Poly(dibenzothiophene-S,S-dioxide) with visible light-induced hydrogen evolution rate up to 44.2 mmol h-1 g-1 promoted by K2HPO4

被引:54
作者
Shu, Ge [1 ]
Li, Yuda [1 ]
Wang, Zhuang [1 ]
Jiang, Jia-Xing [2 ]
Wang, Feng [1 ]
机构
[1] Wuhan Inst Technol, Key Lab Green Chem Proc, Minist Educ, Sch Chem Engn & Pharm, Wuhan 430073, Hubei, Peoples R China
[2] Shaanxi Normal Univ, Key Lab Macromol Sci Shaanxi Prov, Xian 710062, Shaanxi, Peoples R China
基金
湖北省教育厅重点项目;
关键词
Conjugated polymers; Photocatalysts; Dibenzothiophene-S; S-dioxide; Phosphorylation; Hydrogen evolution rate; GRAPHITIC CARBON NITRIDE; CONJUGATED MICROPOROUS POLYMERS; PHOTOCATALYTIC H-2 EVOLUTION; ARTIFICIAL PHOTOSYNTHESIS; ORGANIC PHOTOCATALYSTS; METAL-FREE; WATER; NANOSHEETS; SEMICONDUCTORS; FRAMEWORKS;
D O I
10.1016/j.apcatb.2019.118230
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 polymers have recently emerged as encouraging metal-free photocatalysts for solar energy conversion under visible light irradiation. Unfortunately, photocatalytic activities of the current polymers are still inadequate. Herein, we present a simple but quite attractive conjugated homopolymer (PDBTSO) based a dibenzothiophene-S,S-dioxide moiety. The introduction of sulphonyl group to a polyfluorene-like backbone can cause richly available active sites and lead to the efficient separation of photoexcited charge carriers, thus yielding impressive photocatalytic performance. Furthermore, we explored a natural "phosphorylation" strategy for increasing photocatalytic hydrogen production over PDBTSO. Remarkably, an extremely high hydrogen evolution rate of 44.2 mmol h(-1) g(-1) was achieved with the optimum addition of K2HPO4 under visible light irradiation.
引用
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页数:7
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