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A fundamental step toward studying the unique properties of actinide nanomaterials is control over the shape of actinide nanoparticles. Toward this goal, this work demonstrates the effects of precursor identity and surfactant concentration on the shape of uranium dioxide (UO) nanoparticles. UO nanoparticles were synthesized by thermal decomposition of different precursors in the presence of oleylamine and oleic acid as surfactants. The size, shape, phase, and chemical composition of the nanoparticles was evaluated using transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), electron diffraction (ED), and U L-edge X-ray absorption fine-structure (XAFS) spectroscopy. Anisotropic UO nanocubes of ∼ 4 nm were obtained only with low surfactant concentrations, while increasing the surfactant concentration resulted in formation of nanoparticles with an isotropic, sphere morphology. The importance of precursor identity was also investigated by employing U(hfa), U(acac), UO(acac), and UO(hfa)·HO (where hfa = hexafluoracetylacetone and acac = acetylacetone) as precursors. The nanocube morphology was only observed when U(hfa) was used as a precursor. XAS allowed for comparison of the disorder in anisotropic vs isotropic UO nanoparticles.
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http://dx.doi.org/10.1021/acs.inorgchem.5c00189 | DOI Listing |
J Med Humanit
September 2025
Faculty of Humanities, Saxo Institute, Copenhagen Centre for Health Research in the Humanities, University of Copenhagen, Copenhagen, Denmark.
Communication and interaction with public authorities and healthcare professionals in Denmark primarily go through digital self-service platforms, requiring diverse skills and device access. In this article, we describe how senior citizens in Denmark handle and make sense of public digitalization through different forms of digital support. Through an ethnographic study of community-led initiatives of digital support, we highlight how senior citizens find socio-technical ways of managing digital obligations and argue that citizens' digital agency in day-to-day interactions with public digitalization relies heavily on distributed socio-material relations.
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
Department of Materials Chemistry, National Institute of Chemistry, Ljubljana 1000, Slovenia.
The electrochemical CO reduction (ECOR) on copper (Cu) remains one of the most promising pathways to convert CO into value-added products. However, it suffers from severe restructuring, resulting in the unknown structural identity of the ECOR active catalyst. Here, we show that dissolution-redeposition is the universal early-stage restructuring mechanism in ECOR, occurring across all the tested Cu morphologies, including foils, nanoparticles, oxide-derived films, and gas diffusion electrodes.
View Article and Find Full Text PDFMethods Enzymol
August 2025
Plant Biochemistry, Faculty of Biology and Biotechnology, Ruhr-University Bochum, Bochum, Germany. Electronic address:
The N-terminus of a protein has an important regulatory impact on its in vivo stability and half-life. Proteins destined to chloroplasts and mitochondria are synthesized as precursor proteins in the cytosol with an N-terminal peptide sequence that ensures their correct targeting. During their cytosolic passage, precursor proteins are exposed to the cytosolic protein degradation machinery, hence, their N-termini must comply with regulatory processes for proteolytic degradation in the cytosol.
View Article and Find Full Text PDFNucleic Acids Res
August 2025
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawinskiego 5a, 02-106 Warsaw, Poland.
An evolutionarily conserved ribosomal protein Rps29/uS14 participates in the assembly of late pre-40S particles. In yeast Saccharomyces cerevisiae, duplicate genes RPS29A and RPS29B encode two paralogous proteins with 91% sequence identity. Here, we report that loss of either paralog impairs final step of cytoplasmic processing of 20S pre-rRNA, which is a direct precursor of mature 18S ribosomal RNA (rRNA)-a component of small ribosomal subunit.
View Article and Find Full Text PDFCureus
July 2025
Pathology and Laboratory Medicine, University of California, Los Angeles, Los Angeles, USA.
Amyloidosis encompasses a group of disorders characterized by the accumulation of insoluble protein fibrils within the extracellular matrix. These fibrils originate from low molecular weight protein subunits, many of which circulate naturally in the bloodstream. The resulting deposits can occur in nearly any organ, with the clinical picture shaped by the type, distribution, and extent of amyloid involvement.
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