介电谱
电化学
无机化学
沉积(地质)
极化(电化学)
次磷酸钠
次磷酸
阴极保护
电镀
动力学
化学
电极
物理化学
图层(电子)
古生物学
物理
有机化学
量子力学
沉积物
生物
作者
Alberto Pires Ordine,S.L. Díaz,Isabel Margarit,Oswaldo E. Barcia,O.R. Mattos
标识
DOI:10.1016/j.electacta.2005.02.129
摘要
Abstract The kinetics of P incorporation during Ni–P electrodeposition was investigated by means of interfacial pH measurements, cathodic polarization curves and electrochemical impedance spectroscopy. This process is strongly affected by solution pH. A buffering effect provided by sodium hypophosphite in the solution was observed at pH 1.5. By contrast, at pH 4.0, this effect was not observed and an increase in the degree of alkalination at the interface was verified. At pH 1.5, Ni 2+ reduction was strongly disfavored during Ni–P deposition. The impedance measurements indicated that the mechanism of Ni deposition was modified by the presence of NaH 2 PO 2 ·H 2 O in the solution. The characteristic time constants for the individual cathodic processes, H + , Ni 2+ and NaH 2 PO 2 reduction, could be identified during Ni–P electrodeposition. Moreover, at pH 4.0, Ni–P deposition occurs by means of a different mechanism than that observed at pH 1.5. These findings cannot be described by any of the models for Ni–P electrodeposition found in literature.
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