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Two-dimensional nickel hydroxide/sulfides nanosheet as an efficient cocatalyst for photocatalytic H2 evolution over CdS nanospheres.

Authors :
Xie, Ying Peng
Zheng, Yunhui
Yang, Yongqiang
Jiang, Renzheng
Wang, Guosheng
Zhang, Yajing
Zhang, Enlei
Zhao, Liang
Duan, Chun-Ying
Source :
Journal of Colloid & Interface Science. Mar2018, Vol. 514, p634-641. 8p.
Publication Year :
2018

Abstract

The intriguing features of two-dimensional (2D) materials such as better charge carrier separation and abundant surface reaction sites endow them with potential applications as cocatalysts in photocatalysis. In this paper, a ternary 2D nickel hydroxide/sulfides nanosheet composed of Ni(OH) 2 , Ni 3 S 2 and Ni x S 6 was loaded on CdS nanospheres by a simple chemical deposition route. The composition of nickel hydroxide/sulfides was determined clearly through an overall analysis using X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy. Mott-Schottky, electrochemical impedance, steady-state and time-resolved photoluminescence spectroscopy were used to investigate the charge transfer process in CdS and Ni(OH) 2 /Ni 3 S 2 /Ni x S 6 -CdS. The results confirm that a synergistic effect of Ni(OH) 2 /Ni 3 S 2 /Ni x S 6 on CdS has occurred under light irradiation, where the Ni(OH) 2 and nickel sulfides act as hole storage and surface reaction sites, respectively, to promote the charge transfer on CdS. The improved charge transfer and separation efficiency as well as the increased surface reaction sites in Ni(OH) 2 /Ni 3 S 2 /Ni x S 6 -CdS finally result in a dramatically improved photocatalytic performance. The photocatalytic H 2 evolution rate of Ni(OH) 2 /Ni 3 S 2 /Ni x S 6 -CdS is ca . 46 times higher than that of CdS, and the photocatalytic stability of CdS is also improved substantially under visible light irradiation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
514
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
127760589
Full Text :
https://doi.org/10.1016/j.jcis.2017.12.080