A new way of using ac voltammetry to study redox kinetics in electroactive monolayers

被引:226
作者
Creager, SE [1 ]
Wooster, TT
机构
[1] Clemson Univ, Dept Chem, Clemson, SC 29634 USA
[2] Westminster Coll, Dept Chem, New Wilmington, PA 16172 USA
[3] Clin Micro Sensors Inc, Pasadena, CA 91105 USA
关键词
D O I
10.1021/ac980482l
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new protocol for analyzing variable-frequency ac voltammetry (acv) data to obtain electron-transfer rate constants for redox-active groups immobilized in monolayer films on electrodes is described. The protocol involves plotting the ratio of the peak current to the background current as a function of the log of frequency and then fitting the plot to a calculated curve obtained using the Randles equivalent circuit model. The fitting procedure is particularly straightforward since it involves just two adjustable fitting parameters and can usually be performed manually in a spreadsheet. Advantages of the new method include the following: (1) it requires fewer adjustable fitting parameters than the conventional impedance analysis performed in the complex-plane format; (2) because there are fewer fitting parameters, there is less chance of the fit yielding a false convergence; (3) nonideal effects associated with a distribution of rate constants are apparently revealed in a particularly intuitive and easily interpreted manner; (4) data analysis can be accomplished without the need for information on the phase of the ac current signal; and (5) analysis can be performed on extremely small voltammetric peaks that would be difficult if not impossible to analyze in the complex-plane format due to the overwhelming effects of background currents. Electron-transfer rate constants obtained by this method for ferrocene oxidation/reduction in mixed monolayers of N-(mercaptopentadecyl)ferrocenecarboxamide (FcCONH-C-15-SH) and 16-mercaptohexadecanol (HO-Cls-SH) on gold were in the range of 9-13 s(-1), in good agreement with values obtained using a complex nonlinear least-squares method to fit data in the conventional complex-plane format and also with previously reported values for this system obtained by analysis of fast-scan de cyclic voltammetry data. Analysis of the redox kinetics for an ensemble of just 1.8 fmol or 1 x 10(9) molecules of ferrocene is also demonstrated.
引用
收藏
页码:4257 / 4263
页数:7
相关论文
共 38 条
[1]   Contemporary issues in electron transfer research [J].
Barbara, PF ;
Meyer, TJ ;
Ratner, MA .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (31) :13148-13168
[2]  
Bard A., 1994, INTEGRATED CHEM SYST
[3]   ELECTRON-TRANSFER KINETICS OF REDOX CENTERS ANCHORED TO METAL-SURFACES - WEAK VS STRONG OVERLAP REACTION PATHWAYS [J].
BARR, SW ;
GUYER, KL ;
LI, TTT ;
LIU, HY ;
WEAVER, MJ .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1984, 131 (07) :1626-1631
[4]   THE ANALYSIS OF ELECTRODE IMPEDANCES COMPLICATED BY THE PRESENCE OF A CONSTANT PHASE ELEMENT [J].
BRUG, GJ ;
VANDENEEDEN, ALG ;
SLUYTERSREHBACH, M ;
SLUYTERS, JH .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1984, 176 (1-2) :275-295
[5]   DISTANCE DEPENDENCE OF THE LOW-TEMPERATURE ELECTRON-TRANSFER KINETICS OF (FERROCENYLCARBOXY)-TERMINATED ALKANETHIOL MONOLAYERS [J].
CARTER, MT ;
ROWE, GK ;
RICHARDSON, JN ;
TENDER, LM ;
TERRILL, RH ;
MURRAY, RW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (10) :2896-2899
[6]   FREE-ENERGY AND TEMPERATURE-DEPENDENCE OF ELECTRON-TRANSFER AT THE METAL-ELECTROLYTE INTERFACE [J].
CHIDSEY, CED .
SCIENCE, 1991, 251 (4996) :919-922
[7]   Voltammetric peak broadening for cytochrome c/alkanethiolate monolayer structures: Dispersion of formal potentials [J].
Clark, RA ;
Bowden, EF .
LANGMUIR, 1997, 13 (03) :559-565
[8]   CONSEQUENCES OF MICROSCOPIC SURFACE-ROUGHNESS FOR MOLECULAR SELF-ASSEMBLY [J].
CREAGER, SE ;
HOCKETT, LA ;
ROWE, GK .
LANGMUIR, 1992, 8 (03) :854-861
[9]   ON THE INTERPLAY BETWEEN INTERFACIAL POTENTIAL DISTRIBUTION AND ELECTRON-TRANSFER KINETICS IN ORGANIZED MONOLAYERS ON ELECTRODES [J].
CREAGER, SE ;
WEBER, K .
LANGMUIR, 1993, 9 (03) :844-850
[10]   UNUSUAL QUASI-REVERSIBILITY (UQR) OR APPARENT NON-KINETIC HYSTERESIS IN CYCLIC VOLTAMMETRY - AN ELABORATION UPON THE IMPLICATIONS OF N-SHAPED FREE-ENERGY RELATIONSHIPS AS EXPLANATION [J].
FELDBERG, SW ;
RUBINSTEIN, I .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1988, 240 (1-2) :1-15