2011
DOI: 10.1016/j.electacta.2011.06.079
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Electrodeposition of CoNiMo thin films using glycine as additive: anomalous and induced codeposition

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Cited by 33 publications
(11 citation statements)
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“…Nevertheless, due to hydrogen evolution competing with metal deposition, the pH in the direct vicinity of the electrode may be significantly higher than in the bulk solution. This might promote formation of cobalt and nickel complexes with the anionic glycine species resulting in [CoGly 3 ] and [NiGly 3 ] (), with their reversible potentials closer to EC than [NiGly 3 ]2+. Furthermore, formation of the cobalt complex occurs faster than the nickel complex (), making less glycine available for complexation of nickel with glycine.…”
Section: Resultsmentioning
confidence: 99%
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“…Nevertheless, due to hydrogen evolution competing with metal deposition, the pH in the direct vicinity of the electrode may be significantly higher than in the bulk solution. This might promote formation of cobalt and nickel complexes with the anionic glycine species resulting in [CoGly 3 ] and [NiGly 3 ] (), with their reversible potentials closer to EC than [NiGly 3 ]2+. Furthermore, formation of the cobalt complex occurs faster than the nickel complex (), making less glycine available for complexation of nickel with glycine.…”
Section: Resultsmentioning
confidence: 99%
“…This might promote formation of cobalt and nickel complexes with the anionic glycine species resulting in [CoGly 3 ] and [NiGly 3 ] (), with their reversible potentials closer to EC than [NiGly 3 ]2+. Furthermore, formation of the cobalt complex occurs faster than the nickel complex (), making less glycine available for complexation of nickel with glycine. Comparing the calculated reversible potentials to the crossover potential, it might be concluded that EC results from combined reduction of non‐complexed metal ion species and complexes with glycine in the anionic form.…”
Section: Resultsmentioning
confidence: 99%
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“…The predominant Ni‐Gly complexes according to Esteves et al are [NiGly] + and [Ni(Gly) 2 ], in which the glycine ligands in the direct vicinity of the cathode are in the form of normalH2normalNnormalCH2normalCOO, because hydrogen evolution as a side reaction of electroplating is accompanied by a local increase of pH value. Ortiz–Aparicio et al report [CoGly] + and [Zn(Gly) 2 ] to be the major species of Co‐Gly and Zn‐Gly complexes.…”
Section: Resultsmentioning
confidence: 99%
“…In order to improve the efficiency of the electrodeposition process and the structure of the obtained Co-W deposits organic additives, such as saccharin, thiourea, methacrylate, glycine can be used in the electrolyte. 42 Recently, glycine-based solutions are of interest because it is a non-toxic complexing agent, which stabilizes the pH close to the electrode surface in both alkaline and acidic electrolytes, 43,44 although the side reaction cannot be completely eliminated. Thus, the management of the hydrogen evolution side reaction can be problematic when translating thin film deposition parameters for Co-W alloys to nanometer architectures via templating methods.…”
Section: -38mentioning
confidence: 99%