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Nanospheres of Ag‐coated Fe3O4 were successfully synthesized and characterized. Photocatalytic properties of Fe3O4@Ag composites have been investigated using steady‐state studies and laser pulse excitations. Accumulation of the electrons in the Ag shell was detected from the shift in the surface plasmon band from 430 to 405 nm, which was discharged when an electron acceptor such as O2, Thionine (TH) or C60 was introduced into the system. Charge equilibration with redox couple such as C60●–/C60 indicated the ability of these core–shell structures to carry out photocatalytic reduction reactions. As well, outer Ag layer could boost charge separation in magnetic core through dual effects of Schottky junction and localized surface plasmonic resonance (LSPR)‐powered band gap breaking effect under sunlight irradiation; resulted in higher photocatalytic degradation of diphenylamine (DPA). The maximum photocatalytic degradation rate was achieved at optimum amount of Ag‐NP loading to products. Adsorption studies confirmed that degradation of DPA dominantly occurred in solution. Moderately renewability of the nanocatalysts under sunlight was due to oxidation and dissolution of the outer Ag layer.  相似文献   

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The engineering of novel catalytic nanomaterials that are highly active for crucial carbon–carbon bond formations, easily recoverable many times, and biocompatible is highly desirable in terms of sustainable and green chemistry. To this end, catalysts comprising dendritic “click” ligands that are immobilized on a magnetic nanoparticle (MNP) core, terminated by triethylene glycol (TEG) groups, and incorporate Pd nanoparticles (PdNPs) have been prepared. These nanomaterials are characterized by transmission electron microscopy (TEM), high‐resolution TEM, inductively coupled plasma analysis, Fourier transform infrared spectroscopy, X‐ray photoelectron spectra and energy‐dispersive X‐ray spectroscopy. They are shown to be highly active, dispersible, and magnetically recoverable many times in Suzuki, Sonogashira, and Heck reactions. In addition, a series of pharmacologically relevant or natural products were successfully synthesized using these magnetic PdNPs as catalyst. For comparison, related PdNP catalysts deposited on MNPs bearing linear “click” PEGylated ligands are also prepared. Strong positive dendritic effects concerning ligand loading, catalyst loading, catalytic activity, and recyclability are observed, that is, the dendritic catalysts are much more efficient than non‐dendritic analogues.  相似文献   

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The oxoplatinates Na2PtO2, Na2PtO3, ?K2PtO3”? and ?Rb2PtO3”?. Hitherto unknown Na2PtO2 (greyish black) was prepared. Na2PtO2 (orthorhombic, D—Immm; a = 4.585, b = 3.119, c = 9.588 Å) is isotypic with Li2CuO2. α-Na2PtO3 (darkyellow; red as single-crystals) is monoclinic, C—C2/c (a = 5.419, b = 9.385, c = 10.752 Å, β = 99.67°), Li2SnO3-type. According to 3-dimensional single crystal data hitherto unknown β-Na2PtO3 (red crystals) is an orthorhombic variant of the Li2SnO3-type (a = 18.838, b = 6.282, c = 9.062 Å, Z = 16, D—Fddd; parameters see text); R = 0.0809, R' = 0.0948 [256 reflexes (hk0—hk6)]. The Madelung part of the lattice energy (MAPLE) is calculated and discussed for α-, β-Na2PtO3, α- and β-PtO2. For the first time we got K2PtO3 and Rb2PtO3.  相似文献   

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The thermal decomposition of CoCO3 Co(OH)2 (H2O)0,5 in the temperature range from 20 to 600°C, in air as well as in a dynamic nitrogen atmosphere, employing TGA, DTA, chemical analysis, and X-ray analysis, has been investigated. The course of the process in N2 differs completely from that in air, passing through a number of stages. The most probable mechanism of decomposition is proposed and an interpretation of the phenomena is given.  相似文献   

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