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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Oezaslan, Mehtap
Technische Universität Braunschweig
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (16/16 displayed)
- 2024Monitoring the Morphological Changes of Skeleton-PtCo Electrocatalyst during PEMFC Start-Up/Shut-Downprobed by in situ WAXS and SAXScitations
- 2024Monitoring the Morphological Changes of Skeleton-PtCo Electrocatalyst during PEMFC Start-Up/Shut-Down probed by in situ WAXS and SAXS.citations
- 2024Tuning the morphology and chemical distribution of Ag atoms in Au rich nanoparticles using electrochemical dealloyingcitations
- 2023Chemical Insights into the Formation of Colloidal Iridium Nanoparticles from In Situ X-ray Total Scatteringcitations
- 2023Nanoporous Gold: From Structure Evolution to Functional Properties in Catalysis and Electrochemistry
- 2023Chemical Insights into the Formation of Colloidal Iridium Nanoparticles from In Situ X-ray Total Scattering:Influence of Precursors and Cations on the Reaction Pathwaycitations
- 2023Chemical Insights into the Formation of Colloidal Iridium Nanoparticles from In Situ X-ray Total Scattering:Influence of Precursors and Cations on the Reaction Pathwaycitations
- 2022Highly Durable Pt-Based Core-Shell Catalysts with Metallic and Oxidized Cobalt Species for Boosting the Oxygen Reduction Reaction
- 2022Nanoporous Copper Ribbons Prepared by Chemical Dealloying of a Melt-Spun ZnCu Alloycitations
- 2020Solvent-dependent growth and stabilization mechanisms of surfactant-free colloidal Pt nanoparticlescitations
- 2020Solvent-dependent growth and stabilization mechanisms of surfactant-free colloidal Pt nanoparticlescitations
- 2020The Dissolution Dilemma for Low Pt Loading Polymer Electrolyte Membrane Fuel Cell Catalystscitations
- 2018Structural Analysis and Electrochemical Properties of Bimetallic Palladium–Platinum Aerogels Prepared by a Two‐Step Gelation Processcitations
- 2018Solutions for catalysis: A surfactant-free synthesis of precious metal nanoparticle colloids in mono-alcohols for catalysts with enhanced performances
- 2017Durabilty of Pt-Based Alloy Nanoparticles Supported on Functionalized Carbon Materials for the ORR – Tuning the Interaction between Particles and Support Material
- 2015Noble Metal Aerogels - Synthesis, Characterization, and Application as Electrocatalysts
Places of action
Organizations | Location | People |
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article
Solvent-dependent growth and stabilization mechanisms of surfactant-free colloidal Pt nanoparticles
Abstract
<p>Understanding the formation of nanoparticles (NPs) is key to develop materials via sustainable routes. The Co4Cat TM process is a new synthesis of precious metal NPs in alkaline mono-alcohols well-suited to develop active nanocatalysts. The synthesis is 'facile', surfactant-free and performed under mild conditions like low temperature. Interestingly, this process is sensitive to parameters masked in other colloidal syntheses. The oxidation properties of the solvent are here shown to strongly influence the formation of Pt NPs. Based on the in situ formation of CO adsorbed on the NP surface by solvent oxidation, a model is proposed that accounts for the different growth and stabilization mechanisms as well as re-dispersion properties of the surfactant-free NPs in different solvents. Using in situ and ex situ characterizations, it is established that in methanol, a slow nucleation with a limited NP growth is achieved. In ethanol, a fast nucleation followed by continuous and pronounced particle sintering occurs. The results support further strategies to rationally design, investigate, control and produce improved NPs for fundamental and applied research.</p>