| People | Locations | Statistics |
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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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Arenz, Matthias
University of Bern
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (23/23 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
- 2023The more the better:on the formation of single-phase high entropy alloy nanoparticles as catalysts for the oxygen reduction reactioncitations
- 2023Chemical Insights into the Formation of Colloidal Iridium Nanoparticles from In Situ X-ray Total Scatteringcitations
- 2023Tuning the chemical composition of binary alloy nanoparticles to prevent their dissolutioncitations
- 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
- 2023The more the better: on the formation of single-phase high entropy alloy nanoparticles as catalysts for the oxygen reduction reactioncitations
- 2023Formation of intermetallic PdIn nanoparticles: influence of surfactants on nanoparticle atomic structurecitations
- 2023The more the bettercitations
- 2022Nanocomposite Concept for Electrochemical In Situ Preparation of Pt–Au Alloy Nanoparticles for Formic Acid Oxidationcitations
- 2022Nanocomposite Concept for Electrochemical in Situ Preparation of Pt-Au Alloy Nanoparticles for Formic Acid Oxidationcitations
- 2022High entropy alloy nanoparticle formation at low temperatures
- 2021Operando SAXS study of a Pt/C fuel cell catalyst with an X-ray laboratory sourcecitations
- 2021The Gas Diffusion Electrode Setup as Straightforward Testing Device for Proton Exchange Membrane Water Electrolyzer Catalysts
- 2021Elucidating Pt-Based Nanocomposite Catalysts for the Oxygen Reduction Reaction in Rotating Disk Electrode and Gas Diffusion Electrode Measurementscitations
- 2021Bifunctional Pt-IrO2Catalysts for the Oxygen Evolution and Oxygen Reduction Reactionscitations
- 2021Bayesian optimization of high‐entropy alloy compositions for electrocatalytic oxygen reductioncitations
- 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
- 2018On the Preparation and Testing of Fuel Cell Catalysts Using the Thin Film Rotating Disk Electrode Methodcitations
- 2018Solutions for catalysis: A surfactant-free synthesis of precious metal nanoparticle colloids in mono-alcohols for catalysts with enhanced performances
Places of action
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article
Chemical Insights into the Formation of Colloidal Iridium Nanoparticles from In Situ X-ray Total Scattering
Abstract
Iridium nanoparticles are important catalysts for several chemical and energy conversion reactions. Studies of iridium nanoparticles have also been a key for the development of kinetic models of nanomaterial formation. However, compared to other metals such as gold or platinum, knowledge on the nature of prenucleation species and structural insights into the resultant nanoparticles are missing, especially for nanoparticles obtained from Ir<i><sub>x</sub></i>Cl<i><sub>y</sub></i> precursors investigated here. We use <i>in situ</i> X-ray total scattering (TS) experiments with pair distribution function (PDF) analysis to study a simple, surfactant-free synthesis of colloidal iridium nanoparticles. The reaction is performed in methanol at 50 °C with only a base and an iridium salt as precursor. From different precursor salts─IrCl<sub>3</sub>, IrCl<sub>4</sub>, H<sub>2</sub>IrCl<sub>6</sub>, or Na<sub>2</sub>IrCl<sub>6</sub>─colloidal nanoparticles as small as Ir<sub>∼55</sub> are obtained as the final product. The nanoparticles do not show the bulk iridium face-centered cubic (<i>fcc</i>) structure but show decahedral and icosahedral structures. The formation route is highly dependent on the precursor salt used. Using IrCl<sub>3</sub> or IrCl<sub>4</sub>, metallic iridium nanoparticles form rapidly from Ir<sub><i>x</i></sub>Cl<sub><i>y</i></sub><i><sup>n-</sup></i> complexes, whereas using H<sub>2</sub>IrCl<sub>6</sub> or Na<sub>2</sub>IrCl<sub>6</sub>, the iridium nanoparticle formation follows a sudden growth after an induction period and the brief appearance of a crystalline phase. With H<sub>2</sub>IrCl<sub>6</sub>, the formation of different Ir<sub><i>n</i></sub> (<i>n</i> = 55, 55, 85, and 116) nanoparticles depends on the nature of the cation in the base (LiOH, NaOH, KOH, or CsOH, respectively) and larger particles are obtained with larger cations. As the particles grow, the nanoparticle structure changes from partly icosahedral to decahedral. The results show that the synthesis of iridium nanoparticles from Ir<sub><i>x</i></sub>Cl<sub><i>y</i></sub> is a valuable iridium nanoparticle model system, which can provide new compositional and structural insights into iridium nanoparticle formation and growth.