Abstract

Cu-Mn alloy films are electrodeposited on Au substrates as precursor alloys for the synthesis of fine-structured nanoporous Cu structures. The alloys are deposited galvanostatically in a solution containing ammonium sulfate, (NH4)2SO4, which serves as a source of the ammine ligand that complexes with Cu, thereby decreasing the inherent standard reduction potential difference between Cu and Mn. The formation of the [Cu(NH3)n]2+ complex was confirmed by UV-Vis spectroscopic and voltammetric studies. Galvanostatic deposition at current densities ranging from 100 to 200 mA⋅cm−2 generally resulted in the formation of type I, crystalline coatings as revealed by scanning electron microscopy. Although the deposition current efficiency is (<30%) generally low, the atomic composition (determined by energy dispersive X-ray spectroscopy) of the deposited alloys range from 70–85 at% Mn, which is controlled by simply adjusting the ratio of the metal ion concentrations in the deposition bath. Anodic stripping characterization revealed a three-stage dissolution of the deposited alloys, which suggests control over the selective removal of Mn. The composition of the alloys obtained in the studies are ideal for electrochemical dealloying to form nanoporous Cu.

Highlights

  • Manganese (Mn) and its alloys have been used extensively in the metal industry as galvanic sacrificial coating protection for steel to prevent corrosion and degradation [1,2,3,4,5]

  • energy dispersive X-ray spectroscopy (EDS) was performed on three different areas of the working electrode (WE) and the result ported as average atomic percentages

  • Cu-Mn alloys were electrodeposited on Au substrates as precursor alloys for the synthesis of nanoporous Cu

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Summary

Introduction

Manganese (Mn) and its alloys have been used extensively in the metal industry as galvanic sacrificial coating protection for steel to prevent corrosion and degradation [1,2,3,4,5]. According to the Cu-Mn binary phase diagram, increasing the Cu content in the alloy (to approximately 18 atomic percent, at%) can prevent the deterioration of the Mn-rich α-phase that is generally unstable and exhibits similar properties as pure Mn coatings [5,16]. Mn-alloy coatings can be characterized into two categories, namely type I and type II The former has a crystalline morphology with regularly shaped grains while the latter is more compact and amorphous [4,5,17].

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