Tao Lihong, Zhao Jianjun, Chen Jun, Ou Caixia, Lv Weixia, Zhong Shengwen
School of Materials Science and Engineering, Jiangxi Provincial Key Laboratory of Power Batteries and Materials, Jiangxi University of Sciences and Technology Ganzhou 341000 China
Nanoscale Adv. 2021 Mar 27;3(11):3199-3215. doi: 10.1039/d1na00115a. eCollection 2021 Jun 1.
For solving the problems of high solubility in electrolytes, poor conductivity and low active site utilization of organic electrode materials, in this work, 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTCDA) grafted nickel phthalocyanine (TNTCDA-NiPc) was synthesized and used as an anode material for lithium ion batteries. As a result, the dispersibility, conductivity and dissolution stability are improved, which is conducive to enhancing the performance of batteries. The initial discharge capacity of the TNTCDA-NiPc electrode is 859.8 mA h g at 2 A g current density, which is much higher than that of the NTCDA electrode (247.4 mA h g). After 379 cycles, the discharge capacity of the TNTCDA-NiPc electrode is 1162.9 mA h g, and the capacity retention rate is 135.3%, which is 7 times that of the NTCDA electrode. After NTCDA is grafted to the phthalocyanine macrocyclic system, the dissolution of the NTCDA in the electrolyte is reduced, and the conductivity and dispersion of the NTCDA and phthalocyanine ring are also improved, so that more active sites of super lithium intercalation from NTCDA and phthalocyanine rings are exposed, which results in better electrochemical performance. The strategy of grafting small molecular active compounds into macrocyclic conjugated systems used in this work can provide new ideas for the development of high performance organic electrode materials.
为解决有机电极材料在电解质中溶解度高、导电性差和活性位点利用率低的问题,在本工作中,合成了1,4,5,8-萘四甲酸二酐(NTCDA)接枝的镍酞菁(TNTCDA-NiPc)并将其用作锂离子电池的负极材料。结果,其分散性、导电性和溶解稳定性得到改善,这有利于提高电池性能。TNTCDA-NiPc电极在2 A g电流密度下的首次放电容量为859.8 mA h g,远高于NTCDA电极(247.4 mA h g)。经过379次循环后,TNTCDA-NiPc电极的放电容量为1162.9 mA h g,容量保持率为135.3%,是NTCDA电极的7倍。NTCDA接枝到酞菁大环体系后,NTCDA在电解质中的溶解减少,NTCDA与酞菁环的导电性和分散性也得到改善,从而使更多来自NTCDA和酞菁环进行超锂嵌入的活性位点暴露出来,导致更好的电化学性能。本工作中采用的将小分子活性化合物接枝到大环共轭体系中的策略可为高性能有机电极材料的开发提供新思路。