Interfacial Interaction of Multifunctional GQDs Reinforcing Polymer Electrolytes For All‐Solid‐State Li Battery
Solid‐state polymer electrolytes are highly anticipated for next generation lithium ion batteries with enhanced safety and energy density. However, a major disadvantage of polymer electrolytes is their low ionic conductivity at room temperature. In order to enhance the ionic conductivity, here, grap...
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Veröffentlicht in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2023-08, Vol.19 (33), p.e2301275-n/a |
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Sprache: | eng |
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Zusammenfassung: | Solid‐state polymer electrolytes are highly anticipated for next generation lithium ion batteries with enhanced safety and energy density. However, a major disadvantage of polymer electrolytes is their low ionic conductivity at room temperature. In order to enhance the ionic conductivity, here, graphene quantum dots (GQDs) are employed to improve the poly (ethylene oxide) (PEO) based electrolyte. Owing to the increased amorphous areas of PEO and mobility of Li+, GQDs modified composite polymer electrolytes achieved high ionic conductivity and favorable lithium ion transference numbers. Significantly, the abundant hydroxyl groups and amino groups originated from GQDs can serve as Lewis base sites and interact with lithium ions, thus promoting the dissociation of lithium salts and providing more ion pathways. Moreover, lithium dendrite is suppressed, associated with high transference number, enhanced mechanical properties and steady interface stability. It is further observed that all solid‐state lithium batteries assembled with GQDs modified composite polymer electrolytes display excellent rate performance and cycling stability.
Graphene quantum dots have many excellent properties. Here, graphene quantum dots are employed as additives to PEO‐based polymer solid electrolytes, which improve the performance of composite electrolytes in multiaspect. The assembled solid‐state battery has enhanced cycle stability and improved rate performance. |
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ISSN: | 1613-6810 1613-6829 |
DOI: | 10.1002/smll.202301275 |