Diffusion doping of cobalt in rod-shape anatase TiO\u3csub\u3e2\u3c/sub\u3e nanocrystals leads to antiferromagnetism†

Cobalt(II) ions were adsorbed to the surface of rod-shape anatase TiO2 nanocrystals and subsequently heated to promote ion diffusion into the nanocrystal. After removal of any remaining surface bound cobalt, a sample consisting of strictly cobalt-doped TiO2 was obtained and characterized with powder Xray diffraction, transmission electron microscopy, UV-visible spectroscopy, fluorescence spectroscopy, X-ray photoelectron spectroscopy, SQUID magnetometry, and inductively-coupled plasma atomic emission spectroscopy. The nanocrystal morphology was unchanged in the process and no new crystal phases were detected. The concentration of cobalt in the doped samples linearly correlates with the initial loading of cobalt(II) ions on the nanocrystal surface. Thin films of the cobalt doped TiO2 nanocrystals were prepared on indium-tin oxide coated glass substrate, and the electrical conductivity increased with the concentration of doped cobalt. Magnetic measurements of the cobalt-doped TiO2 nanocrystals reveal paramagnetic behavior at room temperature, and antiferromagnetic interactions between Co ions at low temperatures. Antiferromagnetism is atypical for cobalt-doped TiO2 nanocrystals, and is proposed to arise from interstitial doping that may be favored by the diffusional doping mechanism

Ligand Controlled Morphology Evolution of Active Intermediates for the Syntheses of Gold Nanostars

Gold nanostars have unique plasmonic properties that are related to the highly branched nanostructures. However, it is challenging to precisely control these branches. Here we studied the reaction kinetics on the seed-mediated growth process of gold nanostars using <i>in situ</i> UV–vis spectroscopy. The impact of hydroquinone ligands on the formation and evolution of active intermediates was systematically explored. In addition, we improved the classical seed-mediated method to achieve a much better control on the final morphology of gold nanostars by a sudden addition of a high concentration ligand solution. Our method can significantly advance the syntheses of gold nanostars and provide numerous opportunities to prepare nanomaterials with unique morphology and plasmonic properties

SnS2/TiO2 Nanocomposites for Hydrogen Production and Photodegradation under Extended Solar Irradiation

Earth–abundant transition metal chalcogenide materials are of great research interest for energy production and environmental remediation, as they exhibit better photocatalytic activity due to their suitable electronic and optical properties. This study focuses on the photocatalytic activity of flower-like SnS2 nanoparticles (composed of nanosheet subunits) embedded in TiO2 synthesized by a facile hydrothermal method. The materials were characterized using different techniques, and their photocatalytic activity was assessed for hydrogen evolution reaction and the degradation of methylene blue. Among the catalysts studied, 10 wt. % of SnS2 loaded TiO2 nanocomposite shows an optimum hydrogen evolution rate of 195.55 µmolg−1, whereas 15 wt. % loading of SnS2 on TiO2 exhibits better performance against the degradation of methylene blue (MB) with the rate constant of 4.415 × 10−4 s−1 under solar simulated irradiation. The improved performance of these materials can be attributed to the effective photo-induced charge transfer and reduced recombination, which make these nanocomposite materials promising candidates for the development of high-performance next-generation photocatalyst materials. Further, scavenging experiments were carried out to confirm the reactive oxygen species (ROS) involved in the photocatalytic degradation. It can be observed that there was a 78% reduction in the rate of degradation when IPA was used as the scavenger, whereas around 95% reduction was attained while N2 was used as the scavenger. Notably, very low degradation (<5%) was attained when the dye alone was directly under solar irradiation. These results further validate that the •OH radical and the superoxide radicals can be acknowledged for the degradation mechanism of MB, and the enhancement of degradation efficiency may be due to the combined effect of in situ dye sensitization during the catalysis and the impregnation of low bandgap materials on TiO

SnS2/TiO2 Nanocomposites for Hydrogen Production and Photodegradation under Extended Solar Irradiation

Earth–abundant transition metal chalcogenide materials are of great research interest for energy production and environmental remediation, as they exhibit better photocatalytic activity due to their suitable electronic and optical properties. This study focuses on the photocatalytic activity of flower-like SnS2 nanoparticles (composed of nanosheet subunits) embedded in TiO2 synthesized by a facile hydrothermal method. The materials were characterized using different techniques, and their photocatalytic activity was assessed for hydrogen evolution reaction and the degradation of methylene blue. Among the catalysts studied, 10 wt. % of SnS2 loaded TiO2 nanocomposite shows an optimum hydrogen evolution rate of 195.55 µmolg−1, whereas 15 wt. % loading of SnS2 on TiO2 exhibits better performance against the degradation of methylene blue (MB) with the rate constant of 4.415 × 10−4 s−1 under solar simulated irradiation. The improved performance of these materials can be attributed to the effective photo-induced charge transfer and reduced recombination, which make these nanocomposite materials promising candidates for the development of high-performance next-generation photocatalyst materials. Further, scavenging experiments were carried out to confirm the reactive oxygen species (ROS) involved in the photocatalytic degradation. It can be observed that there was a 78% reduction in the rate of degradation when IPA was used as the scavenger, whereas around 95% reduction was attained while N2 was used as the scavenger. Notably, very low degradation (&lt;5%) was attained when the dye alone was directly under solar irradiation. These results further validate that the •OH radical and the superoxide radicals can be acknowledged for the degradation mechanism of MB, and the enhancement of degradation efficiency may be due to the combined effect of in situ dye sensitization during the catalysis and the impregnation of low bandgap materials on TiO2

Stable Inks Containing Upconverting Nanoparticles Based on an Oil-in-Water Nanoemulsion

An oil-in-water nanoemulsion capable of dispersing upconverting nanoparticles (UCNPs) for 7 months was investigated. Negative staining transmission electron microscopy shows that the UCNPs reside in the oil phase of the nanoemulsion. Dynamic light scattering measurements indicate that the majority of the oil volume is contained in droplets less than 1 μm in diameter. The system studied could be used to inkjet print UCNPs at least 7 months after the ink was first formulated. Nanoemulsion stability was tested in the short term, over 11 days, using an ink stability test developed for this research. It was found that after an initial loss of UCNPs, the majority of the UCNPs remained well-dispersed in solution. The UCNP dispersion was stable for longer periods under storage at 333 K compared to storage at 277 K