Hao Liu, Hao Wang, Hanchi Ma, Bin Liu, Jianhui Yang
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引用次数: 0
Abstract
Integrated metallic nanomaterials composed of more than one type of metal expands the functionalities and nanocatalysts due to the multidimensional and synergistic effects. For a porous core-shell nanoparticles (NPs), there are abundant undercoordinated active sites and remarkable electron/mass transports, and the multimetallic synergy can improve the catalytic activity and durability. Here, a successive seed-mediated growth method was employed to synthesize Au core-porous Pd shell loaded Au NPs (denoted as Au@Pd-Au) superstructures. The introduction of Au particles on the surface of Au core-porous Pd shell NPs prevents oxidation of the porous Pd surfaces. Taking advantage of the porous superstructures and bimetallic synergy, the electrocatalytic ethanol oxidation performance, including activity and durability, of the Au@Pd-Au superstructures were significantly enhanced. We thus believe that the Au@Pd-Au superstructures with novel morphologies and functionalities can become an attractive electrocatalyst in direct ethanol fuel cells.
期刊介绍:
Materials Research Bulletin is an international journal reporting high-impact research on processing-structure-property relationships in functional materials and nanomaterials with interesting electronic, magnetic, optical, thermal, mechanical or catalytic properties. Papers purely on thermodynamics or theoretical calculations (e.g., density functional theory) do not fall within the scope of the journal unless they also demonstrate a clear link to physical properties. Topics covered include functional materials (e.g., dielectrics, pyroelectrics, piezoelectrics, ferroelectrics, relaxors, thermoelectrics, etc.); electrochemistry and solid-state ionics (e.g., photovoltaics, batteries, sensors, and fuel cells); nanomaterials, graphene, and nanocomposites; luminescence and photocatalysis; crystal-structure and defect-structure analysis; novel electronics; non-crystalline solids; flexible electronics; protein-material interactions; and polymeric ion-exchange membranes.