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A single-ion conducting covalent organic framework for aqueous rechargeable Zn-ion batteries

Despite their potential as promising alternatives to current state-of-the-art lithium-ion batteries, aqueous rechargeable Zn-ion batteries are still far away from practical applications. Here, we present a new class of single-ion conducting electrolytes based on a zinc sulfonated covalent organic fr...

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Detalles Bibliográficos
Autores principales: Park, Sodam, Kristanto, Imanuel, Jung, Gwan Yeong, Ahn, David B., Jeong, Kihun, Kwak, Sang Kyu, Lee, Sang-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8162792/
https://www.ncbi.nlm.nih.gov/pubmed/34123199
http://dx.doi.org/10.1039/d0sc02785e
Descripción
Sumario:Despite their potential as promising alternatives to current state-of-the-art lithium-ion batteries, aqueous rechargeable Zn-ion batteries are still far away from practical applications. Here, we present a new class of single-ion conducting electrolytes based on a zinc sulfonated covalent organic framework (TpPa-SO(3)Zn(0.5)) to address this challenging issue. TpPa-SO(3)Zn(0.5) is synthesised to exhibit single Zn(2+) conduction behaviour via its delocalised sulfonates that are covalently tethered to directional pores and achieve structural robustness by its β-ketoenamine linkages. Driven by these structural and physicochemical features, TpPa-SO(3)Zn(0.5) improves the redox reliability of the Zn metal anode and acts as an ionomeric buffer layer for stabilising the MnO(2) cathode. Such improvements in the TpPa-SO(3)Zn(0.5)–electrode interfaces, along with the ion transport phenomena, enable aqueous Zn–MnO(2) batteries to exhibit long-term cyclability, demonstrating the viability of COF-mediated electrolytes for Zn-ion batteries.