Published July 1, 2013 | Version v1
Journal article

Generator–collector electroanalysis at tin-doped indium oxide–epoxy–tin-doped indium oxide junction electrodes

  • 1. Department of Chemistry, University of Bath, Bath BA2 7AY (United Kingdom)

Description

Generator–collector electroanalysis approaching the nanomolar level is demonstrated for the reduction of Ru(NH3)63+ in aqueous (NH4)2SO4 (saturated, as a naturally low-oxygen electrolyte medium) and at tin-doped indium oxide (ITO) electrodes. ITO–ITO double band and double plate geometries are compared. Cyclic voltammetric detection down into the sub-micromolar concentration level is readily achieved at co-planar ITO–ITO double plate junction electrodes with typically 4 μm inter-electrode gap, 5 mm length, and ca. 62 μm average inter-electrode trench depth. Trace oxygen (ca. 60 μM) is shown to enhance both generator and collector currents and the cathodic excess current |Igenerator| − |Icollector| is employed to estimate the bimolecular rate constant for Ru(NH3)62+ reacting with O2, k2 = 104 mol−1 dm3 s−1

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2012.08.121

Additional details

Identifiers

DOI
10.1016/j.electacta.2012.08.121;
PII
S0013-4686(12)01426-0;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
101
Journal Page Range
p. 196-200
ISSN
0013-4686
CODEN
ELCAAV

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45052848
Subject category
S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
Descriptors DEI
AMMONIA; DOPED MATERIALS; ELECTRODES; ELECTROLYTES; INDIUM OXIDES; OXYGEN; POLAROGRAPHY; REACTION KINETICS; SENSORS; TIN
Descriptors DEC
CHALCOGENIDES; ELEMENTS; HYDRIDES; HYDROGEN COMPOUNDS; INDIUM COMPOUNDS; KINETICS; MATERIALS; METALS; NITROGEN COMPOUNDS; NITROGEN HYDRIDES; NONMETALS; OXIDES; OXYGEN COMPOUNDS

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.