Dual Cation Exchanged Poly(ionic liquid)s as Magnesium Conducting Electrolytes AITranslate
Abstract AITranslate
Solid-state magnesium-ion conductors are desired for next-generation battery applications. Here we investigate magnesium conducting polymer electrolytes produced through dual cation exchange of a poly(ionic liquid) by mixing 1-butyl-3-methylimidazolium poly[4-styrenesulfonyl(trifluoromethanesulfonyl)imide] (BMIPSTFSI) with the magnesiated analogue Mg(PSTFSI)2. An ionic conductivity of 8.6 × 10–5 S cm–1 at 80 °C was achieved for the poly(ionic liquid), and conductivity did not significantly decrease with magnesium content up to 5 mol % Mg(PSTFSI)2 (3.8 × 10–5 S cm–1). The characteristic poly(ionic liquid) ion-to-ion correlation peak was observable via X-ray scattering at these low magnesium contents but disappeared at higher magnesium loadings. Polarization experiments were performed in Cu/Mg cells, resulting in sparse magnesium-rich particle-like deposits on the Cu electrode. With a lack of widespread deposition, however, either the magnesium electrodeposition or the magnesium stripping from the magnesium metal is unfavorable for this electrolyte.
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DOI:https://doi.org/10.1021/acsapm.9b00614
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Solid-state magnesium-ion conductors are desired for next-generation battery applications. Here we investigate magnesium conducting polymer electrolytes produced through dual cation exchange of a poly(ionic liquid) by mixing 1-butyl-3-methylimidazolium poly[4-styrenesulfonyl(trifluoromethanesulfonyl)imide] (BMIPSTFSI) with the magnesiated analogue Mg(PSTFSI)2. An ionic conductivity of 8.6 × 10–5 S cm–1 at 80 °C was achieved for the poly(ionic liquid), and conductivity did not significantly decrease with magnesium content up to 5 mol % Mg(PSTFSI)2 (3.8 × 10–5 S cm–1). The characteristic poly(ionic liquid) ion-to-ion correlation peak was observable via X-ray scattering at these low magnesium contents but disappeared at higher magnesium loadings. Polarization experiments were performed in Cu/Mg cells, resulting in sparse magnesium-rich particle-like deposits on the Cu electrode. With a lack of widespread deposition, however, either the magnesium electrodeposition or the magnesium stripping from the magnesium metal is unfavorable for this electrolyte.
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| GB/T 7714-2015 | [1] Bumjun Park, Hunter O. Ford, Laura C. Merrill, et al. ACS Applied Polymer Materials, 2019(1). DOI:10.1021/acsapm.9b00614. |
| MLA | [1] Bumjun Park, et al., ACS Applied Polymer Materials, no. 1, 2019, https://doi.org/10.1021/acsapm.9b00614. |
| APA | [1] Bumjun Park, Hunter O. Ford, Laura C. Merrill, Jiacheng Liu, Loyal P. Murphy, & Jennifer L. Schaefer. (2019). ACS Applied Polymer Materials(1). https://doi.org/10.1021/acsapm.9b00614 |
| IEEE | [1] Bumjun Park, Hunter O. Ford, Laura C. Merrill, Jiacheng Liu, Loyal P. Murphy, and Jennifer L. Schaefer, ACS Applied Polymer Materials, no. 1, 2019, doi: 10.1021/acsapm.9b00614. keywords: {polymer electrolytes;magnesium battery;polymerized ionic liquids;poly(ionic liquid)s;ionic conductivity} |
