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In the present work, the magnetron sputtering technique was used to prepare new catalysts of formic acid electrooxidation based on TiO 2 nanotubes decorated with Pt (platinum), Pd (palladium) or Pd + Pt nanoparticles. TiO 2 nanotubes (TiO 2 NTs) with strictly defined geometry were produced by anodization of Ti foil and Ti mesh in a mixture of glycerol and water with ammonium fluoride electrolyte. The above mentioned catalytically active metal nanoparticles (NPs) were located mainly on the top of the TiO 2 NTs, forming 'rings' and agglomerates. A part of metal nanoparticles decorated also TiO 2 NTs walls, thus providing sufficient electronic conductivity for electron transportation between the metal nanoparticle rings and Ti current collector. The electrocatalytic activity of the TiO 2 NTs/Ti foil, decorated by Pt, Pd and/or Pd + Pt NPs was investigated by cyclic voltammetry (CV) and new Pd/TiO 2 NTs/Ti mesh catalyst was additionally tested in a direct formic acid fuel cell (DFAFC). The results so obtained were compared with commercial catalyst-Pd/Vulcan. CV tests have shown for carbon supported catalysts, that the activity of TiO 2 NTs decorated with Pd was considerably higher than that one decorated with Pt. Moreover, for TiO 2 NTs supported Pd catalyst specific activity (per mg of metal) was higher than that for well dispersed carbon supported commercial catalyst. The tests at DFAFC have revealed also that the maximum of specific power for 0.2 Pd/TiO 2 catalyst was 70% higher than that of the commercial one, Pd/Vulcan. Morphological features, and/or peculiarities, as well as surface composition of the resulting catalysts have been studied by scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), and chemical surface analytical methods (X-ray photoelectron spectroscopy-XPS; Auger electron spectroscopy-AES)., Competing Interests: The authors declare no conflict of interest.

In this work we show that ordered freestanding titanium oxide nanotubes (TiO 2 NT) may be used as substrates for the simple and efficient immobilization of anisotropic plasmonic nanoparticles. This is important because anisotropic plasmonic nanostructures usually give greater spectral enhancement than spherical nanoparticles. The size of the pores in a layer of titanium oxide nanotubes can be easily fitted to the size of many silver plasmonic nanoparticles highly active in SERS (surface-enhanced Raman scattering) spectroscopy (for example, silver nanocubes with an edge length of ca. 45 nm), and hence, the plasmonic nanoparticles deposited can be strongly anchored in such a titanium oxide substrate. The tubular morphology of the TiO 2 substrate used allows a specific arrangement of the silver plasmonic nanoparticles that may create many so-called SERS hot spots. The SERS activity of a layer of cubic Ag nanoparticles (AgCNPs) deposited on a tubular TiO 2 substrate (AgCNPs@TiO 2 NT) is about eight times higher than that of the standard electrochemically nanostructured surface of a silver electrode (produced by oxidation reduction cycling). Furthermore, a super hydrophilic character of the TiO 2 nanotubes surface allows for a uniform distribution of AgCNPs, which are deposited from an aqueous suspension. The new AgCNPs@TiO 2 NT hybrid layer ensures a good reproducibility of SERS measurements and exhibits a higher temporal stability of the achievable total SERS enhancement factor-one that is far better than standard SERS silver substrates. To characterize the morphology and chemical composition of such evidently improved SERS platforms thus received, we applied microscopic techniques (SEM, and scanning transmission electron microscopy (STEM)) and surface analytical techniques (Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS)).

Titanium oxide nanotube layers with silver and zinc nanoparticles are attracting increasing attention in the design of bone and dental implants due to their antimicrobial potential and their ability to control host cell adhesion, growth, and differentiation. However, recent reports indicate that the etiology of dental infections is more complex than has been previously considered. Therefore, the antimicrobial potential of dental implants should be evaluated against at least several different microorganisms cooperating in human mouth colonization. In this study, Ag and Zn nanoparticles incorporated into titanium oxide nanotubular layers were studied with regard to how they affect Candida albicans, Candida parapsilosis, and Streptococcus mutans. Layers of titanium oxide nanotubes with an average diameter of 110 nm were fabricated by electrochemical anodization, annealed at 650 °C, and modified with approx. 5 wt % Ag or Zn nanoparticles. The surfaces were examined with the scanning electron microscopy-energy dispersive X-ray analysis, scanning transmission electron microscopy, and X-ray photoelectron spectroscopy techniques and subjected to evaluation of microbial-killing and microbial adhesion-inhibiting potency. In a 1.5 h long adhesion test, the samples were found more effective toward yeast strains than toward S. mutans. In a release-killing test, the microorganisms were almost completely eliminated by the samples, either within 3 h of contact (for S. mutans) or 24 h of contact (for both yeast strains). Although further improvement is advisable, it seems that Ag and Zn nanoparticles incorporated into TiO 2 nanotubular surfaces provide a powerful tool for reducing the incidence of bone implant infections. Their high bidirectional activity (against both Candida species and S. mutans) makes the layers tested particularly promising for the design of dental implants.