The in situ solid electrolyte interphase formed using solid electrolyte additives for highly reversible zinc metal anodes

Zhao, J; Zhao, YH; Xu, D; Li, MX; Dai, ZQ; Wang, ML; Rajendran, S; Zhang, XY; Qin, JQ

Abstract

Coating artificial solid electrolyte interphases (ASEIs) on zinc anodes is regarded as a direct and effective approach to stabilize them; however, conventional coating methods result in poor conductivity and susceptibility to delamination. Herein, we successfully synthesized GOZIF8 powder using graphene oxide and zeolitic imidazolate framework-8, followed by its incorporation into 2 M zinc sulfate (ZSO) electrolyte to facilitate the formation of in situ SEIs (ISEIs) on zinc sheets. The ISEI changed the solvation process during Zn2+ ion deposition and induced the epitaxial deposition of Zn2+ along the (110) and (101) crystal planes. Consequently, Zn//Zn symmetrical cells incorporating GOZIF8 electrolyte additives exhibited a stable cycling performance exceeding 4500 hours at a polarization potential of 20 mV under 1 mA cm?2 and 1 mA h cm?2. Additionally, the GOZIF8 electrolyte in the Zn//NH4V4O10 full cells demonstrated superior coulombic efficiency and enhanced capacity, with a self-discharge capacity retention rate of up to 93.5% following a 24-hours relaxation interval. Overall, the approach of engineering the electrolyte to construct ISEI presents a novel strategy to stabilize zinc anode reversibility, providing a promising avenue for the commercial utilization of zinc-ion batteries. © 2025 The Royal Society of Chemistry.

Más información

Título según WOS: The in situ solid electrolyte interphase formed using solid electrolyte additives for highly reversible zinc metal anodes
Título según SCOPUS: The in situ solid electrolyte interphase formed using solid electrolyte additives for highly reversible zinc metal anodes
Título de la Revista: Journal of Materials Chemistry A
Volumen: 13
Número: 33
Editorial: Royal Society of Chemistry
Fecha de publicación: 2025
Página de inicio: 27607
Página final: 27617
Idioma: English
DOI:

10.1039/d5ta03562g

Notas: ISI, SCOPUS