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Issue 24, 2016
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Tailoring ruthenium exposure to enhance the performance of fcc platinum@ruthenium core–shell electrocatalysts in the oxygen evolution reaction

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Abstract

The catalytic properties of noble metal nanocrystals are a function of their size, structure, and surface composition. In particular, achieving high activity without sacrificing stability is essential for designing commercially viable catalysts. A major challenge in designing state-of-the-art Ru-based catalysts for the oxygen evolution reaction (OER), which is a key step in water splitting, is the poor stability and surface tailorability of these catalysts. In this study, we designed rapidly synthesizable size-controlled, morphology-selective, and surface-tailored platinum–ruthenium core–shell (Pt@Ru) and alloy (PtRu) nanocatalysts in a scalable continuous-flow reactor. These core–shell nanoparticles with atomically precise shells were produced in a single synthetic step with carbon monoxide as the reducing agent. By varying the metal precursor concentration, a dendritic or layer-by-layer ruthenium shell can be grown. The synthesized Pt@Ru and PtRu nanoparticles exhibit noticeably higher electrocatalytic activity in the OER compared to that of pure Pt and Ru nanoparticles. Promisingly, Pt@Ru nanocrystals with a ∼2–3 atomic layer Ru cuboctahedral shell surpass conventional Ru nanoparticles in terms of both durability and activity.

Graphical abstract: Tailoring ruthenium exposure to enhance the performance of fcc platinum@ruthenium core–shell electrocatalysts in the oxygen evolution reaction

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Supplementary files

Article information


Submitted
29 Feb 2016
Accepted
13 May 2016
First published
17 May 2016

Phys. Chem. Chem. Phys., 2016,18, 16169-16178
Article type
Paper

Tailoring ruthenium exposure to enhance the performance of fcc platinum@ruthenium core–shell electrocatalysts in the oxygen evolution reaction

N. M. AlYami, A. P. LaGrow, K. S. Joya, J. Hwang, K. Katsiev, D. H. Anjum, Y. Losovyj, L. Sinatra, J. Y. Kim and O. M. Bakr, Phys. Chem. Chem. Phys., 2016, 18, 16169
DOI: 10.1039/C6CP01401A

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