Dealloying single phase alloys is known to generate a type of nanostructured porous metals with intriguing properties. In this study, nanoporous gold (NPG) made by dealloying Au-Ag is investigated as a novel electrode material for methanol electro-oxidation. Compared to bulk Au electrode, oxidation and subsequent reduction of NPG occur at significantly negative potentials in both acid and alkaline solutions. NPG shows great catalytic activity for methanol electro-oxidation, but the structure quickly coarsens upon long time potential cycling. Interestingly, after surface modification with only a tiny amount of platinum, NPG exhibits greatly enhanced electrocatalytic activity toward methanol oxidation in the alkaline solutions, which is exemplified by a broad and high anodic peak during the positive scan and two secondary oxidation peaks in the subsequent reverse scan. At the same time, SEM observation and long-time potential cycling both prove that Pt-NPG has much enhanced structure stability as compared with bare NPG.

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Exploring highly efficient and durable bifunctional electrocatalysts from earth-abundant low-cost transition metals is central to obtaining clean hydrogen energy through large-scale electrolytic water splitting. Porous nickel-cobalt nitride nanosheets on macroporous Ni foam (NF) are synthesized through facile electrodeposition followed by a one-step annealing process in a NH atmosphere. The transformation from a metal hydroxide into a metal nitride could efficiently enhance the electrocatalytic performance for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Interestingly, the incorporation of nickel further boosts the catalytic activity of cobalt nitride. When used as bifunctional electrocatalysts, the obtained nickel-cobalt nitride electrocatalyst shows good stability and superior catalytic performance toward both HER and OER with low overpotentials of 0.29 and 0.18 V, respectively, to achieve a current density of 10 mA cm . The good electrocatalytic performance was also evidenced by the fabrication of an electrolyzer for overall water splitting, which exhibits a high gas generation rate for hydrogen and oxygen with excellent stability during prolonged alkaline water electrolysis. The present work provides an efficient approach to prepare a 3 D interconnected porous nickel-cobalt nitride network with exposed inner active sites for overall water splitting.

Spherical silver and gold nanoparticles with narrow size distributions were conveniently synthesized in aqueous solution by a novel electrochemical method. The technological keys to the electrochemical synthesis of monodispersed metallic nanoparticles lie in the choice of an ideal stabilizer for the metallic nanoclusters and the use of a rotating platinum cathode. Poly(N-vinylpyrrolidone) (PVP) was chosen as the stabilizer for the silver and gold clusters. PVP not only protects metallic particles from agglomeration, but also promotes metal nucleation, which tends to produce small metal particles. Using a rotating platinum cathode effectively solves the technological difficulty of rapidly transferring the (electrochemically synthesized) metallic nanoparticles from the cathode vicinity to the bulk solution, avoiding the occurrence of flocculates in the vicinity of the cathode, and ensuring the monodispersity of the particles. The particle size and particle size distribution of the silver and gold nanoparticles were improved by adding sodium dodecyl benzene sulfonate (SDBS) to the electrolyte. The electrochemically synthesized nanoparticles were characterized by TEM and UV/Vis spectroscopy.

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A tiny amount of Pt was deposited in a quasi-two-dimensional form onto the nanoporous gold (NPG) substrate through a simple immersion-electrodeposition (IE) method, forming nanostructured bimetallic Pt-Au catalysts. Such Pt-Au nanostructures have much higher structural stability than the bare NPG; moreover, they exhibit better catalytic activity and stronger poison resistance than commercial Pt-Ru catalysts because of the synergistic effect of the bimetallic compositions.

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