Novel heteroatom sulfur porphyrin organic polymer as a metal-free electrocatalyst for acidic oxygen reduction reaction

被引:26
|
作者
Yan, Wei [1 ]
Cao, Shoufu [1 ]
Xiao, Zuoxu [1 ]
Dai, Fangna [1 ]
Xing, Tao [2 ]
Li, Zhi [2 ]
Chen, Yanli [1 ]
Lu, Xiaoqing [1 ]
Li, Xiyou [1 ]
机构
[1] China Univ Petr East China, Sch Mat Sci & Engn, Qingdao 266580, Peoples R China
[2] Yankuang Grp CO LTD, Zoucheng 273500, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Porphyrin organic polymer; Metal-free; Acid ORR; Electrocatalysts; CARBON; PHTHALOCYANINE; CATALYSTS; GRAPHENE; CATHODE;
D O I
10.1016/j.electacta.2021.138107
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The rational design of a highly reactive electronic structure as the active sites is crucial for the development of oxygen reduction reaction (ORR) catalysts. Herein, a unique ethynyl-linked sulfur-containing porphyrin organic polymer (S-POP) is firstly developed as a metal-free catalyst for ORR under acidic conditions, which possess intrinsic porous structures and easily accessible active sites for the adsorption of oxygen. The S-POP exhibits a superior ORR performance with onset potential of 0.82 V and half-wave potential of 0.72 V, achieving one of the best results among metal-free polymer-based ORR catalysts in acidic conditions, the high ORR activity of S-POP is attributed to the exposure of active sites under the test environment. In particular, it is discovered that after replacing pyrrole N by S atoms, the remaining aza N in S-POP exhibit higher ORR activity than those in conventional porphyrin organic polymer (POP). Density functional theory calculations shows that the significant improvement of S-POP over POP is from the redistribution and reduction of the density of charges on aza N, which promotes *O desorb process and decreases the overpotential. This work provides a novel guidance towards designing and modifying metal-free ORR electrocatalysts with a clear electronic structure as the active sites. (C) 2021 Published by Elsevier Ltd.
引用
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页数:7
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