Unique Cu@CuPt Core-Shell Concave Octahedron with Enhanced Methanol Oxidation Activity

ACS Appl Mater Interfaces. 2017 Oct 25;9(42):36817-36827. doi: 10.1021/acsami.7b11268. Epub 2017 Oct 11.

Abstract

Although tremendous efforts have been devoted to the exploration of cost-effective, active, and stable electrochemical catalysts, only few significant breakthroughs have been achieved up to now. Therefore, exploring new catalysts and improving catalyst activity and stability are still major tasks at present. Controllable synthesis of Pt-based alloy nanocrystals with a uniform high-index surface and unique architecture has been regarded as an effective strategy to optimize their catalytic efficiency toward electrochemical reactions. Accordingly, here we present a one-pot facile solvothermal process to synthesize novel unique Cu@CuPt core-shell concave octahedron nanocrystals that exhibit both outstanding activity and long durability. By regulating temperatures during the synthesis process, we were able to control the reduction rate of Cu and Pt ions, which could subsequently lead to the sequential stacking of Cu and Pt atoms. Owing to the concave structure, the as-prepared core-shell nanoparticles hold a high-index surface of {312} and {413}. Such surfaces can provide a high density of atomic steps and terraces, which is suggested to be favorable for electrochemical catalysts. Specifically, the Cu@CuPt core-shell concave octahedron presents 8.6/13.1 times enhanced specific/mass activities toward the methanol oxidation reaction in comparison to those of a commercial Pt/C catalyst, respectively. Meanwhile, the as-prepared catalyst exhibits superior durability and antiaggregation properties under harsh electrochemical conditions. The facile method used here proposes a novel idea to the fabrication of nanocrystals with desired compositional distribution, and the as-prepared product offers exciting opportunities to be applied in direct methanol fuel cells.

Keywords: CuPt; concave octahedron; core−shell; high-index; methanol oxidation reaction.