lCyclic voltammetry of a solid polymer solution of a tetrathiafulvalene (TT
F) derivative showed different behaviours depending on the nature of the el
ectrolyte anion. A lower potential and current peak for the second redox re
action in the presence of perchlorate revealed a specific interaction betwe
en this anion and the TTF dication. This effect also indicates a coupling b
etween the physical diffusion and electron self-exchange during the voltamm
etric scan. No interaction between the TTF dication and triflimide or TFSI-
bis (trifluoromethanesulfonyl) imide-anion was observed. This confirms the
exceptional softness of this anion and underlines the role that the nature
of the electrolyte anion could play on both the ionic and the electronic co
nductivities of the electrode polymer materials. (C) 2001 Elsevier Science
B.V. All rights reserved.