Abstract
The redox couples M/M+ of the Group I alkali metals Lithium, Sodium, Potassium, Rubidium and Caesium have been extensively investigated in a room temperature ionic liquid (IL) and compared for the first time. Cyclic voltammetric experiments in the IL N-butyl-N-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([C4mpyrr][NTf2]) and subsequent simulation of the data has allowed the determination of the formal potential (Ef0 vs. ferrocene/ferrocenium), standard electrochemical rate constant (k) and transfer coefficient (α) for each couple in the group. The trend in Ef0 in [C4mpyrr][NTf2] is remarkably similar to the established trend in the common battery electrolyte, propylene carbonate.
Original language | English |
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Pages (from-to) | 276-280 |
Number of pages | 5 |
Journal | Chemical Physics Letters |
Volume | 492 |
Issue number | 4-6 |
DOIs | |
Publication status | Published - 7 Jun 2010 |