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author:

Xing Wu (Xing Wu.) [1] | Wang Zhou (Wang Zhou.) [2] | Chao Ye (Chao Ye.) [3] | Jiahao Zhang (Jiahao Zhang.) [4] | Zheyuan Liu (Zheyuan Liu.) [5] | Chengkai Yang (Chengkai Yang.) [6] | Jinfeng Peng (Jinfeng Peng.) [7] | Jilei Liu (Jilei Liu.) [8] | Ping Gao (Ping Gao.) [9]

Abstract:

Organic electrode materials are promising for next‐generation energy storage materials due to their environmental friendliness and sustainable renewability. However, problems such as their high solubility in electrolytes and low intrinsic conductivity have always plagued their further application. Polymerization to form conjugated organic polymers can not only inhibit the dissolution of organic electrodes in the electrolyte, but also enhance the intrinsic conductivity of organic molecules. Herein, we synthesized a new conjugated organic polymer (COPs) COP500‐CuT2TP (poly [5,10,15,20‐tetra(2,2′‐bithiophen‐5‐yl) porphyrinato] copper (II)) by electrochemical polymerization method. Due to the self‐exfoliation behavior, the porphyrin cathode exhibited a reversible discharge capacity of 420 mAh g−1, and a high specific energy of 900 Wh Kg−1 with a first coulombic efficiency of 96 % at 100 mA g−1. Excellent cycling stability up to 8000 cycles without capacity loss was achieved even at a high current density of 5 A g−1. This highly conjugated structure promotes COP500‐CuT2TP combined high energy density, high power density, and good cycling stability, which would open new opportunity for the designable and versatile organic electrodes for electrochemical energy storage.

Keyword:

conjugated organic polymers lithium-ion batteries porphyrin thiophene

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Source :

Angewandte Chemie International Edition

ISSN: 1433-7851

Year: 2024

Issue: 14

Volume: 63

Page: n/a-n/a

1 6 . 1 0 0

JCR@2023

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ESI Highly Cited Papers on the List: 0 Unfold All

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30 Days PV: 2

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