4.8 Article

Sulfur-Rich Polymers Based Cathode with Epoxy/Ally Dual-Sulfur-Fixing Mechanism for High Stability Lithium-Sulfur Battery

期刊

ACS NANO
卷 15, 期 9, 页码 15027-15038

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c05330

关键词

lithium-sulfur batteries; organosulfur polymers; epoxy/allyl compound system; dual-sulfur-fixing mechanism; outstanding cycling stability

资金

  1. Liao Ning Revitalization Talents Program [XLYC1907144]
  2. Dalian Youth Science andTechnology Star Project Support Program [2017RQ104]
  3. National Key Research and Development Program of China [2020YFB0311600]

向作者/读者索取更多资源

The research introduces a novel dual-sulfur-fixing mechanism of epoxy/allyl compound/sulfur system to prepare poly(sulfur-random-4-vinyl-1,2-epoxycyclohexane) (SVE) copolymers as powerful cathode materials for Li-S batteries. The SVE electrodes exhibit stable C-S bonds and uniform distribution of ultrafine Li2S/S-8, reducing polysulfides migration and forming a protective layer for enhanced cycle stability. Optimized SVE electrodes deliver high reversible specific capacity and stable cycling performance over more than 400 cycles, providing an effective strategy for practical application of organosulfur polymers in Li-S batteries.
Lithium-sulfur (Li-S) batteries have attracted a great deal of attention for the next-generation energy storage devices due to their inherently high theoretical energy density, high natural abundance, and low cost. However, the dissolution of polysulfides in electrolytes and their undesirable shuttle behavior lead to poor cycling performance, which obstructs practical application. Herein, we report a dual-sulfur-fixing mechanism of epoxy/allyl compound/sulfur system to prepare poly(sulfur-random-4-vinyl-1,2-epoxycyclohexane) (SVE) co-polymers as powerful cathode materials. Benefiting from the stable C-S bond and a uniform distribution of ultrafine Li2S/S-8 in the SVE-based polymer matrix, the SVE electrodes exerted an embedding effect to reduce polysulfides migration. The thiosulfate/polythionate protective layer derived from the terminal hydroxyl group of SVE also ensured the cycle stability of SVE electrodes during cycling. As a result, optimized SVE electrodes deliver a high reversible specific capacity of 1248 mA h g(-1) at rates of 0.1 C, together with a stable cycling performance of no capacity decay per cycle over more than 400 cycles. This work provides an effective strategy for the practical application of organosulfur polymers Li-S batteries and inspires the exploration of the reaction mechanism of epoxy/allyl compound/sulfur system.

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