Marcus-Hush-Chidsey theory of electron transfer applied to voltammetry: A review

被引:149
作者
Henstridge, Martin C. [1 ]
Laborda, Eduardo [1 ]
Rees, Neil V. [1 ]
Compton, Richard G. [1 ]
机构
[1] Univ Oxford, Dept Chem, Phys & Theoret Chem Lab, Oxford OX1 3QZ, England
基金
英国工程与自然科学研究理事会;
关键词
Electrode kinetics; Marcus-Hush-Chidsey model; Butler-Volmer model; Solution-phase redox couple; Voltammetry; DIFFERENTIAL-PULSE VOLTAMMETRY; ELECTROCHEMICAL RATE-CONSTANT; CLASSICAL SOLVENT DYNAMICS; CHARGE-TRANSFER PROCESSES; SQUARE-WAVE VOLTAMMETRY; OSMIUM AQUO COMPLEX; TRANSFER KINETICS; REDOX CENTERS; ACTIVATION PARAMETERS; SPHERICAL ELECTRODES;
D O I
10.1016/j.electacta.2011.10.026
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The application of the Marcus-Hush-Chidsey (MHC) formalism to heterogeneous electron transfer processes is reviewed and compared with the commonly employed Butler-Volmer (BV) approach. The MHC model is potentially more powerful than BV since it enables us to analyze the electrode kinetics in terms of the microscopic nature of the electroactive species, electrode and solvent. Despite having been studied fairly extensively in the case of surface-bound redox couples, its application to heterogeneous electron transfer reactions has been limited. Here, we review the use of the MHC approach for the analysis of both surface-bound and solution phase redox systems and its suitability as a model for the parameterisation of electrode kinetics. Results obtained for several slow electrode reactions using cyclic voltammetry and reverse scan square wave voltammetry are reviewed which reveal that the simple MHC model does not always give a satisfactory fit to experimental data in contrast to BV parameterisation. Possible physical reasons for the experimental deviations from simple MHC theory are examined. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:12 / 20
页数:9
相关论文
共 75 条
[1]   PHYSICAL ASPECTS OF CHARGE-TRANSFER THEORY [J].
ALEXANDROV, IV .
CHEMICAL PHYSICS, 1980, 51 (03) :449-457
[2]   Ultrafast voltammetry for probing interfacial electron transfer in molecular wires [J].
Amatore, Christian ;
Maisonhaute, Emmanuel ;
Schollhorn, Bernd ;
Wadhawan, Jay .
CHEMPHYSCHEM, 2007, 8 (09) :1321-1329
[3]   Studies of charge transfer at liquid | liquid interfaces and bilayer lipid membranes by scanning electrochemical microscopy [J].
Amemiya, S ;
Ding, ZF ;
Zhou, JF ;
Bard, AJ .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2000, 483 (1-2) :7-17
[4]  
[Anonymous], 2001, ELECTROCHEMICAL METH
[5]   NEW EXPERIMENTAL-EVIDENCE CONCERNING THE MAGNITUDE OF THE ACTIVATION PARAMETERS FOR FAST HETEROGENEOUS ELECTRON-TRANSFER REACTIONS [J].
BARANSKI, AS ;
WINKLER, K ;
FAWCETT, WR .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1991, 313 (1-2) :367-375
[6]   ELECTROCHEMISTRY AT OMEGA-HYDROXY THIOL COATED ELECTRODES .3. VOLTAGE INDEPENDENCE OF THE ELECTRON-TUNNELING BARRIER AND MEASUREMENTS OF REDOX KINETICS AT LARGE OVERPOTENTIALS [J].
BECKA, AM ;
MILLER, CJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (06) :2657-2668
[7]   SYMMETRY FACTOR AND TRANSFER COEFFICIENT - SOURCE OF CONFUSION IN ELECTRODE KINETICS [J].
BOCKRIS, JO ;
NAGY, Z .
JOURNAL OF CHEMICAL EDUCATION, 1973, 50 (12) :839-843
[8]   Studies in heterogeneous equilibria. Part II - The kinetic interpretation of the nernst theory of electromotive force. [J].
Butler, JAV .
TRANSACTIONS OF THE FARADAY SOCIETY, 1924, 19 (03) :0729-0733
[9]   CLASSICAL SOLVENT DYNAMICS AND ELECTRON-TRANSFER .2. MOLECULAR ASPECTS [J].
CALEF, DF ;
WOLYNES, PG .
JOURNAL OF CHEMICAL PHYSICS, 1983, 78 (01) :470-482
[10]   CLASSICAL SOLVENT DYNAMICS AND ELECTRON-TRANSFER .1. CONTINUUM THEORY [J].
CALEF, DF ;
WOLYNES, PG .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (18) :3387-3400