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Journal ArticleDOI

Cyclic voltammetric studies on iridium electrodes in sulphuric acid solutions

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TLDR
In this paper, it was shown that iridium phase oxides can be formed in 1 or 0.1 M H2SO4 with a coverage of one oxygen atom per iridium surface site at 1.5 V on a triangular potential sweep.
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This article is published in Journal of Electroanalytical Chemistry.The article was published on 1974-09-25. It has received 161 citations till now. The article focuses on the topics: Iridium & Oxide.

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Citations
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Synthesis and Activities of Rutile IrO2 and RuO2 Nanoparticles for Oxygen Evolution in Acid and Alkaline Solutions

TL;DR: This study shows that these r-RuO2 and r-IrO2 NPs can serve as a benchmark in the development of active OER catalysts for electrolyzers, metal-air batteries, and photoelectrochemical water splitting applications.
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Electrical stimulation of excitable tissue: design of efficacious and safe protocols.

TL;DR: The physical basis for electrical stimulation of excitable tissue, as used by electrophysiological researchers and clinicians in functional electrical stimulation, is presented with emphasis on the fundamental mechanisms of charge injection at the electrode/tissue interface.
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Developments and perspectives of oxide-based catalysts for the oxygen evolution reaction

TL;DR: In this article, the authors summarized previous and most recent theoretical predictions and experimental outcomes in the field of oxide-based catalysts for the oxygen evolution reaction (OER), both operating in acidic and alkaline environments.
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Hydrogen Oxidation and Evolution Reaction Kinetics on Carbon Supported Pt, Ir, Rh, and Pd Electrocatalysts in Acidic Media

TL;DR: In this article, the hydrogen oxidation and evolution reaction (HOR/HER) behavior of carbon supported metal (Pt, Ir, Rh, Pd) nanoparticle electrocatalysts is studied using the H2 pump approach, in a proton exchange membrane fuel cell (PEMFC) setup.
References
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Journal ArticleDOI

Limiting oxygen coverage on platinized platinum; Relevance to determination of real platinum area by hydrogen adsorption

TL;DR: In this paper, a limiting oxygen coverage is found on platinized platinum electrodes and identified as a monolayer of chemisorbed oxygen atoms, and the problems involved in interpreting hydrogen adsorption measurements in terms of real electrode areas are discussed.
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A study of the dissolution of platinum, palladium, rhodium and gold electrodes in 1 m sulphuric acid by cyclic voltammetry

TL;DR: In this paper, it is emphasized that metal dissolution currents should not be ignored when examining electrochemical processes on noble metals at anodic potentials, and evidence in support of an anodic mechanism for noble metal corrosion has been obtained from studies of the variation of dissolution rate with both potential and temperature.
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The nature of adsorbed oxygen on rhodium, palladium and gold electrodes

TL;DR: In this paper, a basis for distinguishing between chemisorption and phase formation is presented, which can be used for accurate measurement of real surface area of rhodium and palladium electrodes.
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Hydrogen adsorption on platinum, iridium and rhodium electrodes at reduced temperatures and the determination of real surface area

TL;DR: In this article, the saturation hydrogen coverage and the real surface area of an electrode were determined directly from the voltammogram of platinum and iridium electrodes in 5 M sulphuric acid at −72°C.
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A ring-disk electrode study of the current/potential behaviour of platinum in 1.0 M sulphuric and 0.1 M perchloric acids

TL;DR: The potential range for the formation of Pt(II) corresponds to that predicted on thermodynamic grounds for the reduction of PtO 2, and an unidentified species is produced during the oxidation of the platinum electrode.
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