Inorganic nanomaterials able to generate reactive oxygen species (ROS) are promising components for modern medical applications. Activated by near-infrared light, up-converting b-NaYF 4 doped with Er 3+ -Yb 3+ and Tm 3+ -Yb 3+ pair ions nanoparticles (UCNPs), have a wide range of applications in biological imaging as compared to traditional reagents excited by ultra-violet or visible light. We analysed the green-red and the blue-red luminescence to explain the mechanism of the upconversion depended on the surface condition. The influence of SiO 2 coating on the cytotoxicity of the as-produced UCNPs towards HeLa cancer cells was reported. We demonstrated a possibility of a direct UCNPs application to photodynamic therapy, without need to attach additional molecules to their surface. The presence of Tm 3+ -Yb 3+ pair ions, thus ROS generation capability, renders the SiO 2 shell coated nanoparticles to become potentially useful theranostic agent.

In this study Pt, Re, and SnO2 nanoparticles (NPs) were combined in a controlled manner into binary and ternary combinations for a possible application for ethanol oxidation. For this purpose, zeta potentials as a function of the pH of the individual NPs solutions were measured. In order to successfully combine the NPs into Pt/SnO2 and Re/SnO2 NPs, the solutions were mixed together at a pH guaranteeing opposite zeta potentials of the metal and oxide NPs. The individually synthesized NPs and their binary/ternary combinations were characterized by Fourier transform infrared spectroscopy (FTIR) and scanning transmission electron microscopy (STEM) combined with energy dispersive X-ray spectroscopy (EDS) analysis. FTIR and XPS spectroscopy showed that the individually synthesized Pt and Re NPs are metallic and the Sn component was oxidized to SnO2. STEM showed that all NPs are well crystallized and the sizes of the Pt, Re, and SnO2 NPs were 2.2, 1.0, and 3.4 nm, respectively. Moreover, EDS analysis confirmed the successful formation of binary Pt/SnO2 and Re/SnO2 NP, as well as ternary Pt/Re/SnO2 NP combinations. This study shows that by controlling the zeta potential of individual metal and oxide NPs, it is possible to assemble them into binary and ternary combinations. Graphical abstractᅟ Electronic supplementary materialThe online version of this article (10.1007/s11051-018-4244-0) contains supplementary material, which is available to authorized users.

Hollow multimetallic PtNiSn nanoparticles (NPs) were formed from solid Ni-core/Pt-frame NPs by galvanic replacement reaction (GRR) of Ni by Sn.

Pt-based nanoframes are one of the most promising catalysts for ethanol oxidation reaction in direct ethanol fuel cells. It is important to understand the mechanisms responsible for creating these hollow nanoframe-based catalysts. Herein, for the first time, Pt-skin PtRhNi rhombic dodecahedral nanoframes were decorated with small SnO 2 nanoparticles and were used as an efficient catalyst for the ethanol oxidation reaction. Moreover, by combining the ex situ scanning transmission electron microscopy and energy-dispersive X-ray spectroscopy observations at various stages of synthesis, along with density functional theory calculations, it was possible to track the synthesis route of solid rhombic dodecahedral PtRhNi nanoparticles, which are the precursors of PtRhNi nanoframes. After the chemical etching of the Ni core from solid PtRhNi nanoparticles, the obtained nanoframes were decorated with SnO 2 nanoparticles. The resulting SnO 2 @PtRhNi heteroaggregates were deposited on highsurface-area carbon and electrochemically tested, showing a 6-fold higher mass activity and 10-fold higher specific activity toward ethanol oxidation reaction than commercially available Pt catalysts.