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Synergetic effect of copper species as cocatalyst on LaFeO3 for enhanced visible-light photocatalytic hydrogen evolution
被引:40
|作者:
Li, Juanjuan
[1
,2
]
Pan, Xinwei
[1
]
Xu, Yingrui
[1
]
Jia, Lishan
[1
]
Yi, Xiaodong
[1
]
Fang, Weiping
[1
]
机构:
[1] Xiamen Univ, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
[2] Chinese Acad Sci, Inst Urban Environm, Key Lab Urban Environm & Hlth, Xiamen 361021, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Copper species;
LaFeO3;
catalyst;
Reduction treatment;
Hydrogen production;
Visible-light;
WATER;
TIO2;
PEROVSKITES;
REDUCTION;
NANOCOMPOSITE;
GENERATION;
MORPHOLOGY;
CATALYSTS;
LA2CUO4;
ROLES;
D O I:
10.1016/j.ijhydene.2015.07.166
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:
LaFeO3 has been reported to have excellent optoelectronic properties and a narrow bandgap, which make it a promising candidate for photocatalytic reactions. In this work, to further improve the photocatalytic water-splitting performance by enhancing the separation of photo-excited carriers and providing active sites for H-2 production, cocatalysts (copper species) supported on the perovskite-type oxide LaFeO3 was obtained by a citrate complexation and reduction treatment. Copper ions in the perovskite lattice are easily reduced and LaFeO3 possesses good stability in reducing atmospheres; thus, a series of stable LaFeO3 with a controllable copper species were synthesized and characterized by XRD, DRS, XPS and PL. The results showed that copper species (Cu-0 and Cu+) supported on the LaFeO3 surface brought about a significant enhancement of photocatalytic activity. The LaFe0.8 + LaCu0.2 treated at 300 degrees C exhibited the highest photocatalytic activity, with a H-2 evolution rate of 343 mu mol g(-1) h(-1), which was attributed to the fact that a proper Cu-0 to Cu+ ratio (Cu-0/Cu+ = 1.34) could serve as a cocatalyst for photocatalytic hydrogen evolution, providing accelerated electron hole separation and proton-reduction sites. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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页码:13918 / 13925
页数:8
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