Redox-active polyimide-polyether block copolymers as electrode materials for lithium batteries

Redox-active polyimide-polyether multi-block copolymers were synthesized by polycondensation reaction of aromatic dianhydrides with α-ω-diamino poly(ethylene oxide). Polyimide- b -polyether block copolymers showed microphase separation between a hard-polyimide domain and a soft-polyether domain as o...

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Published inRSC advances Vol. 5; no. 22; pp. 1796 - 1713
Main Authors Hernández, Guiomar, Casado, Nerea, Coste, Raphaël, Shanmukaraj, Devaraj, Rubatat, Laurent, Armand, Michel, Mecerreyes, David
Format Journal Article
LanguageEnglish
Published Royal Society of Chemistry 01.01.2015
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Summary:Redox-active polyimide-polyether multi-block copolymers were synthesized by polycondensation reaction of aromatic dianhydrides with α-ω-diamino poly(ethylene oxide). Polyimide- b -polyether block copolymers showed microphase separation between a hard-polyimide domain and a soft-polyether domain as observed by Atomic Force Microscopy. The block copolymers were investigated as cathodes for polymer/lithium metal batteries. Polymer cathodes were formulated where the block copolymer had a dual role as active material and binder, with a small amount of carbon black (15 wt%). Naphthalene polyimides showed higher discharge voltages, higher specific capacities as well as better cycling performance, compared to pyromellitic polyimides. The longest PEO blocks resulted in a better performance as electrodes. The best performing naphthalene polyimide- b -PEO2000 presented an excellent value of discharge capacity of 170 mA h g −1 , stable after 100 cycles at a current density of 1Li + /5 h and considering the polyimide as the active material. The average discharge plateaus were 2.51 V and 2.37 V vs. Li + /Li. Excellent cyclability of polyimide-polyether block copolymers used as cathode materials in lithium batteries was demonstrated.
Bibliography:10.1039/c4ra15976d
Electronic supplementary information (ESI) available: Further electrochemical characterization. See DOI
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ISSN:2046-2069
2046-2069
DOI:10.1039/c4ra15976d