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The formation and dissolution of an electrochemical oxide film of up to a monolayer thickness on gold

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This article is published in Journal of Electroanalytical Chemistry.The article was published on 1974-03-10. It has received 33 citations till now. The article focuses on the topics: Monolayer & Oxide.

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The potentiodynamic behaviour of iron in alkaline solutions

TL;DR: In this paper, the potentiodynamic behavior of iron in alkaline solutions under carefully controlled perturbation conditions reveals that the overall electrochemical process is more involved than was thought earlier, and the electrochemical characteristics of the systems are explained through a series of successive conjugated redox couples principally involving Fe(OH), Fe( OH) 2 and FeOOH as limiting stoichiometric species.
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Electrochemical characterization of mild steel in alkaline solutions simulating concrete environment

TL;DR: In this article, the electrochemical behavior of B450C mild steel was studied in saturated Ca(OH)2 solution by cyclic voltammetry, and the influence that time has on the passive film growth was then investigated by means of anodic polarization and electrochemical impedance spectroscopy.
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Transient changes of intermediate species formed during the electrooxidation and surface electroreduction of gold within a monolayer thickness range

TL;DR: In this article, the species formed during the anodic oxidation and electroreduction of a gold electrode surface within the range of a monolayer thickness is given by means of triangular potential sweeps run under different experimental conditions.
References
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The real condition of electrochemically oxidized platinum surfaces

TL;DR: In this article, the problem of the initial stages of Pt surface oxidation below a monolayer of electrosorbed OH (1 e per Pt atom), even on single crystal faces, is examined.
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The effect of strong acid on the reactions of hydrogen and oxygen on the noble metals. A study using cyclic voltammetry and a new teflon electrode holder

TL;DR: In this article, the voltammograms of Pt, Pd, Rh, Ir and Au are compared in sulphuric acid for concentrations of 1.5 M. The difference between the anion adsorption (Cl− and SO42−) and strong sulphURic acid on the shapes of the voltamograms is demonstrated.
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