Published March 2022 | Version v1
Journal article

Titanium anodization in deep eutectic solvents: The effect of anodizing time on the morphology and structure of anodic layers

  • 1. Group of Surface Technology, Department of Advanced Material Technologies, Wrocław University of Science and Technology, Wybrzeże Wyspiańskiego 27, Wrocław 50-370 (Poland)
  • 2. Materials Research Laboratory, Faculty of Mechanical Engineering, Silesian University of Technology, Konarskiego 18A, Gliwice 44-100 (Poland)

Description

Highlights: • DES as the environment for Grade 2 titanium anodizing process. • Potentiostatic anodic formation of compact nanometric TiO2 layer. • Time-controlled growth of TiO2 layer thickness. • Transition from amorphous to nanocrystalline structure with increasing time. Deep eutectic solvents (DES) are successfully used as green solvents for electrochemical polishing of titanium. The tests performed showed that they can also be used for the production of nanometric TiO2 layers on Grade 2 titanium with thickness and crystallinity controlled by the anodizing time. Anodic polarization at 60 °C in choline dihydrogencitrate salt : oxalic acid DES allows to obtain amorphous TiO2 layer with a thickness of 5–11 nm in just a few seconds. Extending this time to 30 s causes, apart from increasing layer thickness, a distinct development of its surface. In the layer formed during the 20 min of polarization, nanosized crystalline domains begin to dominate, and the thickness of the TiO2 layer increases to approx. 30 nm. The process accompanying titanium anodizing is the incorporation of small amounts of "organic" carbon, most likely DES residues, into the structure of TiO2 layers.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2021.151892

Additional details

Identifiers

DOI
10.1016/j.apsusc.2021.151892;
PII
S0169433221029342;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
577
Journal Page Range
vp.
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2021 The Author(s). Published by Elsevier B.V.