Construction of carbon dots modified hollow g-C3N4 spheres via in situ calcination of cyanamide and glucose for highly enhanced visible light photocatalytic hydrogen evolution

被引:35
|
作者
Ding, Yuan [1 ]
Lin, Zhi [1 ]
Deng, Jiawei [1 ]
Liu, Yingliang [1 ]
Zhang, Li [1 ]
Wang, Kunlun [1 ]
Xu, Shengang [1 ]
Cao, Shaokui [1 ]
机构
[1] Zhengzhou Univ, Sch Mat Sci & Engn, Henan Key Lab Adv Nylon Mat & Applicat, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; Carbon dots; Hollow spheres; In situ calcination; Photocatalyst; Hydrogen evolution; ONE-STEP SYNTHESIS; H-2; EVOLUTION; QUANTUM DOTS; HYDROTHERMAL SYNTHESIS; DOPED G-C3N4; NITRIDE; NANOSHEETS; PERFORMANCE; FABRICATION; PHOTODEGRADATION;
D O I
10.1016/j.ijhydene.2021.10.108
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
In this work, a series of carbon dots (CDs) modified hollow g-C3N4 spheres (HCNS-Cx) were constructed via a double in situ approach using cyanamide and glucose as precursors, respectively. As HCNS-Cx was synthesized by one-step in situ thermal polymerization of two precursors, which could make CDs and g-C3N4 keep tight connection and increase the separation of the photogenerated electron-hole pairs. The average diameter and wall thickness of the HCNS-Cx are about 355 nm and 55 nm, respectively. Under the visible light irradiation, the H-2 evolution rate (HER) of HCNS-C1.0 (2322 mmol g(-1) h(-1)) was 19 times that of bulk g-C3N4 (122 mmol g(-1) h(-1)) and 1.8 times that of HCNS without CDs modification (1289 mmol g-1 h(-1)), respectively. And its apparent quantum efficiency is 17.93% at 420 nm. The specific surface area, light absorption capacity, and charge carrier mobility of HCNS-Cx could be dramatically improved due to the introduction of CDs and hollow structures of g-C3N4 spheres, resulting in a significant improvement of photocatalytic activity. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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页码:1568 / 1578
页数:11
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