| 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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Mamakhel, Aref
Aarhus University
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (21/21 displayed)
- 2024Synthesis and characterization of an organic-inorganic hybrid crystal
- 2022X-ray Electron Density Study of the Chemical Bonding Origin of Glass Formation in Metal–Organic Frameworkscitations
- 2022X-ray Electron Density Study of the Chemical Bonding Origin of Glass Formation in Metal–Organic Frameworkscitations
- 2022Composition space of PtIrPdRhRu high entropy alloy nanoparticles synthesized by solvothermal reactionscitations
- 2022Composition space of PtIrPdRhRu high entropy alloy nanoparticles synthesized by solvothermal reactionscitations
- 2022Combined characterization approaches to investigate magnetostructural effects in exchange-spring ferrite nanocomposite magnetscitations
- 2022Synthesis of Phase-Pure Thermochromic VO2 (M1)citations
- 2021Tailoring the stoichiometry of C 3 N 4 nanosheets under electron beam irradiationcitations
- 2021Tailoring the stoichiometry of C3N4 nanosheets under electron beam irradiation
- 2021Tailoring the stoichiometry of C3N4 nanosheets under electron beam irradiationcitations
- 2021Tuning of bandgaps and emission properties of light-emitting diode materials through homogeneous alloying in molecular crystalscitations
- 2019Promotion Mechanisms of Au Supported on TiO2 in Thermal- And Photocatalytic Glycerol Conversioncitations
- 2019General Solvothermal Synthesis Method for Complete Solubility Range Bimetallic and High-Entropy Alloy Nanocatalystscitations
- 2019Promotion Mechanisms of Au Supported on TiO 2 in Thermal- And Photocatalytic Glycerol Conversioncitations
- 2019In Situ In-House Powder X-ray Diffraction Study of Zero-Valent Copper Formation in Supercritical Methanolcitations
- 2019Promotion mechanisms of Au supported on TiO2 in thermal- and photocatalytic glycerol conversioncitations
- 2018Functionally Graded (PbTe)1-x(SnTe)x Thermoelectricscitations
- 2017In Situ PDF Study of the Nucleation and Growth of Intermetallic PtPb Nanocrystalscitations
- 2017Supercritical flow synthesis of Pt1-xRux nanoparticles: comparative phase diagram study of nanostructure versus bulkcitations
- 2016Electron Density Analysis of the "O-O" Charge-Shift Bonding in Rubrene Endoperoxidecitations
- 2015A Novel Dual-Stage Hydrothermal Flow Reactor
Places of action
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article
In Situ In-House Powder X-ray Diffraction Study of Zero-Valent Copper Formation in Supercritical Methanol
Abstract
Nano/micro crystalline copper is widely used in catalysts and it has potential for being used as conductive additive to ink for inkjet printed electronics. Copper is attractive, because it has excellent electrical conductivity and low cost compared to noble metals. The nucleation and phase transitions from the precursor to the final micrometer sized Cu in supercritical methanol have been studied for the first time using in-house in situ powder X-ray diffraction (PXRD). Temperatures have a significant impact on the reduction process of Cu2+, at low synthesis temperature (250 °C), it was observed how the Cu2+ precursor initially formed copper hydroxy nitrate (Cu2(OH)3NO3) and transformed to copper(II)oxide (CuO) i.e no reduction took place. At 300 °C multiple phase transformation could be observed from initial copper hydroxy nitrate to zero-valent copper, the in situ investigations reveal the following reaction scheme; CuII2(OH)3NO3 → CuIIO → CuI2O → Cu0. Increasing the synthesis temperature causes the pure Cu0 to form much faster; at 350 °C, it takes 8.7 min to produce phase pure Cu0, while at 450 °C, the formation takes ∼0.7 min. Increasing the initial concentration of Cu2+ in the precursor causes formation of larger Cu0 crystallites in the final product. Finally, the in situ observations were used as guidance for making Cu0 using a supercritical flow setup.