Vastly Synergistic Fe2CuNiS4-Nanoarchitectures Anchored 2D-Nano-Sandwich Derived from Flower-Like-CuFeS2/N-Graphene and Cube-Like-NiFeS2/N-CNTs for Water Oxidation and Nitrophenol Reduction

Abstract

Surface area, pore properties, synergistic behavior, homogenous dispersion, and interactions between carbon matrix and metal-nanostructures are the key factors for achieving the better performance of carbon-metal based (electro)catalysts. However, the traditional hydro- or solvothermal preparation of (electro)catalysts, particularly, bi- or tri-metallic nanostructures anchored graphene (G) or carbon nanotubes (CNTs), often pose to poor metal–support interaction, low synergism, and patchy dispersion. At first, bimetallic flower-like-CuFeS2/NG and cube-like-NiFeS2/NCNTs nanocomposites were prepared by solvothermal method. The resultant bimetallic nanocomposites were employed to derive the 2D-nano-sandwiched Fe2CuNiS4/NGCNTs-SW (electro)catalyst by a very simple and green urea-mediated “mix-heat” method. The desired physicochemical properties of Fe2CuNiS4/NGCNTs-SW such as multiple active sites, strong metal-support interaction, homogenous dispersion and enhanced surface area were confirmed by various microscopic and spectroscopic techniques. To the best of our knowledge, this is the first urea-mediated “mix-heat” method for preparing 2D-nano-sandwiched carbon-metal-based (electro)catalysts. The Fe2CuNiS4/NGCNTs-SW was found to be highly effective for alkaline-mediated oxygen evolution reaction at low onset potential of 284.24 mV, and the stable current density of 10 mA cm−2 in 1.0 m KOH for 10 h. Further, the Fe2CuNiS4/NGCNTs-SW demonstrated excellent catalytic activity in the reduction of 4-nitrophenol with good kapp value of 87.71 × 10−2 s−1 and excellent reusability over five cycles. Overall, the developed urea-mediated “mix-heat” method is highly efficient for the preparation of metal-nanoarchitectures anchored 2D-nano-sandwiched (electro)catalysts with high synergism, uniform dispersion and excellent metal-support interaction.