Issue 20, 2022

Halogenation of Li7La3Zr2O12 solid electrolytes: a combined solid-state NMR, computational and electrochemical study

Abstract

Garnet-based solid electrolytes have been proposed as promising candidates for next generation all-solid-state batteries. Whilst multiple cation substitution studies of these garnets have been undertaken to try and improve their overall performance, anion doping of garnets has rarely been attempted, owing to the synthetic challenges associated with this particular doping strategy. In this work, we present the halogenation (F, Cl) of the solid state electrolyte Li7La3Zr2O12 (LLZO) via a low temperature solid state synthetic route using PTFE and PVC polymers. A reduction in tetragonal distortion (F incorporation) and a tetragonal to cubic phase transition (Cl incorporation) is observed in halogenated LLZO, suggesting the replacement of O2− with F or Cl is associated with the creation of lithium vacancies. Combined solid-state NMR and computational studies support the presence of F or Cl in halogenated LLZO. The effects of surface fluorination were also investigated for Al-doped LLZO (Li6.4Al0.2La3Zr2O12, LLAZO) with the results suggesting that this strategy has the ability to prevent full dendrite penetration at high current densities (up to 10 mA cm−2).

Graphical abstract: Halogenation of Li7La3Zr2O12 solid electrolytes: a combined solid-state NMR, computational and electrochemical study

Supplementary files

Article information

Article type
Paper
Submitted
25 Aug 2021
Accepted
21 Feb 2022
First published
04 Mai 2022
This article is Open Access
Creative Commons BY license

J. Mater. Chem. A, 2022,10, 11172-11185

Halogenation of Li7La3Zr2O12 solid electrolytes: a combined solid-state NMR, computational and electrochemical study

B. Dong, A. R. Haworth, S. R. Yeandel, M. P. Stockham, M. S. James, J. Xiu, D. Wang, P. Goddard, K. E. Johnston and P. R. Slater, J. Mater. Chem. A, 2022, 10, 11172 DOI: 10.1039/D1TA07309E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements