Study of redox active C-60/Pd films by simultaneous cyclic voltammetry andpiezoelectric microgravimetry at an electrochemical quartz crystal microbalance
K. Winkler et al., Study of redox active C-60/Pd films by simultaneous cyclic voltammetry andpiezoelectric microgravimetry at an electrochemical quartz crystal microbalance, J ELCHEM SO, 147(7), 2000, pp. 2597-2603
The formation and properties of redox active C-60/Pd films on gold electrod
es of quartz oscillators were investigated by simultaneous cyclic voltammet
ry and piezoelectric microgravimetry at a quartz crystal microbalance. The
films were prepared by electroreduction of solutions of C-60 and [Pd-II(CH3
COO)(2)](3) in 0.1 mol dm(-3) tetra(n-butyl)ammonium perchlorate in acetoni
trile-toluene (1:4, v:v). The composition of the solution from which the fi
lms were prepared significantly influenced the pattern of the film growth.
The present results confirm that palladium clusters are codeposited with th
e C-60/Pd film ii the palladium complex to C-60 ratio was high. The reduced
polymer film becomes partially electrochemically inactive at a sufficientl
y negative potential range. However, this electrically inactive film can be
oxidized at very positive potentials. For charge compensation, the tetra(n
-butyl)ammonium countereations enter the film during its electroreduction a
nd are expelled from the film during electro-oxidation. At relatively high
potential scan rates, only the outermost layers of the film that are in dir
ect contact with the bathing solution are electrochemically active. At low
scan rates, however, the bulk film material is also active. At very negativ
e potentials, the film is removed from the electrode. The size of the tetra
(n-alkyl)ammonium countereation is a major factor that determines both the
electrochemical properties of the C-60/Pd films and their stability with re
spect to dissolution. (C) 2000 The Electrochemical Society.