Cadmium oxide (CdO) is a yellowish to reddish-brown inorganic compound known for its semiconductor properties. With a density of 8.15 g/mL at 25 °C, CdO serves as a versatile reagent and catalyst in various chemical reactions. It is primarily used in the production of cadmium-based materials and as a catalyst in organic synthesis. Cadmium oxide is also utilized in the manufacturing of glass and ceramics, where it contributes to color and opacity. Our high-purity cadmium oxide powder, with a purity of 99.5% trace metals basis, is particularly valuable for applications that require minimal impurities.
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We used low-temperature reactions to synthesize different-sized CdSe quantum dots (QDs) capped with fatty-acid and phosphine ligands. From the correlation of high-resolution transmission electron microscopy and X-ray diffraction (XRD) analyses of the synthesized QDs, we observed size-dependent shape anisotropy. In
Small (Weinheim an der Bergstrasse, Germany), 7(7), 957-964 (2011-03-10)
The simple, template-free, low-temperature, large-scale synthesis of nanostructured CdS with the hexagonal wurtzite phase from bulk cadmium oxide under solid-phase conditions is demonstrated for the first time. The novel approach involves the homogenization of cadmium oxide (CdO) and thiourea in
Dalton transactions (Cambridge, England : 2003), (11)(11), 1431-1436 (2008-03-07)
A novel heterometallic 1D coordination polymer [{Ni(en)2}2(micro-NCS)4Cd(NCS)2](n) x nCH3CN (en = ethylenediamine) has been prepared using the self-assembly process in a one-pot reaction of cadmium oxide, nickel and ammonium thiocyanates with an acetonitrile solution of ethylenediamine. The complex consists of
CdZnO/ZnO quantum well (QW) samples are grown on GaN and ZnO templates with plasma-assisted molecular beam epitaxy under different conditions of substrate temperature, Cd effusion cell temperature, and O(2) flow rate for emission characteristics comparison. It is found that the
Nanoparticles of a three-dimensional supramolecular Cd(II) compound, [Cd(L)(2)(H(2)O)(2)] (1), (L(-)=1H-1,2,4-triazole-3-carboxylate), have been synthesized by a sonochemical process and characterized by scanning electron microscopy, X-ray powder diffraction, IR spectroscopy and elemental analyses. The thermal stability of compound 1 in both its
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