Potential step cyclic voltammetry for the study of electrode reaction mechanisms

1970 ◽  
Vol 24 (1) ◽  
pp. A1-A5 ◽  
Author(s):  
L. Papouchado ◽  
J. Bacon ◽  
R.N. Adams

A general computational strategy is presented for the calculation of the chronoamperometric responses arising from potential-step experiments at rotating disc electrodes. The method is applicable to a wide range of electrode reaction mechanisms and theoretical results are given for single- and double-potential-step experiments for ECE, DISP1, DISP2, EC' and CE reactions. For the last, the treatment is extended to cover the case where reactants have grossly unequal diffusion coefficients. Steadystate behaviour is also deduced. The extent to which the various mechanistic pathways can be distinguished is identified and the necessary experiments defined.


2019 ◽  
Vol 91 (19) ◽  
pp. 12220-12227 ◽  
Author(s):  
Gareth F. Kennedy ◽  
Jie Zhang ◽  
Alan M. Bond

1996 ◽  
Vol 49 (8) ◽  
pp. 901 ◽  
Author(s):  
E Wagnerczauderna ◽  
MK Kalinowski

Cyclic voltammetry has been used to measure formal potentials of seven aromatic ketone/ketyl radical anion systems in benzonitrile, acetonitrile , propylene carbonate, acetone, N,N- dimethylformamide, N-methylpyrrolidin-2-one, dimethyl sulfoxide and hexamethylphosphoric triamide. The values measured in each solvent obey the Hammett- Streitwieser equation; the reaction constants were found to depend on the solvent acidity and basicity expressed by acceptor and donor numbers, respectively. The results are discussed in terms of the solvation of the products and reactants of the electrode reaction.


CORROSION ◽  
1987 ◽  
Vol 43 (2) ◽  
pp. 118-126 ◽  
Author(s):  
B. D. Yan ◽  
G. W. Warren ◽  
P. Wynblatt

1988 ◽  
Vol 33 (11) ◽  
pp. 1489-1492 ◽  
Author(s):  
Katsuo Takahashi ◽  
Yasuhiro Yamamoto ◽  
Kiyoshi Matsuda ◽  
Hiroshi Yamazaki

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