Model of nickel electrodeposition from acidic medium
Identifieur interne : 000416 ( France/Analysis ); précédent : 000415; suivant : 000417Model of nickel electrodeposition from acidic medium
Auteurs : F. Lantelme [France] ; A. Seghiouer [France] ; A. Derja [Maroc]Source :
- Journal of applied electrochemistry [ 0021-891X ] ; 1998.
Descripteurs français
- Pascal (Inist)
- Etude expérimentale, Modélisation, Réaction électrochimique, Dépôt électrolytique, Codépôt, Nickel, Nickel II Hydroxyde, Electrode disque tournant, Carbone, Etat vitreux, Effet milieu, pH, Chronoampérométrie, Structure surface, Microscopie électronique balayage, Morphologie, Solution aqueuse, Solution acide.
- Wicri :
English descriptors
- KwdEn :
Abstract
A step-wise computer model is presented for simultaneous deposition of nickel and nickel hydroxide in aqueous solutions. In acidic solutions (pH ≃ 1), the potentiostatic current-time transient response on glassy carbon or titanium was analysed with respect to nucleation and radial growth mechanism. pH changes influence the current-time response greatly. A marked maximum in the current transient appears for slightly acidic solutions (pH > 4.5) and a consecutive decrease in the deposition current density at long times is obtained. This behaviour is attributed to early precipitation of nickel hydroxide due to a local pH increase at the cathode surface.
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PascalFrancis, to step Corpus: 000472
- to stream PascalFrancis, to step Curation: 000595
- to stream PascalFrancis, to step Checkpoint: 000487
- to stream Main, to step Merge: 000D86
- to stream Main, to step Curation: 000D40
- to stream Main, to step Exploration: 000D40
- to stream France, to step Extraction: 000416
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Pascal:99-0047431Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acidic solution</term>
<term>Aqueous solution</term>
<term>Carbon</term>
<term>Chronoamperometry</term>
<term>Codeposition</term>
<term>Electrochemical reaction</term>
<term>Electrodeposition</term>
<term>Experimental study</term>
<term>Glassy state</term>
<term>Medium effect</term>
<term>Modeling</term>
<term>Morphology</term>
<term>Nickel</term>
<term>Nickel II Hydroxides</term>
<term>Rotating disk electrode</term>
<term>Scanning electron microscopy</term>
<term>Surface structure</term>
<term>pH</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Etude expérimentale</term>
<term>Modélisation</term>
<term>Réaction électrochimique</term>
<term>Dépôt électrolytique</term>
<term>Codépôt</term>
<term>Nickel</term>
<term>Nickel II Hydroxyde</term>
<term>Electrode disque tournant</term>
<term>Carbone</term>
<term>Etat vitreux</term>
<term>Effet milieu</term>
<term>pH</term>
<term>Chronoampérométrie</term>
<term>Structure surface</term>
<term>Microscopie électronique balayage</term>
<term>Morphologie</term>
<term>Solution aqueuse</term>
<term>Solution acide</term>
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<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Nickel</term>
<term>Carbone</term>
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<front><div type="abstract" xml:lang="en">A step-wise computer model is presented for simultaneous deposition of nickel and nickel hydroxide in aqueous solutions. In acidic solutions (pH ≃ 1), the potentiostatic current-time transient response on glassy carbon or titanium was analysed with respect to nucleation and radial growth mechanism. pH changes influence the current-time response greatly. A marked maximum in the current transient appears for slightly acidic solutions (pH > 4.5) and a consecutive decrease in the deposition current density at long times is obtained. This behaviour is attributed to early precipitation of nickel hydroxide due to a local pH increase at the cathode surface.</div>
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