阴极
锂(药物)
化学
离解(化学)
离子
二硫键
电子
电子转移
键离解能
降级(电信)
化学工程
材料科学
化学物理
光化学
物理化学
有机化学
计算机科学
电信
医学
生物化学
物理
量子力学
工程类
内分泌学
作者
Hansong Xing,Wenlong Guo,Shuai Tang,Yubing Si,Jiahan Song,Yongzhu Fu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2023-07-24
卷期号:62 (37): e202308561-e202308561
被引量:17
标识
DOI:10.1002/anie.202308561
摘要
Abstract Organosulfides are promising candidates as cathode materials for the development of electric vehicles and energy storage systems due to their low‐cost and high capacity properties. However, they generally suffer from slow kinetics because of the large rearrangement of S−S bonds and structural degradation upon cycling in batteries. In this paper, we reveal that soluble bis(2‐pyrimidyl) disulfide (Pym 2 S 2 ) can be a high‐rate cathode material for rechargeable lithium batteries. Benefiting from the superdelocalization of pyrimidyl group, the extra electrons prefer to be localized on the π* (pyrimidyl group) than σ* (S−S bond) molecular orbitals initially, generating the anion‐like intermedia of [Pym 2 S 2 ] 2− and thus decreasing the dissociation energy of the S−S bond. It makes the intrinsic energy barrier of dissociative electron transfer depleted, therefore the lithium half cell exhibits 2000 cycles at 5 C. This study provides a distinct pathway for the design of high‐rate, long‐cycle‐life organic cathode materials.
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