Cargando…

Nanosponge-Based Composite Gel Polymer Electrolyte for Safer Li-O(2) Batteries

Li-O(2) batteries represent a promising rechargeable battery candidate to answer the energy challenges our world is facing, thanks to their ultrahigh theoretical energy density. However, the poor cycling stability of the Li-O(2) system and, overall, important safety issues due to the formation of Li...

Descripción completa

Detalles Bibliográficos
Autores principales: Amici, Julia, Torchio, Claudia, Versaci, Daniele, Dessantis, Davide, Marchisio, Andrea, Caldera, Fabrizio, Bella, Federico, Francia, Carlotta, Bodoardo, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8156716/
https://www.ncbi.nlm.nih.gov/pubmed/34067902
http://dx.doi.org/10.3390/polym13101625
Descripción
Sumario:Li-O(2) batteries represent a promising rechargeable battery candidate to answer the energy challenges our world is facing, thanks to their ultrahigh theoretical energy density. However, the poor cycling stability of the Li-O(2) system and, overall, important safety issues due to the formation of Li dendrites, combined with the use of organic liquid electrolytes and O(2) cross-over, inhibit their practical applications. As a solution to these various issues, we propose a composite gel polymer electrolyte consisting of a highly cross-linked polymer matrix, containing a dextrin-based nanosponge and activated with a liquid electrolyte. The polymer matrix, easily obtained by thermally activated one pot free radical polymerization in bulk, allows to limit dendrite nucleation and growth thanks to its cross-linked structure. At the same time, the nanosponge limits the O(2) cross-over and avoids the formation of crystalline domains in the polymer matrix, which, combined with the liquid electrolyte, allows a good ionic conductivity at room temperature. Such a composite gel polymer electrolyte, tested in a cell containing Li metal as anode and a simple commercial gas diffusion layer, without any catalyst, as cathode demonstrates a full capacity of 5.05 mAh cm(−2) as well as improved reversibility upon cycling, compared to a cell containing liquid electrolyte.