For the first time, plasma electrolytic oxidation (PEO) coatings are fabricated on tantalum in NaCl electrolytes. The morphology of the resulting coatings is strongly dependent on the electrolyte concentration. In 0.01 M NaCl, the coating formed for 600 s is non-uniform, showing a nodular surface with a thick sample edge (∼100 μm) and extremely thin center area. In contrast, coatings are uniform in 0.1 and 1 M NaCl. The coating exhibits a grooved surface morphology and a thickness of ∼42 μm in 0.1 M NaCl. However, the morphology changed into round pores and the thickness is reduced to ∼25 μm in 1 M NaCl. XRD confirms that all coatings consist of crystalline Ta2O5. Electrochemical tests indicate that the PEO treatment significantly improves the corrosion resistance of tantalum in simulated body fluid (SBF). The coating formed in 0.1 M NaCl exhibits the lowest corrosion current density (iCORR) of 6.04 × 10−9 A cm−2, which is two-order lower than that of bare tantalum (iCORR = 1.77 × 10−7 A cm−2). Mott-Schottky analyses indicate that all coatings are n-type semiconductor with donor densities between 5.38 × 1017 cm−3 and 3.64 × 1017 cm−3. All coatings are hydrophilic, showing contact angles between 33.4° ± 6.5° and 64.1° ± 4.8°. The 1 M coating shows the highest bonding strength (> ∼7.81 ± 0.25 MPa). Cell biocompatibility of the coatings was assessed using L929 mouse fibroblasts and the CCK-8 assay. In contrast to the round morphology on bare tantalum, the cells on the oxidized surfaces displayed a spindle-like morphology, demonstrating favorable biointerface characteristics. Meanwhile, the cell relative metabolic activity of all coatings on day 7 was approximately 23–25 times higher than that of the substrate. Finally, comparative study on titanium confirms that the formation of PEO coatings on tantalum in NaCl electrolytes is a unique phenomenon among valve metals. This study provides a new way to prepare biocompatible coatings on tantalum and deeper insights into the PEO coating formation mechanisms.
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