Electropolymerized organic N/P bipolar cathode toward high energy and high power density sodium dual-ion batteries
Sodium dual ion batteries (SDIBs) have received considerable attention recently for large-scale energy storage systems due to their low cost and inherent safety. Nevertheless, SDIBs remain a subject of investigation as efficient cathode materials for high energy densities and are still under develop...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 12; no. 48; pp. 33624 - 33631 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
10.12.2024
|
Subjects | |
Online Access | Get full text |
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Summary: | Sodium dual ion batteries (SDIBs) have received considerable attention recently for large-scale energy storage systems due to their low cost and inherent safety. Nevertheless, SDIBs remain a subject of investigation as efficient cathode materials for high energy densities and are still under development. Bipolar organic compounds stand out for their ability to combine both the merits of high voltage of p-type and high capacity of n-type electrode materials. Herein, we developed a bipolar organic cathode bearing n-type anthraquinone (AQ) and p-type triphenylamine (TPA) through
in situ
electropolymerization for efficient sodium dual-ion storage. The combined high capacity of n-type and high voltage of p-type materials serve to achieve exceptional electrochemical performances of SDIBs in terms of high energy density and high power density. Experimental and theoretical calculations validate the bipolar energy storage mechanism. This work broadens the chemical scope of bipolar organic cathode materials for state-of-the-art SDIBs.
PTPA-AQ, an
in situ
electropolymerized bipolar organic cathode for sodium dual-ion batteries, achieving 426 Wh kg
−1
energy density after 300 cycles at 0.2 A g
−
¹, with 3000 cycle stability at 5 A g
−
¹ and 14.9 kW kg
−
¹ power density. |
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Bibliography: | https://doi.org/10.1039/d4ta07077a Electronic supplementary information (ESI) available. See DOI ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d4ta07077a |