The CdSe and CdTe nanocrystals were successfully synthesized from the ultrasonic-assisted aerosol flow system using a surfactant/solvent system of oleic acid (OA)/trioctylphosphine (TOP)/trioctylphosphine oxide (TOPO)/octadecene (ODE). A comprehensive examination on the control of the CdSe and CdTe crystal structures and optical properties was performed as functions of reaction temperatures and amount of reaction media in the aerosol flow system. CdSe nanocrystals with spherical shape and having zinc blende structure were produced. It was found that the crystal structure and shape of CdSe are not affected by reaction temperature. However, it was found that reaction temperature significantly affects the crystal structure and morphology of CdTe. Zero-dimensional CdTe nanocrystals with spherical shape and having zinc blende structure were obtained at the temperature higher than 300 degrees C. Three-dimensional tetrapod-shaped CdTe nanocrystals having wurtzite structure were obtained at the temperature lower than 250 degrees C. Furthermore, the anisotropic growth was observed to be enhanced as increasing the amount of OA used at the temperature of 250 degrees C.
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http://dx.doi.org/10.1016/j.ultramic.2008.04.047 | DOI Listing |
Inorg Chem
January 2025
Department of Chemistry, University of Patras, Patras 265 04, Greece.
A new [DyBiOCl(saph)] () Werner-type cluster has been prepared, which is the first Dy/Bi polynuclear compound with no metal-metal bond and one of the very few Ln-Bi (Ln = lanthanide) heterometallic complexes reported to date. The molecular compound has been deliberately transformed to its 1-D analogue [DyBiO(N)(saph)] () via the replacement of the terminal Cl ions by end-to-end bridging N groups. The overall metallic skeleton of (and ) can be described as consisting of a diamagnetic {Bi} unit with an elongated trigonal bipyramidal topology, surrounded by a magnetic {Dy} equilateral triangle, which does not contain μ-oxo/hydroxo/alkoxo groups.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Cardiff University, School of Chemistry, Park Place, Main Building, CF10 3AT, Cardiff, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
Despite the remarkable advancements in hypervalent iodine chemistry, exploration of bromine and chlorine analogues remains in its infancy due to their difficult synthesis. Herein, we introduce six-membered cyclic λ3-bromanes and λ3-chloranes. Through single-crystal X-ray structural analyses and conformational studies, we delineate the crucial bonding patterns pivotal for the thermodynamic stability of these compounds.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Key Laboratory of Green Printing, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China.
Colloidal crystal engineering enables the precise construction of structures with remarkable properties. However, the flexible and synergistic regulation of multiple properties of colloidal crystals remains a significant challenge. Here, we inspire from Brazilian opals to self-assemble polymer nanoparticles in the gaps of a single-layer opal substrate to fabricate large-scale binary colloidal crystals (BCCs).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Nanjing Normal University, School of Chemistry and Materials Science, CHINA.
Metal hexacyanoferrates (HCFs), also known as Prussian blue analogues, are ideal cathodes for potassium-ion batteries (PIBs) due to their nontoxicity and cost-effectiveness. Nevertheless, obtaining metal HCF cathode materials with both long-term cycling stability and high rate performance remains a daunting challenge. In this study, we present mesoporous single-crystalline iron hexacyanoferrate (MSC-FeHCF) microspheres, featuring a single-crystalline structure that contains interconnected pores spanning the entire crystal lattice.
View Article and Find Full Text PDFChem Sci
December 2024
Instituto de Ciencia Molecular (ICMol), Universidad de Valencia c/Catedrático José Beltrán 2 Paterna 46980 Spain
We present the synthesis of a lanthanoid-organic framework (LOF) featuring a dynamic structure that exhibits tunable magnetic properties. The LOF undergoes breathing and gate-opening phenomena in response to changes in DMF content and N sorption, leading to the emergence of new crystal phases with distinct characteristics. Notably, the desolvated form of the LOF excels as a single-ion magnet, while the fully activated structure demonstrates impressive qubit properties, exhibiting Rabi oscillations up to 60 K.
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