Novel hydrogen bonding composite based on copper phthalocyanine/perylene diimide derivatives p-n heterojunction with improved photocatalytic activity. (February 2017)

• Record Type: Journal Article
• Authors: Wang, Hailong; Zhao, Lele; Liu, Xueqiang; Xu, Jing; Hou, Wenlong; Wang, Jianmin; He, Enfang; Zhang, Ruijun; Zhang, Haiquan
• Is Part Of: Dyes and pigments. Volume 137(2017)
• Page Start: 322
• Page End: 328
• Publication Date: 2017-02
• Subjects: Heterojunction-type photoeatalysts -- Hydrogen bond composites -- Photocatalytic mechanism -- Degradation of rhodamine B -- Copper phthalocyanine/perylene diimide derivatives; Dyes and dyeing -- Periodicals; Pigments -- Periodicals; 667.2
• DOI: 10.1016/j.dyepig.2016.11.014
• Languages: English
• ISSNs: 0143-7208

Abstract

Abstract: 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) was the main reactive species for the degradation of RhB. Graphical abstract: A novel PDIC12/CuTcPc p-n heterojunction-type photoeatalysts for enhancing photocatalytic performance under visible-light irradiation. Highlights: PDIC12/CuTcPc p-n heterostructure is a novel organic composite photocatalyst. PDIC12 greatly promotes the visible light-driven photocatalytic activity of CuTcPc. PDIC12/CuTcPc displays excellent visible light photocatalytic activity (λ > 400 nm). The resulting hydroxyl radical (OH) played the major roles for RhB degradation. Provide useful insights to improve the performance of traditional photocatalysts.