Novel hydrogen bonding composite based on copper phthalocyanine/perylene diimide derivatives p-n heterojunction with improved photocatalytic activity

被引:33
|
作者
Wang, Hailong [1 ]
Zhao, Lele [1 ]
Liu, Xueqiang [2 ]
Xu, Jing [1 ]
Hou, Wenlong [1 ]
Wang, Jianmin [1 ]
He, Enfang [1 ]
Zhang, Ruijun [1 ]
Zhang, Haiquan [1 ]
机构
[1] Yanshan Univ, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Peoples R China
[2] Yanshan Univ, Sch Informat Sci & Engn, Qinhuangdao 066004, Peoples R China
关键词
Heterojunction-type photoeatalysts; Hydrogen bond composites; Photocatalytic mechanism; Degradation of rhodamine B; Copper phthalocyanine/perylene diimide derivatives; VISIBLE-LIGHT PHOTOCATALYST; THIN-FILM; PERYLENE; CARBON; PHOTODEGRADATION; DEGRADATION; HETEROSTRUCTURES; NAPHTHALENE; OXIDATION; WATER;
D O I
10.1016/j.dyepig.2016.11.014
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Among photocatalytic materials, p-n heterojunction-type photocatalysts has good photocatalytic performance under visible light irradiation. Herein, a novel Copper phthalocyanine/perylene diimide derivatives p-n heterojunction photoeatalysts based on the intermolecular hydrogen bond between pyridyl and carboxyl was designed and characterized using FT-IR, UV-vis and photoluminescence spectra, and then compared their photocatalytic performance by degradation for rhodamine B (RhB) under visible light irradiation. The hydrogen bond composites shows significant higher photocatalytic activity comparing with its parent, and the photocatalysis increased with increasing of mole fraction of perylene diimide derivatives. The change of morphology and p-n heterojunction structure are in favor of the high photocatalytic active. Furthermore, the photocatalytic mechanism was investigated by radical scavengers testing, that confirmed hydroxyl radical ((OH)-O-center dot) was the main reactive species for the degradation of RhB. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:322 / 328
页数:7
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