Intermetallic Pd-Sn Nanoparticles on Supports with High Metal Loading Facilitated by the Metal-Metal Bond for High-Performance Cooperative Catalysis.

Atomically monodispersed intermetallic catalysts comprising highly accessible active sites are ideal heterogeneous catalytic materials. Designing such types of nanocatalysts on carbonaceous supports with high loading, however, remains a formidable challenge. Demonstrated herein is an effective synthetic strategy to produce highly dispersed intermetallic Pd-Sn nanoparticles on various supports with high catalyst loading (upto 24 wt % Pd and 18 wt % Sn) using a discrete bimetallic Pd-Sn complex, which in turn is highly superior as compared to conventionally used methods using individual metal salts.

Nanoscale Ni-NiO-ZnO Heterojunctions for Switchable Dehydrogenation and Hydrogenation through Modulation of Active Sites.

Catalysts consisting of metal-metal hydroxide/oxide interfaces are highly in demand for advanced catalytic applications as their multicomponent active sites will enable different reactions to occur in close proximity through synergistic cooperation when a single component fails to promote it. To address this, herein we disclosed a simple, scalable, and affordable method for synthesizing catalysts consisting of nanoscale nickel-nickel oxide-zinc oxide (Ni-NiO-ZnO) heterojunctions by a combination of complexation and pyrolytic reduction. The modulation of active sites of catalysts was achieved by varying the reaction conditions of pyrolysis, controlling the growth, and inhibiting the interlayer interaction and Ostwald ripening through the efficient use of coordinated acetate and amide moieties of Zn-Ni materials (), produced by the reaction between hydrazine hydrate and Zn-Ni-acetate complexes.

Tetrametallic Copper Complex to Nanoscale Copper: Selective and Switchable Dehydrogenation-Hydrogenation under Light.

A discrete, photoactive, ultrafine copper nanocluster of fewer than hundreds of atoms with stimuli-responsive switchable redox-active states is highly desired to control two different antagonistic reactions. Herein, a mixed-valent tetrametallic copper complex (C-1) of N-O-N Schiff base ligand is disclosed, in which the five different Cu-Cu interactions were used to generate photoactive nanoscale copper [LCu , S-1] through the reduction of coordinated imine to the amine of C-1. The presence of a ligand provides stability and helps to homogenize the material (S-1) in the organic solvent.