Dilution of the Electron Density in the π-Conjugated Skeleton of Organic Cathode Materials Improves the Discharge Voltage

被引:39
作者
Dai, Gaole [1 ]
Gao, Yehua [1 ]
Niu, Zhihui [3 ]
He, Ping [2 ]
Zhang, Xiaohong [1 ]
Zhao, Yu [1 ]
Zhou, Haoshen [2 ,4 ]
机构
[1] Soochow Univ, Jiangsu Key Lab Carbon Based Funct Mat, Inst Funct Nano & Soft Mat FUNSOM, 199 Renai Rd, Suzhou 215123, Jiangsu, Peoples R China
[2] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Coll Engn & Appl Sci, Ctr Energy Storage Mat & Technol, Nanjing 210093, Jiangsu, Peoples R China
[3] Shandong Univ Technol, Sch Phys & Optoelect Engn, Zibo 250049, Shandong, Peoples R China
[4] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058568, Japan
基金
中国国家自然科学基金;
关键词
aromaticity; electron delocalization; high voltage; indolocarbazole; organic batteries; MOLECULAR-ORBITAL METHODS; OVERCHARGE PERFORMANCE; BASIS-SETS; LITHIUM; BATTERY; DESIGN;
D O I
10.1002/cssc.201903502
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organic compounds are promising candidates as battery materials because they can be sourced from sustainable resources, have tunable structures, and are cheap. However, the working voltage of battery cells containing organic compounds as positive electrodes is relatively lower than that of those containing an inorganic counterpart. In this work, a strategy was developed to increase the discharge voltage of battery cells by diluting the electron density of N-based redox centers in conjugated organic materials. In electron-rich heterocyclic compounds that utilize N as the redox center, pentatomic rings such as carbazole derivatives exhibited a higher atomic-dipole-moment-corrected Hirshfeld charge population compared with hexatomic rings, which led to a significant increase in the oxidation potential. As a result, polymeric indolocarbazole derivatives showed a high discharge voltage of 3.7-4.3 V vs. Li+/Li and good cycling performance. Such a strategy can be used to design high-voltage organic electrode materials containing other redox centers.
引用
收藏
页码:2264 / 2270
页数:7
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