Abstract

Platinum is ubiquitous in electrochemical catalysis owing to its ability to accelerate redox reactions involving surface-bound hydrogen and oxygen. Accordingly, Pt is used as a calibration standard and activity benchmark against which novel electrocatalysts are compared. These measurements are often executed in unpurified, reagent grade electrolytes where Pt is also susceptible to deactivation by several routes. This constitutes a challenge where the ease of making measurements with Pt-based catalysts must be balanced against the difficulty of obtaining accurate and consistent results. We report herein a synthetic procedure for unsupported Pt nanoparticles that uses readily available reagents and laboratory apparatus, with the goal of making high-quality control experiments in electrocatalysis as accessible as possible. We also identified conditions under which these particles deactivate in unpurified aqueous acid and base and differentiated between mechanisms involving catalyst poisoning, which dominates at more negative applied potentials, and particle growth, which dominates at positive potentials where Pt-oxide species are produced. Finally, we demonstrated that unsupported Pt nanoparticle films can be used to good effect for reference electrode calibration and benchmarking of hydrogen evolution/oxidation electrocatalysts, even in unpurified electrolytes, provided steps are taken to minimize the impact of deactivation.

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