The pH effects on H2 evolution kinetics for visible light water splitting over the Ru/(CuAg)0.15In0.3Zn1.4S2 photocatalyst

被引:34
作者
Zhang, Guangshan [1 ,2 ]
Zhang, Wen [3 ]
Minakata, Daisuke [5 ]
Chen, Yongsheng [2 ]
Crittenden, John [2 ,4 ]
Wang, Peng [1 ]
机构
[1] Harbin Inst Technol, Sch Municipal & Environm Engn, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
[2] Georgia Inst Technol, Sch Civil & Environm Engn, Atlanta, GA 30332 USA
[3] New Jersey Inst Technol, Dept Civil & Environm Engn, Newark, NJ 07102 USA
[4] Georgia Inst Technol, Brook Byers Inst Sustainable Syst, Atlanta, GA 30332 USA
[5] Michigan Technol Univ, Dept Civil & Environm Engn, Houghton, MI 49931 USA
关键词
Ru/(CuAg)(0.15)In0.3Zn1.4S2; H-2; production; pH effect; Visible light irradiation; Water splitting; SOLID-SOLUTION PHOTOCATALYSTS; HYDROGEN-PRODUCTION; TIO2; NANOPARTICLES; AQUEOUS-SOLUTION; REDOX MEDIATOR; IODINE; NANOSTRUCTURES; GENERATION; SULFIDE; SIZE;
D O I
10.1016/j.ijhydene.2013.06.140
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
Much progress has been made in the development of novel visible light photocatalysts that split water into hydrogen (H-2) and oxygen (O-2). In this study, we examine the impact of initial solution pH on H-2 production using an Ru/(CuAg)(0.15)In0.3Zn1.4S2 photocatalyst under visible light irradiation. In addition, the reaction mechanism was analyzed by examining the oxidation products of the electron donor (I-) at different solution pH values. The results show that the initial pH significantly influenced the rate of H-2 production and quantum yield (QY). In particular, the photocatalyst yielded the highest apparent QY (similar to 12.8%) at 420 +/- 5 nm and highest H-2 production rate (similar to 525 mu mol h(-1)) at pH 2; with increasing pH, the H-2 production and QY decreased significantly. The oxidation product of I- at pH <6 was mainly I-3(-), whereas at pH >6 water splitting did not occur at all, so no IO3- or I-2 were observed. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11727 / 11736
页数:10
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