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![The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F54498.jpg&w=3840&q=50)
The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique
Published on: November 28, 2016
Stannaborates: tuning the ion conductivity of dodecaborate salts with tin substitution
Thomas A Hales1, Kasper T Møller1,2, Terry D Humphries1
1Physics and Astronomy, Institute for Energy Transition, Curtin University, GPO Box U1987, Perth, WA 6845, Australia. mark.paskevicius@gmail.com.
Abstract:
Metal substituted dodecaborate anions can be coupled with alkali metal cations to have great potential as solid-state ion conductors for battery applications. A tin atom can replace a B-H unit within an unsubstituted dodecaborate cage to produce a stable, polar divalent anion. The chemical and structural change in forming a stannaborate results in a modified crystal structure of respective group 1 metal salts, and as a result, improves the material's ion conductivity. Li2B11H11Sn shows high ion conductivity of ∼8 mS cm-1 at 130 °C, similar to the state-of-the-art LiCB11H12 at these temperatures, however, obtaining high ion conductivity at room temperature is not possible with pristine alkali metal stannaborates.
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