阳极
材料科学
电化学
聚合物
酞菁
锂(药物)
化学工程
多孔性
电流密度
高分子化学
无机化学
纳米技术
化学
电极
物理化学
复合材料
内分泌学
工程类
物理
医学
量子力学
作者
Lihua Guo,Chunhua Li,Yougui Zhou,Xinmeng Hao,Huipeng Li,Hong Shang,Bing Sun
出处
期刊:Dalton Transactions
[Royal Society of Chemistry]
日期:2023-01-01
卷期号:52 (38): 13745-13749
被引量:6
摘要
Porous organic polymers (POPs) are a novel class of polymeric materials with high flexibility and designability for building structures. Herein, a phthalocyanine-based porous organic polymer (PcPOP) was constructed in situ on copper foil from H2Pc(ethynyl)4 [Pc(ethynyl)4 = 2(3),9(10),16(17),23(24)-tetra(ethynyl)phthalocyanine] by the coupling reaction. Benefiting from the uniformly distributed electron-rich nitrogen atoms in the Pc structure and the sp-hybridized carbons in the acetylenic linkage, Li intercalation in the porous organic polymer would be improved and stabilized. As a result, PcPOP showed remarkable electrochemical performance in lithium-ion batteries as the anode, including high specific capacity (a charge capacity of 1172 mA h g-1 at a current density of 150 mA g-1) and long cycling stability (a reversible capacity of 960.1 mA h g-1 can be achieved even after 600 cycles at a current density of 1500 mA g-1). The result indicates that the intrinsic doping of electron-rich sites of the building molecules is beneficial for the electrochemical performance of the porous organic polymer.
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