Photochemical preparation of atomically dispersed nickel on cadmium sulfide for superior photocatalytic hydrogen evolution

被引:91
作者
Zhang, Huizhen [1 ]
Dong, Yuming [1 ]
Zhao, Shuang [1 ]
Wang, Guangli [1 ]
Jiang, Pingping [1 ]
Zhong, Jun [2 ]
Zhu, Yongfa [3 ]
机构
[1] Jiangnan Univ, Int Joint Res Ctr Photorespons Mol & Mat, Key Lab Synthet & Biol Colloids, Sch Chem & Mat Engn, Wuxi 214122, Jiangsu, Peoples R China
[2] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Inst Funct Nano & Soft Mat Lab FUNSOM, Suzhou 215123, Peoples R China
[3] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Single-site; Ni; Photocatalyst; Water-splitting; HIGHLY EFFICIENT COCATALYST; IN-SITU PHOTODEPOSITION; SEMICONDUCTOR NANORODS; H-2; EVOLUTION; CARBON; TIO2; NI(OH)(2); CATALYSTS; FACETS; G-C3N4;
D O I
10.1016/j.apcatb.2019.118233
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Up to now, hydrogen production with a low-cost and efficient system driven by sunlight still remains a great challenge. Herein, atomically dispersed Ni modified CdS nanorods (NRs) hybrid photocatalyst (Ni-1/CdS) with Ni loading up to 2.85 wt% was prepared by a facile, rapid and scalable photochemical method. Under optimal conditions, the highest rate for H-2 evolution of Ni-1/CdS photocatalyst is 630.1 mmol g(-1) h(-1) under visible light, which is one of the most robust photocatalytic HER systems based on CdS currently. Furthermore, the Ni-1/CdS catalyst exhibits good stability and durability for hydrogen evolution reaction (HER) and outstanding photo catalytic activity under sunlight and aerobic conditions, indicating the great practical value of present reaction system. Density functional theory (DFT) calculations reveal that the introduction of single Ni atom on the CdS can improve the hydrogen binding energy and electronic properties, thus greatly boosting the photocatalytic H-2 production activity.
引用
收藏
页数:9
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