Abstract

In this work, we demonstrate the power of a simple top-down electrochemical erosion approach to obtain Pt nanoparticle with controlled shapes and sizes (in the range from ~ 2 to ~ 10 nm). Carbon supported nanoparticles with narrow size distributions have been synthesized by applying an alternating voltage to macroscopic bulk platinum structures, such as disks or wires. Without using any surfactants, the size and shape of the particles can be changed by adjusting simple parameters such as the applied potential, frequency and electrolyte composition. For instance, application of a sinusoidal AC voltage with lower frequencies results in cubic nanoparticles; whereas higher frequencies lead to predominantly spherical nanoparticles. On the other hand, the amplitude of the sinusoidal signal was found to affect the particle size; the lower the amplitude of the applied AC signal, the smaller the resulting particle size. Pt/C catalysts prepared by this approach showed 0.76 A/mg mass activity towards the oxygen reduction reaction which is ~ 2 times higher than the state-of-the-art commercial Pt/C catalyst (0.42 A/mg) from Tanaka. In addition to this, we discussed the mechanistic insights about the nanoparticle formation pathways.

Highlights

  • The shape, size and composition of metallic nanoparticles (NPs) often play a decisive role in achieving specific surface functionality for various applications [1,2,3]

  • The wires are immersed into an electrolyte containing alkali metal cations, and the nanoparticles are eroded from the metal wires under these conditions

  • We systematically investigate the influence of the synthesis conditions on the geometry and structure of supported Pt nanoparticles

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Summary

Introduction

Nano Res. 2021, 14(8): 2762–2769 intercalated into the metal surface layer to produce intermetallic compounds. We demonstrate how to use simple synthesis parameters such as the applied electrode potential, frequency and electrolyte composition to produce carbon supported Pt nanoparticles of desired shape and size without any surfactants or reducing agents. In this top-down method the nanoparticles are eroded from the metal wire by applying an alternating voltage with a specific frequency. Extending the method to a three-electrode configuration enabled a precise control of the metal wire potential. Composition and voltage pulses we further support the hypothesis that the mechanism of NP formation by this approach is enabled by the presence of alkali metal cations. Pair distribution function (PDF) analysis reveals strained nature of particles, which indicates that particles are carved out of the bulk samples

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