Elsevier

Computers & Chemistry

Volume 20, Issue 2, June 1996, Pages 209-218
Computers & Chemistry

Versatile computer-based instrumentation for the application of three-dimensional voltammetry

https://doi.org/10.1016/0097-8485(95)00053-4Get rights and content

Abstract

A versatile and inexpensive computer-based instrument for the application of 3-D voltammetry has been developed. The computerized system is easily interfaced to most potentiostats and allows for automated control, multi-function data acquisition, digital transformation of data and complex analysis. An evaluation of system performance as well as a few selected examples illustrating the general advantages of 3-D voltammetry are presented.

References (29)

  • J.E. Anderson et al.

    J. Electroanal. Chem. Interfacial Electrochem.

    (1983)
  • J.E. Anderson et al.

    J. Electroanal. Chem. Interfacial Electrochem.

    (1989)
  • A.M. Bond et al.

    Anal. Chim. Acta.

    (1984)
  • F. David et al.

    Anal. Chim. Acta.

    (1994)
  • D.R. Ferrier et al.

    J. Electroanal. Chem. Interfacial Electrochem.

    (1973)
  • D.R. Ferrier et al.

    J. Electroanal. Chem. Interfacial Electrochem.

    (1973)
  • W. Huang et al.

    Anal. Chim. Acta

    (1995)
  • J.J. Scanlon et al.

    Anal. Chim. Acta

    (1984)
  • K. Seto et al.

    J. Electroanal. Chem. Interfacial Electrochem.

    (1987)
  • D.E. Tallman et al.

    J. Electroanal. Chem. Interfacial Electrochem.

    (1990)
  • W. Thormann et al.

    J. Electroanal. Chem. Interfacial Electrochem.

    (1988)
  • J.E. Anderson et al.

    Anal. Chem.

    (1981)
  • J.E. Anderson et al.

    Am. Lab.

    (1981)
  • J.E. Anderson et al.

    Anal. Chem.

    (1982)
  • Cited by (5)

    • Three-dimensional voltammetry: Use of chronoamperometric E-t-i data to achieve second-order advantage

      2020, Analytica Chimica Acta
      Citation Excerpt :

      It is well known that the resolution between two overlapping voltammetric processes depends largely upon the half-wave potential (E1/2) values, the concentration ratios and the kinetics of the electron transfer [21]. Thus, for example, if two overlapping processes are kinetically different in the context of the electron transfer being the rate determining step, then the multi-time-domain electrochemical measurements could provide a useful way of discriminating against one of the processes, as long as measurements were made at longer time domains [22]. The work presented here aimed at the evaluation of E-t-i data in association with second-order calibration techniques in the development of electroanalytical methods.

    • Three-dimensional voltammetry assisted by parametric signal fitting: A new perspective for the electrochemical evaluation of metal binding in the presence of electrodic adsorption

      2013, Analytica Chimica Acta
      Citation Excerpt :

      Although many efforts have been devoted to minimise or modelize this phenomenon [14–21], it still constitutes a serious drawback in the study of metal complexation. In the present work we revisit the methodology of three-dimensional voltammetry, consisting on the measurement of currents vs. potential vs. time by means of consecutive chronoamperograms at increasing potential steps [22–26]. In previous studies such methodology had been mostly applied for qualitative purposes.

    Present address: CSIRO Division of Minerals, P.O. Box 124, Port Melbourne, Victoria 3207, Australia.

    View full text