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Elucidating the pressure-induced enhancement of ionic conductivity in sodium closo-hydroborate electrolytes for all-solid-state batteries
Hydroborates are an emerging class of solid electrolytes for all-solid-state batteries. Here, we investigate the impact of pressure on the crystal structure and ionic conductivity of a close-hydroborate salt consisting of Na(2)B(10)H(10) and Na(2)B(12)H(12). Two Na(2)B(10)H(10):Na(2)B(12)H(12) ratio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160155/ https://www.ncbi.nlm.nih.gov/pubmed/37159820 http://dx.doi.org/10.1007/s10853-022-08121-8 |
Sumario: | Hydroborates are an emerging class of solid electrolytes for all-solid-state batteries. Here, we investigate the impact of pressure on the crystal structure and ionic conductivity of a close-hydroborate salt consisting of Na(2)B(10)H(10) and Na(2)B(12)H(12). Two Na(2)B(10)H(10):Na(2)B(12)H(12) ratios were studied, 1:1 and 1:3. The anions of the as-synthesized powder with 1:1 ratio crystallize in a single face-centered cubic phase, while the anions of the powder with 1:3 ratio crystallize in a single monoclinic phase. After applying pressure to densify the powder into a pellet, a partial phase transformation into a body-centered cubic (BCC) phase is observed for both ratios. The BCC content saturates at 50 weight percent (wt%) at 500 MPa for the 1:1 ratio and at 77 wt% at 1000 MPa for the 1:3 sample. The room temperature sodium-ion conductivity follows an analogous trend. For the 1:1 ratio, it increases from 2 × 10(–4) Scm(−1) at 10 wt% BCC content to about 1.0 × 10(–3) Scm(−1) at 50 wt% BCC content. For the 1:3 ratio, it increases from 1.3 × 10(–5) Scm(−1) at 11.9 wt% BCC to 8.1 × 10(–4) Scm(−1) at 71 wt% BCC content. Our results show that pressure is a prerequisite to achieve high sodium-ion conductivity by formation of the highly conductive BCC phase. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10853-022-08121-8. |
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