Effects of Ag doping on the crystallinity and optical properties of zinc oxide (ZnO) nanoparticles have been studied by x-ray diffraction, diffuse reflectance spectroscopy, micro-Raman, and photoluminescence spectroscopy. It has been observed that while Ag-doping at low concentration improves the optoelectronic properties of ZnO nanostructures, Ag-doping at high concentrations drastically modify the emission behavior and lattice vibrational characteristics of the nanostructures. High Ag content in ZnO nanostructures causes lattice deformation, induces silent vibrational modes in Raman spectra, and reduces excitonic UV emission due to concentration quenching.
An improved synthetic method has been designed and demonstrated to reproducibly generate hollow gold nanospheres (HGNs) with strong surface plasmon resonance (SPR) absorption in the near infrared (NIR). The HGNs have been synthesized via galvanic replacement of cobalt with gold while utilizing different amounts of poly(vinylpyrrolidone) (PVP) as a template stabilizing agent. Ninety percent of syntheses performed by this modified method resulted in HGNs with an SPR near 800 nm, which is highly desirable for biomedical applications such as photothermal ablation (PTA) therapy, while other polymers (PAA and PEG) did not. Based on absorption and TEM measurements, PVP stabilizes the cobalt template particles via carbonyl-induced stabilization that slows nucleation and growth of the gold shell allowing for the generation of a reproducibly thin shell, thereby inducing a significant red shift of the SPR to 800 nm. The results are significant to various potential applications of HGNs, e.g. cancer therapy and sensing.
Facile and reproducible SERS signals from Shewanella oneidensis were obtained utilizing silver nanoparticles (AgNPs) and silver nanowires (AgNWs). Additionally, SERS images identify the distribution of SERS hot-spots. One important observation is the synergistically enhanced SERS signal when AgNPs and AgNWs are used in conjunction, due to constructively enhanced electromagnetic field.
Emission, excitation, and polarization spectra as well as decay kinetics are studied at 4.2 to 500 K for the luminescence of BC' + centres in two crystals (KC1 and CaO) with strongly different electron-phonon interaction. It is concluded that three bands at -2.5, 3.11, and -1.5 eV, observed in the emission spectrum of the KC1 : Bi, S crystal belong to the same centre, but arise from states of different origin. The splitting of the 2.5 eV band, caused by the presence of a defect (S2-) near a Bi'+ ion is detected. Besides the well-known triplet 3.3 and 3.1 eV bands, a new 4.15 eV emission is found in CaO :Bi crystal, which is ascribed to transitions from the singlet excited state of the Bi3+ ion. The structure and the parameters of the relaxed excited states are determined and the models of the corresponding BiJt centres are discussed.
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