Haloid acid induced carbon nitride semiconductors for enhanced photocatalytic H2 evolution and reduction of CO2 under visible light

被引:41
|
作者
Wan, Shipeng [1 ,4 ]
Ou, Man [1 ,2 ]
Zhong, Qin [1 ,4 ]
Cai, Wei [3 ,4 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
[3] Nanjing Univ Informat Sci & Technol Nanjing, Sch Environm Sci & Engn, Nanjing 210044, Jiangsu, Peoples R China
[4] Nanjing AIREP Environm Protect Technol Co Ltd, Nanjing 210091, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
HYDROGEN EVOLUTION; CHARGE-TRANSFER; DOPED G-C3N4; NANOSHEETS; WATER; ULTRATHIN; DIOXIDE; FUEL; FABRICATION; COCATALYST;
D O I
10.1016/j.carbon.2018.08.003
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
Hexagonal tubular carbon nitride (CN) was successfully fabricated from hexagonal rod-like supramolecular precursor. The supramolecular precursor was synthesized by hydrogen bonded self-assembly of melamine and cyanuric acid, in which cyanuric acid was from in-situ hydrolysis of melamine under haloid acid-assisted hydrothermal environment. The obtained hexagonal tubular CNs not only possess hierarchical micro-nanostructure, increased specific surface area, together with an enlarged band gap energy of 2.85 +/- 0.05 eV, but also show better light absorption capacity in visible to near-infrared region and improved separation rate of photogenerated carriers. Therefore, they exhibit enhanced photocatalytic reduction performance on water splitting to H-2, the largest hydrogen evolution rate can reach 2948.5 mu mol g(-1) h(-1), which is better than most reported CNs. Simultaneously, they also have excellent photocatalytic reduction ability on the conversion of CO2 to H-2, CO and CH4, exhibiting higher averaged electron consumption than previously reported semiconductor photocatalysts. Finally, the photocatalytic reduction mechanism over the synthetic tubular CN is proposed and discussed. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:465 / 474
页数:10
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