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Dual Functional High Donor Electrolytes for Lithium-Sulfur Batteries under Lithium Nitrate Free and Lean Electrolyte Conditions
Univ Fribourg, Dept Chem, CH-1700 Fribourg, Switzerland..
Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea.;Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South Korea..
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry - BMC, Organic Chemistry.ORCID iD: 0000-0002-8075-1482
Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 08826, South Korea.;Seoul Natl Univ, Inst Chem Proc, Seoul 08826, South Korea..
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2022 (English)In: ACS Energy Letters, E-ISSN 2380-8195, Vol. 7, no 8, p. 2459-2468Article in journal (Refereed) Published
Abstract [en]

Electrolyte engineering is a highly promising strategy in lithium-sulfur batteries to increase the sulfur utilization and maintain a stable interface at the lithium metal anode for long-term cycling. Whereas high donor electrolytes can increase the solubility of polysulfides to promote the sulfur utilization and therefore operate under lean electrolyte conditions, their poor thermodynamic stability toward lithium metal anode causes uncontrolled decomposition at its interface and impair the cycle life severely. Here, we introduce a dual functional high donor electrolyte, 3-fluoropyridine (3-FPN), to simultaneously achieve high polysulfide solubility up to 1.5 M and compatibility with lithium metal. These features result in a high specific capacity of 1087.9 mAh g(sulfur)(-1) and robust cycling under a lean electrolyte condition of 7 mu Lelectrolyte mgsulfur-1in the absence of LiNO3. Remarkably, 3-FPN preserves stable cyclability even at a high areal sulfur loading of 8 mgsulfur cm-2, which opens a new avenue in advancing the electrolytes for lithium-sulfur batteries toward their high volumetric energy density and long cycle life.

Place, publisher, year, edition, pages
American Chemical Society (ACS), 2022. Vol. 7, no 8, p. 2459-2468
National Category
Materials Chemistry Condensed Matter Physics
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URN: urn:nbn:se:uu:diva-482710DOI: 10.1021/acsenergylett.2c00874ISI: 000826965500001Scopus ID: 2-s2.0-85136849153OAI: oai:DiVA.org:uu-482710DiVA, id: diva2:1690688
Available from: 2022-08-26 Created: 2022-08-26 Last updated: 2025-02-20Bibliographically approved

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Sethio, Daniel

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