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A facile synthesis of Br-modified g-C3N4 semiconductors for photoredox water splitting
被引:463
|作者:
Lan, Zhi-An
[1
]
Zhang, Guigang
[1
]
Wang, Xinchen
[1
]
机构:
[1] Fuzhou Univ, Coll Chem, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Photocatalysis;
Water splitting;
Bromine;
Graphitic carbon nitride;
Doping;
CARBON NITRIDE SEMICONDUCTORS;
HYDROGEN-EVOLUTION;
IN-SITU;
POLYMERS;
PHOTOCATALYSTS;
ENHANCEMENT;
NANOSTRUCTURE;
COCATALYST;
NANOSHEETS;
CATALYSIS;
D O I:
10.1016/j.apcatb.2016.03.062
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:
Hydrogen production by semiconductor photocatalysis using abundant sunlight and water is an ideal method to address the globe energy and environment issues. Here, we present a facile synthesis of bromine doped graphitic carbon nitride (g-C3N4) photocatalysts for hydrogen evolution with visible light irradiation. Bromine modification is shown to enhance the optical, conductive and photocatalytic properties of g-C3N4, while still keeping the poly-tri-s(triazine) core structure as the main building blocks of the materials. This modification method can be generally applicable to several precursors of g-C3N4, including urea, dicyandiamide, ammonium thiocyanide, and thiourea. The optimal sample CNU-Br-0.1 shows more than two times higher H-2 evolution rates than pure CNU sample under visible light irradiation, with high stability during the prolonged photocatalytic operation. Results also found that the photocatalytic O-2 evolution activity of CNU-Br-0.1 was promoted when the sample was subjected to surface kinetic promotion by loading with cobalt oxide as a cocatalyst. This study affords us a feasible modification pathway to rationally design and synthesize g-C3N4 based photocatalysts for a variety of advanced applications, including CO2 photofixation, organic photosynthesis and environmental remediation. (C) 2016 Elsevier B.V. All rights reserved.
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页码:116 / 125
页数:10
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