Here we present the results of experimental study of magnetic properties of samarium clusters doped with a single oxygen atom. In a recent theoretical study it was observed that for pure Sm clusters a transition from fully non-magnetic to weakly magnetic occurs due to a valence change occurring at a size of eight atoms. Here we found, first, that pure Sm clusters could not be synthesized due to the strong oxidation tendency of Sm and the inability to sufficiently remove oxygen from the setup. Therefore, we studied Sm[Formula: see text]O clusters. Since the oxygen contributes to the binding, the valence transition for Sm[Formula: see text]O clusters may be expected to occur for a smaller cluster size than for pure Sm clusters. Indeed from our experiments the valence transition is indicated to occur for [Formula: see text] Sm atoms instead of [Formula: see text]. Furthermore, the observed magnetic moment as function of cluster size for Sm[Formula: see text]O clusters shows a strong dependency of the magnetic moment on the cluster size. A large total magnetic moment is observed for Sm[Formula: see text]O, Sm[Formula: see text]O, Sm[Formula: see text]O and Sm[Formula: see text]O compared to the smaller moment for Sm[Formula: see text]O to Sm[Formula: see text]O and Sm[Formula: see text]O to Sm[Formula: see text]O.
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http://dx.doi.org/10.1088/1361-648X/aaef20 | DOI Listing |
Cell Rep
November 2023
Stanford University School of Medicine, Department of Medicine, Divisions of Hematology, Stanford, CA 94305, USA. Electronic address:
Somatic copy number gains are pervasive across cancer types, yet their roles in oncogenesis are insufficiently evaluated. This inadequacy is partly due to copy gains spanning large chromosomal regions, obscuring causal loci. Here, we employed organoid modeling to evaluate candidate oncogenic loci identified via integrative computational analysis of extreme copy gains overlapping with extreme expression dysregulation in The Cancer Genome Atlas.
View Article and Find Full Text PDFNature
December 2020
Division of Hematology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.
The distal lung contains terminal bronchioles and alveoli that facilitate gas exchange and is affected by disorders including interstitial lung disease, cancer, and SARS-CoV-2-associated COVID-19 pneumonia. Investigations of these localized pathologies have been hindered by a lack of 3D in vitro human distal lung culture systems. Further, human distal lung stem cell identification has been impaired by quiescence, anatomic divergence from mouse and lack of lineage tracing and clonogenic culture.
View Article and Find Full Text PDFJ Phys Ther Sci
January 2017
Department of Physical Therapy, Hanlyo University, Republic of Korea.
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