4.6 Article

Redox Reactions of Ag(I)/Ag and Ferrocenium/Ferrocene in 1-Butyl-1-methylpyrrolidinium Bis(fluorosulfonyl)amide Ionic Liquid

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 170, Issue 4, Pages -

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/acc9e2

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The electrode reactions of Ag(I)/Ag and ferrocenium/ferrocene were investigated in an ionic liquid, with the potential of Ag(I)/Ag acting as a reference electrode reaction. The reversible electrode reaction of ferrocenium/ferrocene was observed, and the coordination ability of the ionic liquid was found to be slightly stronger than a different ionic liquid. The diffusion coefficients and standard rate constant for the electrode reactions were determined, providing insights into the properties of the ionic liquid system.
The electrode reactions of Ag(I)/Ag and ferrocenium/ferrocene (Fc(+)/Fc) were investigated in an ionic liquid, 1-butyl-1-methylpyrrolidinium bis(fluorosulfonyl)amide (BMPFSA). The potential of Ag(I)/Ag depended on the logarithm of the concentration of Ag(I), as predicted by the Nernst equation, indicating the Ag(I)/Ag can be used as a reference electrode reaction in BMPFSA. The reversible electrode reaction of Fc(+)/Fc was observed in BMPFSA by cyclic voltammetry. The donor number of BMPFSA was estimated to be 13 from the difference in the formal potentials of Ag(I)/Ag and Fc(+)/Fc, indicating the coordination ability of FSA(-) was slightly stronger than that of bis(trifluoromethylsulfonyl)amide (TFSA(-)). The diffusion coefficients (D) of Fc and Fc(+) were (5.7 +/- 0.7) and (3.3 +/- 0.2) x 10(-7) cm(2) s(-1), respectively. The ratio of D of Fc(+) against that of Fc was smaller than those in TFSA(-)-type ionic liquids, reflecting the higher charge density of FSA(-). The standard rate constant (k(0)) of Fc(+)/Fc was estimated to be (5.4 +/- 1.1) x 10(-3) cm s(-1). The apparent activation energy for k(0) was close to the activation energy for D, suggesting the electrode reaction of Fc(+)/Fc can be regarded as the outer sphere electron transfer reaction with a very small reorganization energy. (c) 2023 The Author(s). Published on behalf of The Electrochemical Society by IOP Publishing Limited.

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