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Tailoring the Periphery Aliphatic Group of Cathode Organosulfde for Rechargeable High-Performance All-Solid-State Lithium Battery
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作者 Yan Chen Mingcong Yang +5 位作者 Wei Hu Tao Chen Jun Li Shun Wang Huile Jin Jichang Wang 《Energy & Environmental Materials》 2025年第2期44-52,共9页
Organic cathode materials exhibit higher energy storage capacity,their poor cyclability due to dissolution in liquid organic electrolytes remains a challenge.However,recently,the electrochemical behavior of organopoly... Organic cathode materials exhibit higher energy storage capacity,their poor cyclability due to dissolution in liquid organic electrolytes remains a challenge.However,recently,the electrochemical behavior of organopolysulfides incorporating N-heterocycles unveils promising cathode materials with stable cycling performance.Herein,the integration of organosulfides salt as cathodes with solid electrolytes,exemplified by sodium allyl(methyl)carbamodithioate and sodium diethylcarbamodithioate with a polymer solid electrolyte of polyethylene oxide and LiTFSI,addresses the poor electrochemical stability of organic electrodes.Comparative analysis highlights sodium allyl(methyl)carbamodithioate's superior electrochemical performance and stability compared with sodium diethylcarbamodithioate,emphasizing the efficacy of periphery aliphatic modification in enhancing electrode capacity,rate performance,and electrochemical stability for organosulfide materials within all-solid-state lithium organic batteries.We also explore the origin of periphery aliphatic modification in these enhancing electrochemical performances by kinetic analysis and thermodynamic analysis.Furthermore,employing density functional theory calculations and ex situ FTIR experiments elucidates the critical role of the N-C=S structure in the energy storage mechanism.This research advances organic cathode design within organosulfide materials,unlocking the potential of allsolid-state lithium organic batteries with enhanced cyclability,propelling the development of next-generation energy storage systems. 展开更多
关键词 all-solid-state lithiumorganicbatteries organiccathodematerials organosulfide materials peripheryaliphaticdesign polyethyleneoxide
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Synthesis of poly[methyl(3,3,3-trifluoropropyl)siloxane]-b-poly(ethylene oxide) block copolymers 被引量:3
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作者 Xiao-li ZHAN Bi CHEN +3 位作者 Qing-hua ZHANG Ling-min YI Bo JIANG Feng-qiu CHEN 《Journal of Zhejiang University-Science A(Applied Physics & Engineering)》 SCIE EI CAS CSCD 2008年第9期1304-1308,共5页
A series of new amphiphilic poly[methyl(3,3,3-trifluoropropyl)siloxane]-b-poly(ethylene oxide) (PMTFPS-b-PEO) diblock copolymers with different ratios of hydrophobic segment to hydrophilic segment were prepared ... A series of new amphiphilic poly[methyl(3,3,3-trifluoropropyl)siloxane]-b-poly(ethylene oxide) (PMTFPS-b-PEO) diblock copolymers with different ratios of hydrophobic segment to hydrophilic segment were prepared by coupling reactions of end-functlonal PMTFPS and PEO homopolymers. Copolymers were shown to be well defined and narrow molecular weight distribution (MWD) (1.07-1.3) by characterizations such as gel permeation chromatography (GPC) and ^1H-nudear magnetic resonance (^1H-NMR). 展开更多
关键词 Block copolymers POLYSILOXANES FLUOROPOLYMERS Synthesis polyethyleneoxide
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