Trinitroaromatic Salts as High-Energy-Density Organic Cathode Materials for Li-Ion Batteries

被引:3
作者
Wang, Yaning [1 ,2 ]
Zhao, Xiaolin [2 ,3 ]
Wang, Youwei [2 ,3 ]
Qiu, Wujie [2 ,3 ]
Song, Erhong [2 ,3 ]
Wang, Sufan [1 ]
Liu, Jianjun [2 ,3 ,4 ]
机构
[1] Anhui Normal Univ, Sch Chem & Mat Sci, Wuhu Anhui 241002, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine, Shanghai 200050, Peoples R China
[3] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[4] Univ Chinese Acad Sci, Sch Chem & Mat Sci, Hangzhou Inst Adv Study, Hangzhou 310024, Peoples R China
基金
中国国家自然科学基金;
关键词
donors and acceptors; conjugate effect; chemical structure; charge transfer; redox reactions; ELECTRODE; POLYMER;
D O I
10.1021/acsami.2c18433
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Even though organic molecules with designed structures can be assembled into high-capacity electrode materials, only limited functional groups such as -C=O and -C=N-could be designed as high-voltage cathode materials with enough high capacity. Here, we propose a common chemical raw material, trinitroaromatic salt, to have promising potential to develop organic cathode materials with high discharge voltage and capacity through a strong delocalization effect between -NO2 and aromatic ring. Our first-principles calculations show that electrochemical reactions of trinitroaromatic potassium salt C6H2(NO2)(3)OK are a 6-electron charge-transfer process, providing a high discharge capacity of 606 mAh g(-1) and two voltage plateaus of 2.40 and 1.97 V. Electronic structure analysis indicates that the discharge process from C6H2(NO2)(3)OK to C6H2(NO2Li2)(3)OK stabilizes oxidized [C-6](n+) to achieve a stable conjugated structure through electron delocalization from -NO2 to [C-6](n+). The ordered layer structure C6H2(NO2)(3)OK can provide large spatial pore channels for Li-ion transport, achieving a high ion diffusion coefficient of 3.41 x 10(-6) cm(2) s(-1).
引用
收藏
页码:1129 / 1137
页数:9
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