TY - JOUR
T1 - Giving physical insight into the Butler-Volmer model of electrode kinetics
T2 - Application of asymmetric Marcus-Hush theory to the study of the electroreductions of 2-methyl-2-nitropropane, cyclooctatetraene and europium(III) on mercury microelectrodes
AU - Henstridge, M.C.
AU - Laborda, E.
AU - Wang, Y.
AU - Suwatchara, D.
AU - Rees, N.
AU - Compton, R.G.
AU - Molina, A.
AU - Martínez-Ortiz, F.
N1 - Copyright 2012 Elsevier B.V., All rights reserved.
PY - 2012/5/1
Y1 - 2012/5/1
N2 - The asymmetric Marcus-Hush (MH) model for electrode kinetics is applied to the kinetic study of the electroreduction of 2-methyl-2-nitropropane in acetonitrile, cyclooctatetraene in dimethylsulfoxide and europium(III) in aqueous solution, using mercury microhemispheres as working electrodes. This kinetic model includes the possibility of the oxidative and reductive processes having different reorganization energies due to differences between the force constants of the electroactive species. For each redox couple, the response obtained in cyclic and square wave voltammetries can be fitted satisfactorily with the four-parameter asymmetric MH model. From the fitting of the voltammograms the values of the kinetic parameters are extracted and analyzed in terms of physical properties of the electroactive species. A comparison of the asymmetric model against the simpler, phenomenological Butler-Volmer (BV) approach is discussed, as well as a possible physical interpretation for the BV transfer coefficient.
AB - The asymmetric Marcus-Hush (MH) model for electrode kinetics is applied to the kinetic study of the electroreduction of 2-methyl-2-nitropropane in acetonitrile, cyclooctatetraene in dimethylsulfoxide and europium(III) in aqueous solution, using mercury microhemispheres as working electrodes. This kinetic model includes the possibility of the oxidative and reductive processes having different reorganization energies due to differences between the force constants of the electroactive species. For each redox couple, the response obtained in cyclic and square wave voltammetries can be fitted satisfactorily with the four-parameter asymmetric MH model. From the fitting of the voltammograms the values of the kinetic parameters are extracted and analyzed in terms of physical properties of the electroactive species. A comparison of the asymmetric model against the simpler, phenomenological Butler-Volmer (BV) approach is discussed, as well as a possible physical interpretation for the BV transfer coefficient.
UR - http://www.scopus.com/inward/record.url?partnerID=yv4JPVwI&eid=2-s2.0-84859642041&md5=c5d86cc876d0cf43be51ebb87cd6b887
U2 - 10.1016/j.jelechem.2012.02.028
DO - 10.1016/j.jelechem.2012.02.028
M3 - Article
AN - SCOPUS:84859642041
SN - 1572-6657
VL - 672
SP - 45
EP - 52
JO - Journal of Electroanalytical Chemistry
JF - Journal of Electroanalytical Chemistry
ER -