Regulated effect of organic small molecular doped in carbon nitride skeleton for boosting photocatalytic hydrogen evolution

被引:10
|
作者
Zhou, Xiangtong [1 ]
Xu, Baojian [1 ]
Zhang, Juan
Zhao, Qilu
Li, Chunmei [2 ]
Dong, Hongjun [2 ]
Wang, Xinling [3 ]
Yang, Jing [3 ]
机构
[1] Jiangsu Univ, Sch Environm & Safety Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Jiangsu Univ, Inst Green Chem & Chem Technol, Sch Chem & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[3] Henan Univ Chinese Med, Coll Pharm, Zhengzhou 450046, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Carbon nitride; 1-Benzyl-3-phenylthiourea; Doping effect; Photocatalytic hydrogen evolution; Charge separation behavior; G-C3N4; NANOSHEETS; QUANTUM DOTS; EFFICIENT; PERFORMANCE; STRATEGY; 2,4,6-TRIAMINOPYRIMIDINE; ACIDIFICATION; DEGRADATION; NANOTUBES; IRON;
D O I
10.1016/j.ijhydene.2021.09.096
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
Organic small molecules doping in polymer carbon nitride (PCN) skeleton can dramatically improve photocatalytic performance owing to its effective regulation effect on molecular and electronic structure. Here, a new PCN-based photocatalyst is obtained via polymeri-zation of urea with 1-benzyl-3-phenylthiourea (BPT). The doping effect of BPT in PCN skeleton directly adjusts the hybridization states and delocalization of molecular orbitals, so that the visible light harvest ability, adsorption capacity, charge separation efficiency and transfer kinetics are improved significantly. Consequently, the photocatalytic hydrogen evolution reaction (HER) rate reaches to 125.0 mmol h(-1) over the optimal PCN-BPT15 photocatalyst, which is as 13.9 times as PCN (9.0 mmol h(-1)). Noteworthily, a high apparent quantum efficiency (AQE) of 24.2% is achieved at 420 nm for photocatalytic HER. This work enriches the functionalized investigations of PCN-like photocatalysts by insight into regulated effect of organic small molecules in the skeleton for photocatalytic applications. (c) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:38299 / 38309
页数:11
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