多硫化物
氧化还原
动力学
硫黄
电解质
锂(药物)
半反应
无机化学
化学
化学工程
有机化学
电极
医学
物理化学
物理
量子力学
工程类
内分泌学
作者
Meng Zhao,Bo‐Quan Li,Xiang Chen,Jin Xie,Hong Yuan,Jia‐Qi Huang
出处
期刊:Chem
[Elsevier]
日期:2020-10-13
卷期号:6 (12): 3297-3311
被引量:203
标识
DOI:10.1016/j.chempr.2020.09.015
摘要
Lithium-sulfur (Li–S) battery affords an ultrahigh theoretical energy density of 2,600 Wh kg−1 as a promising next-generation energy storage technique, whose actual performance is heavily dependent on the sulfur redox kinetics. Lithium polysulfide intermediates play a decisive role on the complex sulfur redox reactions but are unfortunately insufficient to afford rapid kinetics, rendering reduced specific capacity especially at high rates. Herein, a redox comediation strategy is proposed and an organopolysulfide (di-t-butyl disulfide, DtbDS) is introduced as a model comediator to accelerate the sulfur redox kinetics. Concretely, DtbDS reacts with lithium polysulfides and provides a kinetically favorable pathway for polysulfide conversion. Consequently, high-rate (4 C), high-sulfur-loading (5 mg cm−2), or lean-electrolyte (5.0 μL mgS−1) Li–S batteries are realized. The redox comediation strategy demonstrates a novel approach to promote the sulfur redox kinetics for high-performance Li–S batteries and inspires more redox comediators represented by DtbDS.
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