颗粒的定向负载,从而制备出有效的可见光光催化剂。零维(0D)和二维(2D)区域之间的紧密接触以及能带的匹配位置促进了电荷分离和异质结的形成。复合材料中CdS NPs的最佳负载量为40 wt%。在此比例下,CdS NPs主要生长在Ni-MOF NSs的相对边缘而非其表面。当使用乳酸作为牺牲剂时,40%-CdS/Ni-MOF异质结在可见光照射下的产氢速率为19.6 mmol h g,与原始CdS NPs样品(1.0 mmol h g)相比提高了20倍。CdS NPs中产生的电荷载流子通过异质结转移到Ni-MOF NSs上,其中Ni-MOF NSs也作为助催化剂提高产氢量。两种材料的结合提高了光吸收能力。特别是,40%-CdS/Ni-MOF异质结表现出良好的光稳定性,有效防止了CdS NPs的光腐蚀。本研究介绍了一种构建用于可见光驱动光催化产氢的高效稳定光催化剂的方法。

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