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Electrochemistry of tris(2,2′-bipyridyl) cobalt(II) in ionic liquids and aprotic molecular solvents on glassy carbon and platinum electrodes

journal contribution
posted on 2015-10-20, 00:00 authored by D Cabral, Patrick HowlettPatrick Howlett, Jenny PringleJenny Pringle, X Zhang, D MacFarlane
The tris(2,2′-bipyridyl) complexes of cobalt(II) and (III) ([Co(bpy)3]2+/3+) produce a redox couple of great interest in thermoelectrochemical cells and dye sensitized solar cells including both types of devices based on ionic liquid electrolytes. We present a systematic study of the electrochemistry of [Co(bpy)3]2+ [NTf2]-2 in two ionic liquids (ILs) based on the 1-ethyl-3-methylimidazolium (C2mim) cation and two ILs based on the 1-butyl-1-methylpyrrolidinium cation (C4mpyr), as well as three aprotic molecular solvents. Platinum (Pt) and glassy carbon (GC) working electrodes were compared. In all solvents better electrochemical responses were observed on GC, which yielded higher currents in the cyclic voltammograms and lower rate constants for the redox reaction. The [Co(bpy)3]1+/2+ couple is also readily observed, but this redox reaction is chemically irreversible, possibly because the [Co(bpy)3]1+ complex dissociates. However, the [Co(bpy)3]1+/2+ reaction is chemically reversible in all of the solvents studied, except 3-methoxypropionitrile, if excess of 2,2′-bipyridyl is added to the solution.

History

Journal

Electrochimica acta

Volume

180

Pagination

419 - 426

Publisher

Elsevier

Location

Amsterdam, The Netherlands

ISSN

0013-4686

Language

eng

Publication classification

C Journal article; C1 Refereed article in a scholarly journal

Copyright notice

2015, Elsevier