Cargando…

Interface Engineering via Ti(3)C(2)T(x) MXene Electrolyte Additive toward Dendrite-Free Zinc Deposition

Zinc metal batteries have been considered as a promising candidate for next-generation batteries due to their high safety and low cost. However, their practical applications are severely hampered by the poor cyclability that caused by the undesired dendrite growth of metallic Zn. Herein, Ti(3)C(2)T(...

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Chuang, Wu, Cuiping, Gu, Xingxing, Wang, Chao, Wang, Qinghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8006525/
https://www.ncbi.nlm.nih.gov/pubmed/34138322
http://dx.doi.org/10.1007/s40820-021-00612-8
Descripción
Sumario:Zinc metal batteries have been considered as a promising candidate for next-generation batteries due to their high safety and low cost. However, their practical applications are severely hampered by the poor cyclability that caused by the undesired dendrite growth of metallic Zn. Herein, Ti(3)C(2)T(x) MXene was first used as electrolyte additive to facilitate the uniform Zn deposition by controlling the nucleation and growth process of Zn. Such MXene additives can not only be absorbed on Zn foil to induce uniform initial Zn deposition via providing abundant zincophilic-O groups and subsequently participate in the formation of robust solid-electrolyte interface film, but also accelerate ion transportation by reducing the Zn(2+) concentration gradient at the electrode/electrolyte interface. Consequently, MXene-containing electrolyte realizes dendrite-free Zn plating/striping with high Coulombic efficiency (99.7%) and superior reversibility (stably up to 1180 cycles). When applied in full cell, the Zn-V(2)O(5) cell also delivers significantly improved cycling performances. This work provides a facile yet effective method for developing reversible zinc metal batteries. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40820-021-00612-8.