"Dyed" graphitic carbon nitride with greatly extended visible-light-responsive range for hydrogen evolution

被引:64
作者
Fang, Jiawen [1 ,2 ]
Fan, Huiqing [1 ,3 ]
Zhu, Ziye [1 ]
Kong, Ling Bing [2 ]
Ma, Longtao [1 ]
机构
[1] Northwestern Polytech Univ, Sch Mat Sci & Engn, State Key Lab Solidificat Proc, Xian 710072, Peoples R China
[2] Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore
[3] China Acad Engn Phys, Natl Key Lab Shock Wave & Detonat Phys, 64 Mianshan Rd, Mianyang 621900, Peoples R China
关键词
Graphitic carbon nitride; Dye; Methyl orange; Broad spectral responsive range; Hydrogen evolution; PHOTOCATALYTIC ACTIVITY; SEMICONDUCTORS; NANOSHEETS; WATER; POLYMERIZATION; ABSORPTION; CATALYSTS; UREA;
D O I
10.1016/j.jcat.2016.03.021
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
The precursor of carbon nitride pretreated with dye sensitization (methyl orange) before condensation would possess a spectral response of the resultant product extended even to the near-infrared range. The color of the products, in this case, can be delicately controlled by the amount and kind of dyes, so the process is termed "dyeing." Their corresponding absorption edge would reach 560 and 675 nm after introduction of 0.05 and 0.15 g dye, respectively. It is assumed that the chromophores and auxochromes that impart color to the molecules are introduced into the pi-conjugated system and also extend delocalization. The highest hydrogen evolution rate of the dyed carbon nitride reached 470 mu mol/g h, compared with an increase by a factor of 1.7 for bulk carbon nitride. This new concept of dyeing will inspire further investigation on developing broad spectral light-responsive photocatalysts for hydrogen production. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:93 / 101
页数:9
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