Abstract
The influence of glycine on the iron phosphorous alloy electrodeposition was investigated by electrochemical quartz microbalance (EQMB), in-situ external reflection FTIR spectroscopy, and electrochemical impedance spectroscopy (EIS) measurements. An increase of glycine concentration leads to a decrease of the iron-phosphorous alloy electrodeposition rate and an increase of hydrogen evolution. Strong adsorption of glycine species, such as H2(gly)+, H(gly)± or/and Fe(gly)+, have been observed during the hydrogen evolution and the Fe-P deposition reaction. Due to the concurrent hydrogen evolution the pH attains higher values at the interface than in the electrolyte bulk (pH2.5). The formation of adsorbed Fe(gly)+ and of the chelate complex Fe(gly)2 in solution avoids the precipitation of Fe(OH)2 in the pH range between 2.5 and ca. 7 at the interface. The phosphorous content of the iron phosphorous alloy deposit increases with the glycine concentration. This is due to a lower deposition rate of iron caused by the adsorption of Fe(gly)+, while the hypophosphite reduction rate to phosphorous increases.
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