多硫化物
催化作用
硫黄
阴极
动力学
化学工程
锂(药物)
化学
材料科学
碘化物
纳米技术
图层(电子)
化学动力学
接口(物质)
储能
反应机理
锂硫电池
活化能
无机化学
高能
作者
Yi Zhang,Xiaosheng Song,Yong Zhao,Geon-Tae Park,Yang-Kook Sun
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-02-10
卷期号:11 (3): 2924-2934
被引量:1
标识
DOI:10.1021/acsenergylett.5c04332
摘要
Quasi-solid-state-polymer-electrolyte-based (QSSE-based) quasi-solid-state lithium–sulfur batteries (QSSLSBs) are an emerging research focus because they are safe and deliver high energy density. However, sluggish interfacial reaction kinetics involving the sulfur cathode and QSSE remains a core developmental bottleneck. Herein, we reveal that the cations and anions of tetrabutylammonium iodide (TBAI) promote S 3 •– generation via a synergistic electrostatic–nucleophilic catalysis mechanism that accelerates lithium polysulfide conversion. Accordingly, we innovatively introduced TBAI into the cathode–QSSE interface to construct an QSSE with a catalytically active interfacial layer that realized enhanced interface reaction kinetics. The cycling performance of the assembled QSSLSBs: an average decay rate of only 0.038% per cycle over 1600 stable long cycles at 0.2 C; a capacity retention of 70.5% after 100 cycles at 0.1 C under a high sulfur loading of 6.5 mg·cm –2 . The synergistic electrostatic–nucleophilic catalysis strategy developed herein provides innovative insight that addresses the sluggish interfacial kinetics of the QSSLSB cathode.
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