Donor-Acceptor Conjugated Porphyrin-Based Polymer for Excellent Hydrogen Evolution Reaction

被引:4
作者
Gu, Shengshen [1 ]
Lu, Jiacheng [1 ]
Xu, Haimei [2 ]
Wang, Danfeng [1 ]
Marianov, Aleksei N. [3 ]
Xie, Haijiao [4 ]
Zhong, Jing [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[2] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Peoples R China
[3] Macquarie Univ, Macquarie Analyt & Fabricat Facil, Sydney, NSW 2109, Australia
[4] Hangzhou Yanqu Informat Technol Co Ltd, Hangzhou 310003, Peoples R China
关键词
porphyrin; 2D polymer; hydrogen evolution reaction; donor-acceptor pair; electrocatalysis; COVALENT ORGANIC FRAMEWORK; ELECTROCHEMICAL HYDROGEN; OXYGEN EVOLUTION; EFFICIENT; METALLOPORPHYRINS; ELECTROCATALYSTS;
D O I
10.1021/acsapm.3c02916
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A two-dimensional, donor-acceptor (D-A) conjugated polymer CoTEPP has been synthesized via Sonogashira coupling between the acceptor benzothiadiazole and the donor porphyrin. The resulting polymer CoTEPP exhibits good efficiency in catalyzing hydrogen evolution reaction (HER) in aqueous media, and its performance is superior to those of other porphyrin-based polymers in terms of both lower overpotentials and larger catalytic currents. CoTEPP has shown an onset potential of 355 mV for a current density of -10 mA/cm(2) and a Tafel slope of 133 mV/dec. The activity has been retained after 1500-cycle potential scans, confirming the good stability of the catalyst. The catalyst achieved a Faradic efficiency (FE) of 96% for hydrogen over 10 h. The improved performance could be attributed to the donor-acceptor pair in the structure, which facilitates electron transfer, as indicated by density functional theory (DFT) calculations. This work demonstrates an alternative strategy for designing porphyrin-based polymers with enormous potential for HER.
引用
收藏
页码:2686 / 2694
页数:9
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