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High-rate, high-capacity electrochemical energy storage in hydrogen-bonded fused aromatics
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK). KTH Royal Institute of Technology, Sweden.ORCID iD: 0000-0003-2221-2285
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Number of Authors: 72023 (English)In: Joule, E-ISSN 2542-4351, Vol. 7, no 5, p. 986-1002Article in journal (Refereed) Published
Abstract [en]

Designing materials for electrochemical energy storage with short charging times and high charge capacities is a longstanding challenge. The fundamental difficulty lies in incorporating a high density of redox couples into a stable material that can efficiently conduct both ions and electrons. We report all-organic, fused aromatic materials that store up to 310 mAh g−1 and charge in as little as 33 s. This performance stems from abundant quinone/imine functionalities that decorate an extended aromatic backbone, act as redox-active sites, engage in hydrogen bonding, and enable a delocalized high-rate energy storage with stability upon cycling. The extended conjugation and hydrogen-bonding-assisted bulk charge storage contrast with the surface-confined or hydration-dependent behavior of traditional inorganic electrodes.

Place, publisher, year, edition, pages
2023. Vol. 7, no 5, p. 986-1002
National Category
Materials Chemistry
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URN: urn:nbn:se:su:diva-226142DOI: 10.1016/j.joule.2023.03.011ISI: 001137001100001Scopus ID: 2-s2.0-85153908738OAI: oai:DiVA.org:su-226142DiVA, id: diva2:1833518
Available from: 2024-02-01 Created: 2024-02-01 Last updated: 2024-02-01Bibliographically approved

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Li, Jian

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