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  • World Scientific Pub Co Pte Ltd  (4)
  • 2010-2014  (4)
Type of Medium
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  • World Scientific Pub Co Pte Ltd  (4)
Language
Years
  • 2010-2014  (4)
Year
  • 1
    Online Resource
    Online Resource
    World Scientific Pub Co Pte Ltd ; 2012
    In:  Nano Vol. 07, No. 02 ( 2012-04), p. 1250013-
    In: Nano, World Scientific Pub Co Pte Ltd, Vol. 07, No. 02 ( 2012-04), p. 1250013-
    Abstract: ZnSnO 3 nanowires were synthesized on Si substrates by thermal evaporation of a mixture of ZnO, SnO 2 and graphite powders. The nanowires were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and photoluminescence spectroscopy. The ZnSnO 3 nanowires varied from 10 to 100 nm in diameter and up to a few hundred of micrometers in length. Transmission electron microscopy and X-ray diffraction revealed that the nanowires are multiphase nanostructures containing ZnSnO 3 , Zn 2 SnO 4 , ZnO, and SnO 2 phases. Photoluminescence measurements showed that ZnSnO 3 nanowires had a sharp ultraviolet emission peak at approximately 375 nm as well as a broad green emission band centered at approximately 510 nm. The violet emission of ZnSnO 3 nanowires exhibits a blue shift by approximately 5 nm compared to that of ZnO nanowires and the visible emission of ZnO nanowires shifted from the orange region to the green region, which should be attributed to the narrowing of E g . Thermal annealing enhanced the green emission but degraded the ultraviolet emission of the ZnSnO 3 nanowires. In addition, the origin of the enhanced luminescence of ZnSnO 3 nanowires compared to ZnO and SnO 2 nanowires is discussed.
    Type of Medium: Online Resource
    ISSN: 1793-2920 , 1793-7094
    Language: English
    Publisher: World Scientific Pub Co Pte Ltd
    Publication Date: 2012
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  • 2
    Online Resource
    Online Resource
    World Scientific Pub Co Pte Ltd ; 2011
    In:  Nano Vol. 06, No. 01 ( 2011-02), p. 93-99
    In: Nano, World Scientific Pub Co Pte Ltd, Vol. 06, No. 01 ( 2011-02), p. 93-99
    Abstract: We report the preparation and thermal annealing of SnO 2 -core/ TiO 2 -shell nanorods using a two-step process comprising the thermal evaporation of Sn powders and the sputter-deposition of TiO 2 . X-ray diffraction analysis revealed that the shells were crystallized by annealing. Photoluminescence measurements showed that the major yellow emission of the SnO 2 nanorods was enhanced in intensity by sheathing them with TiO 2 and was further enhanced by annealing. A reducing atmosphere was found to be more efficient in enhancing the yellow emission by annealing than an oxidative atmosphere. The origin of the emission enhancement by coating and annealing is also discussed.
    Type of Medium: Online Resource
    ISSN: 1793-2920 , 1793-7094
    Language: English
    Publisher: World Scientific Pub Co Pte Ltd
    Publication Date: 2011
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  • 3
    Online Resource
    Online Resource
    World Scientific Pub Co Pte Ltd ; 2010
    In:  Nano Vol. 05, No. 05 ( 2010-10), p. 287-293
    In: Nano, World Scientific Pub Co Pte Ltd, Vol. 05, No. 05 ( 2010-10), p. 287-293
    Abstract: ZnSe -core/ SnO 2 -shell nanorods have been prepared by using a two-step process comprising the thermal evaporation of ZnSe powders and the atomic layer deposition of SnO 2 . ZnSe nanorods have been grown by the thermal evaporation of ZnSe powders on gold-coated Al 2 O 3 (0001) substrates. The ZnSe -core/ SnO 2 -shell nanorods were 0.1–0.2 μm in diameter and up to a few tens of micrometers in length. Transmission electron microscopy and X-ray diffraction analysis results indicate that the cores and shells are single crystal zinc blende-type ZnSe and polycrystalline simple orthorhombic-type SnO 2 , respectively. Photoluminescence measurements show that the ZnSe -core/ SnO 2 -shell nanorods have a strong orange emission band centered at around 650 nm. The orange emission of the ZnSe nanorods is enhanced in intensity by coating them with SnO 2 and further enhanced by annealing them. A reducing atmosphere is more efficient in enhancing the orange emission than an oxidative atmosphere. The highest emission intensity is obtained for the shell layer thickness corresponding to 1500 ALD cycles. The orange emission enhancement by annealing is mainly attributed to the formation of Sn interstitials in the ZnSe cores during the annealing process.
    Type of Medium: Online Resource
    ISSN: 1793-2920 , 1793-7094
    Language: English
    Publisher: World Scientific Pub Co Pte Ltd
    Publication Date: 2010
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  • 4
    Online Resource
    Online Resource
    World Scientific Pub Co Pte Ltd ; 2011
    In:  Nano Vol. 06, No. 05 ( 2011-10), p. 455-460
    In: Nano, World Scientific Pub Co Pte Ltd, Vol. 06, No. 05 ( 2011-10), p. 455-460
    Abstract: TeO 2 nanorods functionalized with Pd were prepared by a three-step process comprising thermal evaporation of Te powders, Pd deposition by photo-reduction, and annealing. Sensors were fabricated by using the Pd -functionalized TeO 2 nanorods. Scanning electron microscopy images exhibited that the nanorods with diameters in a range of 50–100 nm and lengths of a few micrometers were covered with the Pd nanoparticles with an average diameter of ~ 15 nm. Transmission electron microscopy and X-ray diffraction analysis revealed that the nanorods were monocrystalline simple tetragonal TeO 2 . On the other hand, the nanoparticles on them were confirmed to be nanocrystalline face-centered cubic Pd . The multiple-networked TeO 2 nanorod sensors exhibited a sensitivity of 3.13% at 100 ppm NO 2 at 300°C, whereas the Pd -functionalized TeO 2 nanorod sensors exhibited a sensitivity of 11.97% under the same condition. The recovery time of TeO 2 nanorods was decreased considerably at every NO 2 concentration by the Pd -functionalization even if the response time decreased or increased slightly depending upon the NO 2 concentration. In addition, the origin of the enhancement of the sensing properties of the TeO 2 nanorods by functionalization with Pd is discussed.
    Type of Medium: Online Resource
    ISSN: 1793-2920 , 1793-7094
    Language: English
    Publisher: World Scientific Pub Co Pte Ltd
    Publication Date: 2011
    Library Location Call Number Volume/Issue/Year Availability
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