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 in | RSC advances Vol. 5; no. 22; pp. 1796 - 1713 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Royal Society of Chemistry
01.01.2015
|
Subjects | |
Online Access | Get full text |
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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. |
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Bibliography: | 10.1039/c4ra15976d Electronic supplementary information (ESI) available: Further electrochemical characterization. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c4ra15976d |