Issue 40, 2019

The influence of silica surface groups on the Li-ion conductivity of LiBH4/SiO2 nanocomposites

Abstract

Lithium borohydride is a promising lithium ion conductor for all-solid-state batteries. However, the compound only exhibits high ionic conductivity at elevated temperatures, typically above 110 °C. It was shown that the addition of oxides such as silica or alumina increases the room temperature ionic conductivity by 3 orders of magnitude. The origin of this remarkable effect is not yet well understood. Here, we investigate the influence of oxide surface groups on the ionic conductivity of LiBH4/SiO2 nanocomposites. We systematically varied the density and nature of the surface groups of mesoporous silica by heat treatment at different temperatures, or surface functionalization, and subsequently prepared LiBH4/SiO2 nanocomposites by melt infiltration. The ionic conductivity is strongly influenced by the heat treatment temperature, hence the density of the free surface silanol groups. Replacing some of the silanol groups with hydrophobic surface groups resulted in an order of magnitude reduction of the room temperature ionic conductivity, suggesting that their presence is crucial to obtain high ionic conductivity in the nanocomposites. This systematic study and insight provide a basis for further exploration of the impact of surface groups, and for the rational design of novel solid-state nanocomposite electrolytes via interface engineering.

Graphical abstract: The influence of silica surface groups on the Li-ion conductivity of LiBH4/SiO2 nanocomposites

Supplementary files

Article information

Article type
Paper
Submitted
30 Jul 2019
Accepted
16 Sep 2019
First published
28 Sep 2019
This article is Open Access
Creative Commons BY-NC license

Phys. Chem. Chem. Phys., 2019,21, 22456-22466

The influence of silica surface groups on the Li-ion conductivity of LiBH4/SiO2 nanocomposites

P. Ngene, S. F. H. Lambregts, D. Blanchard, T. Vegge, M. Sharma, H. Hagemann and P. E. de Jongh, Phys. Chem. Chem. Phys., 2019, 21, 22456 DOI: 10.1039/C9CP04235K

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