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The structural characterisation of actinide nanoparticles (NPs) is of primary importance and hard to achieve, especially for non-homogeneous samples with NPs less than 3 nm. By combining high-energy X-ray scattering (HEXS) and high-energy-resolution fluorescence-detected X-ray absorption near-edge structure (HERFD XANES) analysis, we have characterised for the first time both the short- and medium-range order of ThO NPs obtained by chemical precipitation. By using this methodology, a novel insight into the structures of NPs at different stages of their formation has been achieved. The pair distribution function revealed a high concentration of ThO small units similar to thorium hexamer clusters mixed with 1 nm ThO NPs in the initial steps of formation. Drying the precipitates at around 150 °C promoted the recrystallisation of the smallest units into more thermodynamically stable ThO NPs. HERFD XANES analysis at the thorium M edge, a direct probe for f states, showed variations that we have correlated with the breakdown of the local symmetry around the thorium atoms, which most likely concerns surface atoms. Together, HEXS and HERFD XANES are a powerful methodology for investigating actinide NPs and their formation mechanism.
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http://dx.doi.org/10.1002/chem.202003360 | DOI Listing |
J Synchrotron Radiat
September 2025
Department of Physics, University of Helsinki, PO Box 64, FI-00014 Helsinki, Finland.
Here, the uranium valence electronic structures in the perovskite-based ternary uranate systems NaUO, KUO and RbUO are reported on the basis of high-energy resolved fluorescence-detected X-ray absorption spectroscopy experiments at the U L edge and relativistic quantum chemistry calculations based on density functional theory. Advanced theoretical simulations allowed us to identify the origin of spectral features and to assess the impact of structural distortion within the oxygen octahedra. The octahedral crystal-field strength extracted from both experiments and calculations is reported for all three compounds.
View Article and Find Full Text PDFACS Nano
July 2025
Institute for Nanostructure and Solid-State Physics, Center for Hybrid Nanostructures, University of Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany.
Two-phase synthesis is a well-established approach for achieving precise control of the nanoparticle properties. However, studying and understanding chemical transformations in such a spatially heterogeneous system is challenging. In this work, we introduce a two-phase synthesis route for ZnS nanoparticles (ZnS NPs) at the water-toluene interface.
View Article and Find Full Text PDFEnviron Sci Technol
June 2025
Department of Civil & Environmental Engineering & Earth Sciences, University of Notre Dame, Notre Dame, Indiana 46556, United States.
To facilitate the continued use of commercial nuclear power and address environmental contamination, it is essential to understand the fate and transport of plutonium (Pu) in (sub)surface environments. Current geochemical models do not account for complexity in mineral assemblages, such as metal substitution or the role of nanoscale crystallite sizes. In this work, we studied mineralogically complex systems where Pu(V) was the sorbate and Al-substituted or nanoscale iron (oxyhydr)oxides were the sorbents.
View Article and Find Full Text PDFChem Asian J
May 2025
Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK.
We successfully synthesised ceria and Cu-doped ceria thin films on fluorine-doped tin oxide (FTO) glass using electrochemical deposition methods. Although X-ray diffraction characterisation did not confirm the presence of pure CeO phase, XPS and high-resolution fluorescence detection method to collect XANES data at Ce L3 edge confirmed the presence of only Ce and the spectral features resembled that of CeO in all the as-synthesised samples. In situ reactivity studies in the H atmosphere of these samples employing XANES data, recorded during the heating and cooling cycle, revealed the extent of Ce conversion to Ce.
View Article and Find Full Text PDFInorg Chem
May 2025
Institute of Resource Ecology, Helmholtz-Zentrum Dresden-Rossendorf, Bautzner Landstraße 400, 01328 Dresden, Germany.
The ZrO-CeO system is fundamental to various technological applications, yet unresolved questions persist regarding cation miscibility and the occurrence of metastable phases in the ZrCeO phase diagram. This work addresses these gaps through a comprehensive investigation of ZrCeO compositions with varying cerium concentrations and incorporating Eu as a luminescent probe. Synchrotron powder X-ray diffraction analysis unveiled a miscibility gap between 20 and 50 mol % cerium.
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