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Ultra-High-Capacity Lithium Metal Batteries Based on Multi-Electron Redox Reaction of Organopolysulfides including Conductive Organic Moieties.


ABSTRACT: Recently, organic polysulfides have been synthesized as cathode active materials exceeding the battery performance of sulfur. However, the conventional organic polysulfides have exhibited capacities lower than the theoretical capacity of sulfur because the π-organic moieties do not conjugate with the sulfur chains. In this work, the organopolysulfides, synthesized via inverse vulcanization using disulfide compounds, exhibited higher capacities equal to the theoretical capacity of sulfur because of enhanced electronic conductivity based on the conjugation between organic moieties and sulfur chains. Furthermore, the organopolysulfide including 1,3-dhitiol-2-thione moiety exhibited the highest capacity because of the enhanced electronic conductivity. This finding will pave the way to develop next-generation rechargeable batteries.

SUBMITTER: Shimizu T 

PROVIDER: S-EPMC9866748 | biostudies-literature | 2023 Jan

REPOSITORIES: biostudies-literature

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Ultra-High-Capacity Lithium Metal Batteries Based on Multi-Electron Redox Reaction of Organopolysulfides including Conductive Organic Moieties.

Shimizu Takeshi T   Tanifuji Naoki N   Nishio Kosuke K   Tanaka Yuma Y   Tsukaguchi Yuta Y   Tsubouchi Kentaro K   Nakamura Fumiya F   Shokura Naoko N   Noguchi Mariko M   Fujimori Hiroki H   Kimura-Suda Hiromi H   Date Yusuke Y   Aoki Kaoru K   Yoshikawa Hirofumi H  

Polymers 20230109 2


Recently, organic polysulfides have been synthesized as cathode active materials exceeding the battery performance of sulfur. However, the conventional organic polysulfides have exhibited capacities lower than the theoretical capacity of sulfur because the π-organic moieties do not conjugate with the sulfur chains. In this work, the organopolysulfides, synthesized via inverse vulcanization using disulfide compounds, exhibited higher capacities equal to the theoretical capacity of sulfur because  ...[more]

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