Synthesis of PtNi Nanoparticles to Accelerate the Oxygen Reduction Reaction.

We report the synthesis of core-shell Ni-Pt nanoparticles (NPs) with varying degrees of crystallographic facets and surface layers rich in Pt via a seed-mediated thermolytic approach. Mixtures of different surfactants used during synthesis resulted in preferential surface passivation, which in turn dictated the size, chemical composition, and geometric evolution of these PtNi NPs. Electrochemical investigations of these pristine core-shell Ni-Pt structures in the oxygen reduction reaction (ORR) show that their catalytic functionalities outperform the commercial Pt/C reference catalyst. The enhanced electrocatalytic ORR performances of these Pt-based PtNi NPs are correlated with the weakened oxygen binding strength or surface-adsorbed hydroxyl (OH) species on active Pt surface sites induced by the downshift of the d-band center as a result of compressive strain effects. Our studies offer a robust synthetic approach for the development of core-shell nanostructures for enhanced ORR catalysis.

Catalyst Design: Counter Anion Effect on Ni Nanocatalysts Anchored on Hollow Carbon Spheres.

Herein, the influence of the counter anion on the structural properties of hollow carbon spheres (HCS) support was investigated by varying the nickel metal precursor salts applied. TEM and SEM micrographs revealed the dimensional dependence of the HCS shell on the Ni precursor salt, as evidenced by thick (~42 nm) and thin (~23 nm) shells for the acetate and chloride-based salts, respectively. Importantly, the effect of the precursor salt on the textural properties of the HCS nanosupports (~565 m2/gNi(acet)) and ~607 m2/gNiCl), influenced the growth of the Ni nanoparticles, viz for the acetate-(ca 6.4 nm)- and chloride (ca 12 nm)-based salts, respectively. Further, XRD and PDF analysis showed the dependence of the reduction mechanism relating to nickel and the interaction of the nickel-carbon support on the type of counter anion used. Despite the well-known significance of the counter anion on the size and crystallinity of Ni nanoparticles, little is known about the influence of such counter anions on the physicochemical properties of the carbon support. Through this study, we highlight the importance of the choice of the Ni-salt on the size of Ni in Ni-carbon-based nanocatalysts.

Synthesis and characterization of Y3+-doped TiO2 nanocomposites for photocatalytic applications.

The TiO(2).[Y(2)O(3)](x) (x = 0.1-0.4) nanocomposites (NCs) with an average particle size of 74 nm were prepared by the method of chemical co-precipitation followed by hydrolysis (CPH). Their visible light photocatalytic activity was investigated for the degradation of congo red (CR) dye. All NCs showed improved degradation as compared to the polycrystalline samples of similar compositions prepared by the solid-state reaction (SSR) route (average particle size of a few micrometers), as well as to the pure TiO(2). The better photocatalytic activity of the NCs was attributed to their smaller particle size. Another comparison of the results with those obtained with Zn(2+)/Fe(3+) ions co-doped TiO(2) NCs, under similar experimental conditions, revealed that in the Y(3+)-doped NCs, particle size might not be the only factor responsible for the improved photocatalytic properties. It was concluded that the Y(3+) ion-mediated suppression of the unwanted e(-)/h(+) recombination could be the possible factor leading to additional enhancement.