材料科学
轨道能级差
阴极
锌
密度泛函理论
电化学
有机自由基电池
席夫碱
电池(电)
化学工程
分子轨道
分子
电极
化学物理
物理化学
计算化学
有机化学
化学
高分子化学
热力学
物理
冶金
工程类
功率(物理)
作者
Zhuolin Ye,Si‐Jun Xie,Ziyi Cao,Lipeng Wang,Dongxiao Xu,Hong Zhang,John Matz,Pei Dong,Huayi Fang,Jianfeng Shen,Mingxin Ye
标识
DOI:10.1016/j.ensm.2021.02.022
摘要
Despite the development of quinone as the potential cathode material for Zn-organic batteries, there are undesired behaviors for the rate and cycling performances. To achieve high-performance Zn-organic batteries, intentional organic molecular design and a deep understanding of the mechanism of Zn-organic batteries are highly essential. Herein, strong electron-withdrawing and conjugating groups (-CN) were introduced to lower the highest occupied molecular orbital (HOMO)/lowest unoccupied molecular orbital (LUMO) energy on an aromatic Schiff base (Hexaazatrinnphthalene, denoted as HATN). With such a decoration, HATN-3CN exhibits an outstanding rate capacity with retention of 60.7% of the initial capacity at 400 times the initial current density and long cycle life of over 5800 cycles. Besides, the charge storage mechanism was systematically investigated through experiments and density functional theory calculation, showing that CN moieties are the active site for the storage of H+/Zn2+. This strategy and insight provided by molecular orbital theory and kinetics-controlled process offer a feasible pathway of molecular-level design for constructing high-performance Zn-organic batteries.
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