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Locked Coplanar Conformation Boosts Rapid Electron/Ion Transport in Linear Polyimide Cathodes for Sodium-Ion Storage
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作者 Jingjing Chen Yongcong Huang +10 位作者 Huimin Yuan Mingyang Yang Jing Hu Hongzhi Wang Yulin Cao Fangchang Zhang Guiyu Liu Lei Wang Shuai Gu Chen Liu Zhouguang Lu 《Chinese Journal of Chemistry》 2026年第4期437-444,共8页
Organic materials have obtained unprecedented attention as emerging electrodes for sodium-ion batteries(SIBs),but they suffer from poor cycling stability and rate performance.Herein,we develop a simple strategy via lo... Organic materials have obtained unprecedented attention as emerging electrodes for sodium-ion batteries(SIBs),but they suffer from poor cycling stability and rate performance.Herein,we develop a simple strategy via locking the coplanarity to tune the electron and ion transport in linear polyimide for sodium-ion batteries.From unlocked and flexible molecular chain to spatially locked molecular chain,the polyimide cathodes possess better structural stability and higher electronic conductivity,exhibiting better cycling stability and higher reversible capacity.Moreover,the locked-in coplanar conformation endows the polyimide cathode with large surface area and rich porosity,leading to a rapid ion transport,which synergizes with the good electronic conductivity to improve the rate performance of the SIBs.As a result,the optimized polyimide electrode displays high capacity retentions of 99%after 100 cycles at 50 mA·g^(-1)and 100%after 3000 cycles at 1000 mA·g^(-1).This work expands the palette to design organic electrodes for high-performance SIBs. 展开更多
关键词 Organic electrode Locked structure Electron and ion transport Radical intermediates Sodium-ion batteries Organic cathode material Electrochemistry Reaction mechanisms
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