Comparison of voltammetric responses of toluene and xylenes at iron(III)-doped, bismuth(V)-doped, and undoped beta-lead dioxide film electrodes in 0.50 M H2SO4

Citation
Se. Treimer et al., Comparison of voltammetric responses of toluene and xylenes at iron(III)-doped, bismuth(V)-doped, and undoped beta-lead dioxide film electrodes in 0.50 M H2SO4, J ELCHEM SO, 148(12), 2001, pp. E459-E463
Citations number
24
Categorie Soggetti
Physical Chemistry/Chemical Physics","Material Science & Engineering
Journal title
JOURNAL OF THE ELECTROCHEMICAL SOCIETY
ISSN journal
00134651 → ACNP
Volume
148
Issue
12
Year of publication
2001
Pages
E459 - E463
Database
ISI
SICI code
0013-4651(200112)148:12<E459:COVROT>2.0.ZU;2-J
Abstract
Voltammetric activities are compared for the designated compounds in 0.50 M H2SO4 at the specified film electrodes configured as rotated disks. The ef fective number of electrons (n(eff), equiv mol(-1)) calculated from the Kou tecky-Levich plot is 3.1 +/- 0.2 for toluene oxidation at the Fe-PbO2 elect rode, compared to 2.0 +/- 0.05 and 4.1 +/- 0.3 at the Bi-PbO2 and PbO2 elec trodes, respectively. Gas chromatography-mass spectrometry data confirm tha t the primary product of toluene oxidation is benzyl alcohol (2 equiv mol(- 1)) at the Fe-PbO2 electrode with production of small amounts of benzaldehy de (4 equiv mol(-1))and benzoic acid ( equiv mol(-1)) X-ray photoelectron s pectroscopy data indicate the ratio of Fe: Pb is ca. 1:100 (atom: atom) in the Fe-PbO2 films. By comparison, a Bi: Pb ratio of 33:100 (atom: atom) is easily attained in Bi-PbO2 films. Nevertheless, the apparent heterogeneous rate constant (k(app), cm s(-1)) for toluene oxidation is larger at the Fe- PbO2 electrode (6.5 +/- 0.06 x 10(-3)) compared to the Bi-PbO2 electrode (2 .0 +/- 0.05 x 10(-3)). X-ray absorption near-edge structure data confirm sp eculation that iron exists in the 3+ oxidation state with octahedral coordi nation by O atoms in Fe-PbO2 films. The large activity of the Fe-PbO2 elect rode is attributed to the benefit of adsorption of aromatic molecules at Fe (III) sites. (C) 2001 The Electrochemical Society.