In situ growing Cu2(OH)2CO3 on oxidized carbon nitride with enhanced photocatalytic hydrogen evolution and pollutant degradation

被引:13
作者
Chen, Dan [1 ]
Wang, Xiaonan [1 ]
Zhang, Xiaoqiao [2 ]
Wang, Weide [3 ]
Xu, Yao [1 ]
Zhang, Yingying [1 ]
Qian, Guangren [1 ]
机构
[1] Shanghai Univ, Sch Environm & Chem Engn, 99 Shangda Rd, Shanghai 200444, Peoples R China
[2] SINOPEC, Res Inst Petr Proc, 18 Xue Yuan Rd, Beijing 100083, Peoples R China
[3] Shandong Ind Tech Sch, Dept Marine Biochem, 6789 West Ring Rd, Weifang 261053, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxidized carbon nitride; Cu-2(OH)(2)CO3; Photocatalyst; Hydrogen evolution; Degradation of malachite green; FACILE FABRICATION; H-2; EVOLUTION; EFFICIENT; NANOSHEETS; WATER; G-C3N4; PERFORMANCE; COCATALYST; MORPHOLOGY; CONVERSION;
D O I
10.1016/j.ijhydene.2020.06.225
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
A novel composite has been successfully synthesized in situ via a coprecipitation method about the coupling of Cu-2(OH)(2)CO3 with oxidized carbon nitride (O-g-C3N4) forming Cu-2(OH)(2)CO3/O-g-C3N4 (CuCN) heterojunction structure. The as-prepared composites were characterized by diverse means. The CuCN composite with 3:5 mass ratio of Cu-2(OH)(2)CO3 to O-g-C3N4 (60CuCN) presented an extremely excellent photocatalytic activity. The photocatalytic H-2 evolution of 60CuCN was around 23.26 and 44.62 times higher than that of g-C3N4 and Cu-2(OH)(2)CO3, respectively. The photocatalytic degradation malachite green (MG) rate of 60CuCN was up to 91%, which was around 2.2 and 4.8 times as much as that of g-C3N4 and Cu-2(OH)(2)CO3, respectively. These results are mainly attributed to the structure property of O-g-C3N4 and the heterojunction structure of the composite, which could effectively accelerate the separation and transfer rate of photogenerated electrons and holes. The holes (h(+)) and superoxide radicals (center dot O-2(-)) played a dominant role in photocatalytic degradation MG reaction. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:24697 / 24709
页数:13
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