A Nernstian electron source model for the ac voltammetric response of a reversible surface redox reaction using large-amplitude ac voltages

A new model that predicts the reversible ac voltammetric peak profile of a surface redox reaction for an arbitrary choice of the ac voltage amplitude is described. The model is termed the Nernstian Electron Source (NES) model since it is based on a superposition of the fluctuating ac voltage onto a Nernstian distribution of states. The model extends previous theoretical treatments of ac voltammetry which were based on equivalent circuit models that are strictly valid only for small voltage perturbations. Two ferrocene-based monolayer systems were studied to test the predictions of the new model. The dependence of peak height on voltage amplitude for one such monolayer system deviated from the predictions of the older equivalent circuit model at modest amplitudes (Eac<25 mV) but was in excellent agreement with the predictions from the NES model at all measured amplitudes. The use of large-amplitude ac voltammetry for increasing signal amplitude and for driving otherwise slow surface redox reactions at appreciable rates is also demonstrated.

[1]  Š. Komorsky-Lovrič,et al.  Square-wave voltammetry of quasi-reversible surface redox reactions , 1995 .

[2]  W. Kuhr,et al.  Cyclic voltammetry with harmonic lock-in detection: Applications to flow streams , 1996 .

[3]  H. Finklea,et al.  Electrolyte and temperature effects on long range electron transfer across self-assembled monolayers , 1993 .

[4]  D. Mandler,et al.  Applications of self-assembled monolayers in electroanalytical chemistry , 1996 .

[5]  C. Yu,et al.  Soluble Ferrocene Conjugates for Incorporation into Self-Assembled Monolayers. , 1999, The Journal of organic chemistry.

[6]  K. G. Olsen,et al.  Self-assembled monolayers and enzyme electrodes: Progress, problems and prospects , 1995 .

[7]  T. T. Wooster,et al.  A New Way of Using ac Voltammetry To Study Redox Kinetics in Electroactive Monolayers , 1998 .

[8]  E. Lam,et al.  Electron Transfer at Electrodes through Conjugated “Molecular Wire” Bridges , 1999 .

[9]  M. Senda,et al.  Theory of A.c. Polarization and A.c. Polarography and Voltammetry of Surface Redox Reaction , 1979 .

[10]  J. Reeves,et al.  Application of square wave voltammetry to strongly adsorbed quasireversible redox molecules , 1993 .

[11]  Edmond F. Bowden,et al.  The distribution of standard rate constants for electron transfer between thiol-modified gold electrodes and adsorbed cytochrome c , 1996 .

[12]  E. Laviron A.C. Polarography and faradaic impedance of strongly adsorbed electroactive species: Part III. Theoretical complex plane analysis for a surface redox reaction , 1979 .

[13]  S. Creager,et al.  Voltammetry of Redox-Active Groups Irreversibly Adsorbed onto Electrodes. Treatment Using the Marcus Relation between Rate and Overpotential , 1994 .

[14]  J. J. O'Dea,et al.  Characterization of quasi-reversible surface processes by square-wave voltammetry , 1993 .

[15]  T. Wink,et al.  Self-assembled monolayers for biosensors. , 1997, The Analyst.

[16]  K. T. Kawagoe,et al.  Sinusoidal Voltammetry for the Analysis of Carbohydrates at Copper Electrodes , 1997 .