Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/118052
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorSchool of Fashion and Textiles-
dc.contributorResearch Institute for Intelligent Wearable Systems-
dc.contributorResearch Institute for Smart Energy-
dc.contributorMainland Development Office-
dc.creatorZhou, J-
dc.creatorLuo, Y-
dc.creatorWang, C-
dc.creatorXie, C-
dc.creatorWang, H-
dc.creatorGuo, Y-
dc.creatorYang, Y-
dc.creatorLi, Z-
dc.creatorWen, S-
dc.creatorCai, J-
dc.creatorHuang, Q-
dc.creatorZheng, Z-
dc.date.accessioned2026-03-12T01:03:20Z-
dc.date.available2026-03-12T01:03:20Z-
dc.identifier.urihttp://hdl.handle.net/10397/118052-
dc.language.isoenen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_US
dc.rights© 2026 The Author(s). EcoMat published by The Hong Kong Polytechnic University and John Wiley & Sons Australia, Ltd.en_US
dc.rightsThe following publication J. Zhou, Y. Luo, C. Wang, et al., “A LiFSI-Based Ultralight Electrolyte for Long-Cycle-Life and High-Energy-Density Lithium-Sulfur Batteries,” EcoMat8, no. 2 (2026): e70050 is available at https://doi.org/10.1002/eom2.70050.en_US
dc.subjectHigh energy densityen_US
dc.subjectLiFSIen_US
dc.subjectLithium-sulfur batteriesen_US
dc.subjectLong cycle lifeen_US
dc.subjectUltralight electrolytesen_US
dc.titleA LiFSI-based ultralight electrolyte for long-cycle-life and high-energy-density lithium-sulfur batteriesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume8-
dc.identifier.issue2-
dc.identifier.doi10.1002/eom2.70050-
dcterms.abstractLithium-sulfur (Li-S) batteries are promising candidates for high-energy storage; however, the high electrolyte uptake of porous S cathodes significantly limits their practical energy density. Although ultralight electrolytes (ULEs) can address this issue, they often suffer from low ionic conductivity, unstable interphases, and sluggish kinetics. This study presents a ULE design based on lithium bis(fluorosulfonyl)imide (LiFSI) salt, which simultaneously achieves a low density (0.89 g cm−3) and high Li+ conductivity (7.05 mS cm−1). The LiFSI salt facilitates the formation of a LiF-rich solid electrolyte interphase on the Li metal anode, effectively suppressing polysulfide corrosion and enhancing cycle life. Furthermore, its high donor number improves polysulfide solubility, accelerating conversion kinetics and increasing capacity utilization. As a result, high-loading S cathodes (5 mg cm−2) deliver an initial capacity of 1180 mAh g−1 and retain 70.63% of this capacity after 200 cycles. Pouch cells with the LiFSI-ULE exhibit a 34.5% higher energy density and a 133% longer cycle life compared to those with conventional electrolytes. This study successfully extends the application of LiFSI to Li-S batteries, offering a viable pathway toward long-cycling, high-energy-density energy storage.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationEcoMat, Feb. 2026, v. 8, no. 2, e70050-
dcterms.isPartOfEcoMat-
dcterms.issued2026-02-
dc.identifier.scopus2-s2.0-105028940760-
dc.identifier.eissn2567-3173-
dc.identifier.artne70050-
dc.description.validate202603 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TAen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe authors acknowledge the financial support from Guangdong Hong Kong Technology Cooperation Funding Scheme (GHP/047/20GD), National Natural Science Foundation of China/Hong Kong Research Grants Council (CRS_PolyU504/22), Research Grants Council (R5019-22), National Natural Science Foundation of China (52203318, 52401268), and the Hong Kong Polytechnic University (1-W22M, 1-BDYU). This work was supported by National Natural Science Foundation of China (Grants 52203318 and 52401268), Guangdong Hong Kong Technology Cooperation Funding Scheme (Grant GHP/047/20GD), Hong Kong Polytechnic University (Grants 1-BDYU and 1-W22M), Research Grants Council (Grant R5019-22) and National Natural Science Foundation of China/Hong Kong Research Grants Council (Grant CRS_PolyU504/22).en_US
dc.description.pubStatusPublisheden_US
dc.description.TAWiley (2026)en_US
dc.description.oaCategoryTAen_US
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