Arrays of ultra-thin selenium-doped zirconium-anodic-oxide nanorods as potential antibacterial coatings

Arrays of ultra-thin selenium-doped zirconium-anodic-oxide nanorods as potential antibacterial coatings

Článek WoS

Two characteristic types of extraordinarily thin upright-standing ZrO2-based nanorods self-aligned on a substrate, differing in diameters (20/30 nm), lengths (90/120 nm), and population densities (1.1/4.6 × 1010 cm−2), were synthesized via the porous-anodic-alumina (PAA)-assisted anodization of Zr in 1.5 M selenic acid followed by selective PAA dissolution. A needle-like shape was achieved due to the unique formation of zirconium anodic oxide in extremely thin nanopores that grow only in selenic acid. The SEM, XPS, and Raman spectroscopy analyses revealed that the nanorods feature a core/shell structure in which the core is stoichiometric amorphous ZrO2, and the shell is ∼6 nm thick hydroxylated zirconium dioxide ZrO2−x(OH)2x mixed with Al2O3. The core and shell incorporated electrolyte-derived selenate (SeO42−) ions, which replace up to 1% of the O2− ions in the nanorod surface layer. Besides, nanoparticles of elemental Se were deposited on the top of rods during anodic polarization. A model was developed for the cooperative ionic transport and electrochemical and solid-state reactions during the PAA-assisted growth of zirconium oxide in selenic acid. The two Se-doped top-decorated zirconium-oxide nanorod arrays were examined as potential antibacterial nanomaterials toward G-negative E. coli and G-positive S. aureus, using direct SEM observations of the bacteria–surface interfaces and carrying out the modified Japanese Industrial Standard test for antimicrobial activity and efficacy, JIS Z 2801. While specific differences in interaction with each type of bacteria were observed, both nanostructures caused a significant harmful synergetic effect on the bacteria, acting as non-metallic (Se) ion-releasing bactericidal coatings along with repellent and contact-killing activities arising from extraordinary needle-like nanoscale surface engineering.

Two characteristic types of extraordinarily thin upright-standing ZrO2-based nanorods self-aligned on a substrate, differing in diameters (20/30 nm), lengths (90/120 nm), and population densities (1.1/4.6 × 1010 cm−2), were synthesized via the porous-anodic-alumina (PAA)-assisted anodization of Zr in 1.5 M selenic acid followed by selective PAA dissolution. A needle-like shape was achieved due to the unique formation of zirconium anodic oxide in extremely thin nanopores that grow only in selenic acid. The SEM, XPS, and Raman spectroscopy analyses revealed that the nanorods feature a core/shell structure in which the core is stoichiometric amorphous ZrO2, and the shell is ∼6 nm thick hydroxylated zirconium dioxide ZrO2−x(OH)2x mixed with Al2O3. The core and shell incorporated electrolyte-derived selenate (SeO42−) ions, which replace up to 1% of the O2− ions in the nanorod surface layer. Besides, nanoparticles of elemental Se were deposited on the top of rods during anodic polarization. A model was developed for the cooperative ionic transport and electrochemical and solid-state reactions during the PAA-assisted growth of zirconium oxide in selenic acid. The two Se-doped top-decorated zirconium-oxide nanorod arrays were examined as potential antibacterial nanomaterials toward G-negative E. coli and G-positive S. aureus, using direct SEM observations of the bacteria–surface interfaces and carrying out the modified Japanese Industrial Standard test for antimicrobial activity and efficacy, JIS Z 2801. While specific differences in interaction with each type of bacteria were observed, both nanostructures caused a significant harmful synergetic effect on the bacteria, acting as non-metallic (Se) ion-releasing bactericidal coatings along with repellent and contact-killing activities arising from extraordinary needle-like nanoscale surface engineering.

anodizing, zirconium oxide, biomedical application

anodizing, zirconium oxide, biomedical application

KAMNEV, K.; BENDOVÁ, M.; FOHLEROVÁ, Z.; FIALOVÁ, T.; MARTYNIUK, O.; PRÁŠEK, J.; ČÍHALOVÁ, K.; MOZALEV, A.

17.01.2025

ROYAL SOC CHEMISTRY

THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND

2052-1537

Materials Chemistry Frontiers

9

5

Spojené království Velké Británie a Severního Irska

866

883

18

https://pubs.rsc.org/en/content/articlelanding/2025/qm/d4qm01081g

http://hdl.handle.net/11012/255380

d4qm01081g