Electrochemical Characterisation of Platinum Nanoparticles Prepared in a Water-in-Oil Microemulsion in the Presence of Different Modifiers and Metal Precursors

In this work, water‐in‐oil microemulsions are used in the presence of various modifiers and metal precursors to obtain preferentially oriented Pt nanoparticles. Preferentially oriented cubic nanoparticles, enriched in (100) sites, are prepared using specific concentrations of HCl, HBr, H2SO4 and H3P...

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Published inChemElectroChem Vol. 3; no. 10; pp. 1601 - 1608
Main Authors Martínez-Rodríguez, Roberto A., Vidal-Iglesias, Francisco J., Solla- Gullón, José, Cabrera, Carlos R., Feliu, Juan M.
Format Journal Article
LanguageEnglish
Published Weinheim Blackwell Publishing Ltd 01.10.2016
John Wiley & Sons, Inc
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Summary:In this work, water‐in‐oil microemulsions are used in the presence of various modifiers and metal precursors to obtain preferentially oriented Pt nanoparticles. Preferentially oriented cubic nanoparticles, enriched in (100) sites, are prepared using specific concentrations of HCl, HBr, H2SO4 and H3PO4. By contrast, the use of citric and oxalic acids increases the amount of (111) sites, albeit not significantly. Nanoparticles are electrochemically characterised by hydrogen and Ge adsorption/desorption processes, as well as CO stripping. Finally, the electrocatalytic activity of the nanoparticles having the highest percentage of (100) sites is evaluated for ammonia oxidation, confirming the electrochemical characterisation results. The results obtained indicate that, 15 % HCl‐modified Pt nanoparticles synthesised using K2PtCl4 as metal precursor displayed the highest amount of (100) sites (46.7 %), and gave the highest peak current density for ammonia oxidation, around fivefold that of polyoriented Pt. Get in shape: Pt nanoparticles prepared in water‐in‐oil microemulsions in the presence of different surface modifiers are electrochemically characterized. Well‐defined cubic nanoparticles with a preferred (100) surface structure are obtained and tested in different electrocatalytic reactions.
Bibliography:ArticleID:CELC201600295
istex:B5C768C6E2E1E49E8307B9E3C57E7FFFC5650476
Generalitat Valenciana - No. PROMETEOII/2014/013
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SourceType-Scholarly Journals-1
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ISSN:2196-0216
2196-0216
DOI:10.1002/celc.201600295