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Dual Cation Exchanged Poly(ionic liquid)s as Magnesium Conducting Electrolytes AITranslate

University of Notre Dame; University of Notre Dame; University of Notre Dame; University of Notre Dame; University of Notre Dame; University of Notre Dame
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Publisher: ACS
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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.

KeyWords AITranslate

polymer electrolytes magnesium battery polymerized ionic liquids poly(ionic liquid)s ionic conductivity
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.9b00614

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Citation Information:

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.

quote

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}