Abstract

Lattice distortions and defects can lead to a strain effect that greatly affects the electronic structure of the noble metal surface and the chemical adsorption of ligands on the surfaces. Introducing defects is an efficient strategy to improve the activity of noble metal catalysts. Herein, a fusion approach is developed to fine-tune the defects and lattice strain in Au-Pd nanowires. Specifically, braided strands in Au-Pd nanoropes gradually coalesce to form solid nanowires upon H2 O2 treatment and heating, leading to a series of Au-Pd nanowires with various amounts of defects. Owing to the 1D morphology, as well as the optimized lattice strain and surface electronic structure, the intermediate Au-Pd nanowire obtained after 60min heating (denoted as Au-Pd NW60 ) exhibits excellent catalytic activity and stability toward the oxygen reduction reaction, with the half-wave potential at 0.918V, 45mV higher than that of the commercial Pt/C; and specific activity reaches up to 1.7mA cm-2 , 7.3 times higher than that of the Pt/C.

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