Dicationic organic salts are an interesting class of solid-state electrolyte materials due to their unique structure. Here we present, for the first time, the synthesis and characterization of three dicationic-FSI salts, 1,2-bis(N-methylpyrrolidinium)ethane bi(bis(fluorosulfonyl)imide) ([C -Pyrr1][FSI] ), 1,2-bis(N-ethylpyrrolidinium)ethane bi(bis(fluorosulfonyl)imide) ([C -Pyrr2][FSI] ) and 1,2-bis(N-n-propylpyrrolidinium)ethane bi(bis(fluorosulfonyl)imide) ([C -Pyrr3][FSI] ). The structure and dynamics of the organic salts were probed using variable temperature solid-state NMR and were compared with the thermal and transport properties. The investigation revealed that [C -Pyrr1][FSI] , with shorter alkyl-side chains on the dication, displayed increased transport properties compared to [C -Pyrr2][FSI] and [C -Pyrr3][FSI] . To determine the proficiency of these dicationic-FSI salts as electrolyte materials for battery applications, 10 mol% and 50 mol% lithium bis(fluorosulfonyl)imide (LiFSI) was mixed with [C -Pyrr1][FSI] and [C -Pyrr2][FSI] . Increased transport properties were observed for [C -Pyrr1][FSI] /10 mol % LiFSI in comparison to [C -Pyrr2][FSI] /10 % LiFSI, while pulse field gradient NMR analysis revealed the highest Li self-diffusion ratio for [C -Pyrr1][FSI] /50 % LiFSI out of the four Li-salt-containing mixtures.
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http://dx.doi.org/10.1002/cssc.202202249 | DOI Listing |
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