Electrochemical Deposition of Al-Ti Alloys from Equimolar AlCl₃ + NaCl Containing Electrochemically Dissolved Titanium

Abstract

Al-Ti alloys were electrodeposited from equimolar chloroaluminate molten salts containing up to 0.1 M of titanium ions, which were added to the electrolyte by potentiostatic dissolution of metallic Ti. Titanium dissolution and titanium and aluminium deposition were investigated by linear sweep voltammetry and chronoamperometry at 200 and 300 °C. Working electrodes used were titanium and glassy carbon. The voltammograms on Ti obtained in the electrolyte without added Ti ions indicated titanium deposition and dissolution proceeding in three reversible steps: Ti4+ ⇄ Ti3+, Ti3+ ⇄ Ti2+ and Ti2+ ⇄ Ti. The voltammograms recorded with glassy carbon in the electrolyte containing added titanium ions did not always clearly register all of the three processes. However, peak currents, which were characteristics of Al, Ti and Al-Ti alloy deposition and dissolution, were evident in voltammograms on both working electrodes used. A constant potential electrodeposition regime was used to obtain deposits on the glassy carbon working electrode. The obtained deposits were characterized by SEM, energy-dispersive spectrometry and XRD. In the deposits on the glassy carbon electrode, the analysis identified an Al and AlTi3 alloy formed at 200 °C and an Al2Ti and Al3Ti alloy obtained at 300 °C.

Keywords

• al-ti alloy
• electrochemical co-deposition
• chloroaluminate melt
• xrd