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Journal ArticleDOI

Formic acid oxidation at platinized platinum electrodes: Part V. A further study of catalytic effect of preadsorbed sulfur

TLDR
In this article, the authors investigated the effect of preadsorbed sulfur on the growth and stripping of the sulfur layer in the presence of adsorbed formic acid in the form of a sulfur layer from SO2 solutions.
About
This article is published in Journal of Electroanalytical Chemistry.The article was published on 1979-10-25. It has received 12 citations till now. The article focuses on the topics: Sulfur.

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Citations
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Journal ArticleDOI

Deactivation of Pt/VC proton exchange membrane fuel cell cathodes by SO2, H2S and COS

TL;DR: In this article, the deactivation behavior of commercial Pt on Vulcan carbon (Pt/VC) membrane electrode assemblies (MEAs) is determined when exposed to 1.5ppm (dry) of SO 2, H 2 S, or COS in air for 3, 12, and 24h while held at a constant potential of 0.6
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Oxidation of formic acid at platinum microparticles dispersed in a polyaniline matrix: Influence of long-range order and metal-polymer interaction

TL;DR: In this paper, the effects of long-range order and deposition of platinum microparticles on the activity of polyaniline films synthesized at various temperatures have been investigated.
Journal ArticleDOI

Potential dependence of sulfur dioxide poisoning and oxidation at the cathode of proton exchange membrane fuel cells

TL;DR: In this article, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were employed to investigate changes in the cathode after the introduction of SO2, and the decay in performance of the proton exchange membrane fuel cell was ascribed to the increasing of the charge transfer resistance (Rct) caused by the loss of the electrochemical surface area (ECA).
Journal ArticleDOI

Operational Performance Recovery of SO2-Contaminated Proton Exchange Membrane Fuel Cells

TL;DR: In this paper, the performance of proton exchange membrane fuel cells (PEMFCs) was examined after 3 h of exposure to 1 ppm SO 2 in air at 60°C and 48.3 kPa g (7 psi) and relative humidity of 100 | 50% (anode | cathode).
Journal ArticleDOI

The study of electrode processes of sulphur dioxide on platinized electrode by the radiochemical method

TL;DR: In this paper, the adsorption of sulphur dioxide and the electrode reactions of adsorbed molecules at a platinized platinum electrode were studied by potentiodynamic and radiometric techniques.
References
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Journal ArticleDOI

Origin of Activation Effects of Acetonitrile and Mercury in Electrocatalytic Oxidation of Formic Acid

TL;DR: In this article, it was shown that in the presence of catalyst poisons such as acetonitrile or mercury, the currents for formic acid oxidation, measured in the potential range +0.4 to + 0.8V E(H) at Pt can be substantially increased.
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Electrochemical oxidation of formic acid at noble metals: Catalytic effects of foreign metal monolayers

TL;DR: In this article, the catalytic effects of a submonolayer of lead on noble metals have been discussed and discussed in terms of a previously published model, and theoretical analysis of these effects is presented.
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Two forms of chemisorbed sulfur on platinum and related studies

TL;DR: The effect of temperature on the potentiodynamic oxidation of adsorbed sulfur layers on platinum, obtained from H 2 S or SO 2 was studied in this paper, where two distinct peaks were observed at 80°C, oxidation peak I (at 0.97 V) corresponding to the weakly bound sulfur and oxidation peak II (at 1.10 V) representing the strongly bound sulfur.
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Adsorption and oxidation of organic compounds on a platinum electrode partly covered by adsorbed sulphur

TL;DR: In this paper, the dependence of the non-stationary currents of formic acid, formaldehyde and methanol on the degree of coverage of the platinum electrode by adsorbed sulphur and the effect of adaption of sulphur on the electrooxidation of methenol and formaldehyde have been studied.
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The nature of species adsorbed on platinum from SO2 solutions

TL;DR: In this paper, it was shown that at θS 0.9, the formation of a partial bilayer on top of the first layer can be explained by the presence of two forms of "difficultly reducible" oxygen.
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