Abstract

Electrochemical behaviour of pure titanium was studied in KOH-based media over a large voltage range (0-700V) in order to understand the micro-arc phenomenon occurrence, leading to the formation of a “ceramic-like” oxide layer. The influence of various KOH concentrations in the electrolytic bath (from 0.01 to 0.2M) was investigated on titanium substrate by a potentiodynamic scan. Whatever the concentration, the electrochemical behaviour of titanium in KOH media can be described in three steps according to voltage: i) a “conventional anodizing” step controlled by the solid-state diffusion of O2− and Ti4+ ions under the electric field effect, ii) a voltage range during which the micro-arc phenomenon occurs, named “micro-arc region”, iii) a “sharp current rise” induced by the increase of oxide conductivity. After anodizing in galvanostatic conditions, XRD and EDS analyses combined with SEM observations show that all samples have similar morphology with a dense internal layer and a porous external one, constituted by titanium dioxide under anatase and rutile crystallized forms. The electrochemical behaviour of anodized layers was investigated by electrochemical impedance spectroscopy measurements. A Mott-Schottky analysis reveals a n-type semi-conducting behaviour of the oxide layers with a very high donor concentration between 1022 and 1023cm−3.

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