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Metallic implants have been successfully used in medicine for the past 60–70 years. Historically, implants were designed only as mechanical devices, whereas the biological aspects of their application were beyond the researchers’ interest. The improvement of living conditions and the increase of the average life span have changed the situation. The clinical requirements for medical implants rise up substantially. Presently, it seems impossible to imagine the use of metallic implants in the human body without preliminary surface modification to modulate the interaction between the surrounding biological environment and the implant. The review highlights the most recent advances in the field of functional coatings formed on implants by the plasma electrolytic oxidation technology. Special attention is dedicated to the principles of surface modification of the commercially pure titanium, titanium nickelide, and Mg-Mn-Ce magnesium alloy. The advantages and disadvantages of the method and the characteristics of these materials are discussed from this point of view. Some aspects of this review are aimed at corrosion protection of implants with application of polymer materials.

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Hafnium-doped titania (Hf/Ti = 0.01; 0.03; 0.05) had been facilely synthesized via a template sol–gel method on carbon fibre. Physico-chemical properties of the as-synthesized materials were characterized by X-ray diffraction, Raman spectroscopy, scanning electron microscopy, energy-dispersive X-ray analysis, scanning transmission electron microscopy, X-ray photoelectron spectroscopy, thermogravimetry analysis and Brunauer–Emmett–Teller measurements. It was confirmed that Hf4+ substitute in the Ti4+ sites, forming Ti1–xHfxO2 (x = 0.01; 0.03; 0.05) solid solutions with an anatase crystal structure. The Ti1–xHfxO2 materials are hollow microtubes (length of 10–100 µm, outer diameter of 1–5 µm) composed of nanoparticles (average size of 15–20 nm) with a surface area of 80–90 m2 g–1 and pore volume of 0.294–0.372 cm3 g–1. The effect of Hf ion incorporation on the electrochemical behaviour of anatase TiO2 in the Li-ion battery anode was investigated by galvanostatic charge/discharge and electrochemical impedance spectroscopy. It was established that Ti0.95Hf0.05O2 shows significantly higher reversibility (154.2 mAh g–1) after 35-fold cycling at a C/10 rate in comparison with undoped titania (55.9 mAh g–1). The better performance offered by Hf4+ substitution of the Ti4+ into anatase TiO2 mainly results from a more open crystal structure, which has been achieved via the difference in ionic radius values of Ti4+ (0.604 Å) and Hf4+ (0.71 Å). The obtained results are in good accord with those for anatase TiO2 doped with Zr4+ (0.72 Å), published earlier. Furthermore, improved electrical conductivity of Hf-doped anatase TiO2 materials owing to charge redistribution in the lattice and enhanced interfacial lithium storage owing to increased surface area directly depending on the Hf/Ti atomic ratio have a beneficial effect on electrochemical properties.