Donor-acceptor type triazine-based conjugated porous polymer for visible-light-driven photocatalytic hydrogen evolution

被引:99
|
作者
Yu, Jie [1 ]
Sun, Xiaoqin [1 ]
Xu, Xiaoxiang [1 ,2 ]
Zhang, Chi [1 ]
He, Xiaoming [1 ]
机构
[1] Tongji Univ, Sch Chem Sci & Engn, Shanghai Key Lab Chem Assessment & Sustainabil, 1239 Siping Rd, Shanghai 200092, Peoples R China
[2] Tongji Univ, Putuo Peoples Hosp, Clin & Cent Lab, 1291 Jiangning Rd, Shanghai 200060, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Conjugated microporous polymers; Metal-free synthesis; Photocatalyst; Water splitting; Hydrogen production; COVALENT ORGANIC FRAMEWORK; MICROPOROUS POLYMERS; WATER; DESIGN; EFFICIENT; PERFORMANCE; NANOSHEETS;
D O I
10.1016/j.apcatb.2019.117935
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
Conjugated microporous polymers (CMPs) are an emerging class of promising photocatalysts because of their large specific surface areas and adjustable optical band gaps. To avoid the metal contamination, metal-free synthetic procedure for making CMPs for photocatalytic water splitting are highly desired. Herein, we designed and synthesized two triazine-based conjugated microporous polymers P1 and P2 through a simple, efficient, metal-free catalyzed approach. Through linking donor-acceptor (D-A) type pyrazole-benzothiadiazole-pyrazole light-absorbing units by triazine units, P1 has an ideal optical band gap of about 2.3 eV and exhibits a high H-2 evolution rate (HER) of 50 mu mol h(-1) under visible light illumination (lambda >= 420 nm) and apparent quantum efficiency (AQE) as high as 3.58% at 420 +/- 20 run. In contrast, by replacing electron-neutral benzene instead of electron-withdrawing benzothiadiazole, P2 shows obvious hypochromatic shift in the absorption and large optical band gap of about 2.9 eV, as well as poor photocatalytic property.
引用
收藏
页数:9
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