Publication:
Guidelines for the voltammetric study of electrode reactions with coupled chemical kinetics at an arbitrary electrode geometry

dc.contributor.authorLópez Tenés, Manuela
dc.contributor.authorLaborda Ochando, Eduardo
dc.contributor.authorMolina Gómez, Ángela
dc.contributor.authorCompton, Richard G.
dc.contributor.departmentQuímica Física
dc.date.accessioned2021-03-23T17:36:56Z
dc.date.available2021-03-23T17:36:56Z
dc.date.copyright© 2019, American Chemical Society,
dc.date.issued2019-04-02
dc.description.abstractA powerful, unified, and simplifying mathematical approach for the theoretical treatment of first-order chemical kinetics coupled to interfacial charge transfers at electrodes of arbitrary geometry and size, both uniformly accessible and nonuniformly accessible to the electroactive species, is presented. The general CEC mechanism at spherical and disc electrodes is considered to test the validity and benefits of such an approach, based on the application of the so-called kinetic steady state, that enables the reduction of the multivariable problem of kinetic-diffusive differential equations to a single variable problem of a diffusion-only differential equation. This is solved both analytically and numerically, showing how this approach leads to general, simple, and efficient solutions for the study of the influence of coupled chemical kinetics on the voltammetric response. The voltammetry of the CEC mechanism is analyzed as a function of the kinetics and thermodynamics of the preceding and subsequent chemical reactions and of the electrode size (from macroelectrodes to ultramicroelectrodes) and shape (spherical and disc). Comparison with the responses of the CE, EC, and E mechanisms is included, proposing diagnosis criteria and procedures for quantitative analysis of experimental data.
dc.formatapplication/pdfes
dc.format.extent24es
dc.identifier.citationAnalytical Chemistry 2019, 91 (9), 6072–6079
dc.identifier.doihttps://doi.org/10.1021/acs.analchem.9b00616
dc.identifier.eissn1520-6882
dc.identifier.issn0003-2700
dc.identifier.urihttp://hdl.handle.net/10201/105542
dc.languageenges
dc.publisherACS Publicationses
dc.relationÁmbito del proyecto: regional. Agencia/entidad financiadora: Fundación Séneca de la Región de Murcia. Convocatoria: Convocatoria de ayudas a las unidades y grupos de excelencia científica de la Región de Murcia (Programa Séneca 2014). Nombre del proyecto: Advances in the study of charge transfer processes at static and dynamic micro-and nano-interfaces Código: 19887/GERM/15 es
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/acs.analchem.9b00616es
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAnalytical theoryes
dc.subjectNumerical simulationes
dc.subjectVoltammetryes
dc.subjectElectron transfer mechanismes
dc.subjectMicroelectrodees
dc.subject.otherCDU::5 - Ciencias puras y naturales::54 - Química::544 - Química físicaes
dc.titleGuidelines for the voltammetric study of electrode reactions with coupled chemical kinetics at an arbitrary electrode geometryes
dc.typeinfo:eu-repo/semantics/articlees
dc.type.versioninfo:eu-repo/semantics/acceptedVersión
dspace.entity.typePublicationes
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relation.isAuthorOfPublicationaa4883f0-68e2-47a9-a892-bdc401a759b9
relation.isAuthorOfPublication76c9e61c-d6ed-4278-a76d-d16f3d651298
relation.isAuthorOfPublication.latestForDiscoveryc21fa975-63b4-4c4e-998b-ef102a5540b8
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