High-Energy Quasi-Solid-State Lithium-Sulfur Batteries Based on Electrostatic-Nucleophilic Synergy
- Authors
- Zhang, Yi; Song, Xiaosheng; Zhao, Yong; Park, Geon-Tae; Sun, Yang-Kook
- Issue Date
- Mar-2026
- Publisher
- AMER CHEMICAL SOC
- Citation
- ACS ENERGY LETTERS, v.11, no.3, pp 2924 - 2934
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACS ENERGY LETTERS
- Volume
- 11
- Number
- 3
- Start Page
- 2924
- End Page
- 2934
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/214321
- DOI
- 10.1021/acsenergylett.5c04332
- ISSN
- 2380-8195
- Abstract
- 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 S3 center dot- 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<middle dot>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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