Towards understanding silver-carbon composite interlayers in anode-free solid-state batteries
Dominic Spencer-Jolly a, Varnika Agarwal b, Peter Bruce b
a School of Metallurgy and Materials, University of Birmingham, Elms Road, Birmingham, B15 2SE, UK
b Department of Materials, University of Oxford, Parks Road, Oxford, OX1 3PH, UK
Proceedings of 24th International Conference on Solid State Ionics (SSI24)
Devices for a Net Zero World
London, United Kingdom, 2024 July 14th - 19th
Organizers: John Kilner and Stephen Skinner
Oral, Dominic Spencer-Jolly, presentation 272
Publication date: 10th April 2024

Anode-free solid-state batteries, in which the lithium anode is formed in situ during the first charge, could deliver a step-change in cell energy densities. However, at charge rates on the order of 1 mA cm2, plating of Li at the current collector/solid electrolyte interface is highly inhomogeneous, and dendrites (filaments of Li metal) are observed to penetrate through the solid electrolyte resulting in cell failure. Recent work has suggested that introduction of a silver-carbon composite interlayer between the solid electrolyte and current collector can prevent dendrite ingress into the solid electrolyte whilst promoting more homogeneous deposition of Li metal.[1] 

In this work, we investigate silver-carbon composite interlayers, revealing the structural changes within the interlayer during charge and discharge, and the rate dependence of these changes. We go on to investigate the homogeneity of Li-Ag alloy and Li metal formation at the current collector with and without silver nanoparticles present in the interlayer, and how this affects the processes of charge and discharge. We demonstrate dendrite-free charge at 2 mA cm2 and reveal the origin of the failure of the interlayer at higher rates.[2]

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