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
物理
工程类
内分泌学
医学
量子力学
生物化学
作者
Hansong Xing,Wenlong Guo,Shuai Tang,Yubing Si,Jiahan Song,Yongzhu Fu
标识
DOI:10.1002/anie.202308561
摘要
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 (Pym2 S2 ) 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 [Pym2 S2 ]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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