nanoparticles were prepared by sol-gel method and were dispersed in the sol to obtain luminescent thin films through dip-coating process. XRD
SEM
TEM
FTIR
UVPC and PL were used to characterized the nanoparticles and transparent films. The results indicated that the oleic-acid was removed from the nanoparticles and SiO
2
was coated on the particles successfully. The SiO
2
shell has no influence on the crystalline structure and its fluorescence perfor-mance declines slightly. The morphology of -NaYF
4
: Eu
3+
transforms to nanospheres due to the solvent solution and tension of network structure of SiO
2
. The nanoparticles were dispersed in the thin films uniformly
and the films also have good transmittance and minus reflection effect. After coating and thermal treatment
the luminescence intensity from 420 to 500 nm was enhanced owing to the oxygen vacancy. But the luminescence at 613 nm quenches because of the energy transfer and nonradiative transition. The optimal technological parameters of the films were obtained by testing.
关键词
Keywords
references
Weissleder R, Ntziachristos V. Shedding light onto live molecular targets [J]. Nat. Med., 2003, 9(1):123-128.[2] Intes X, Ripoll J, Chen Y, et al. In vivo continuous-wave optical breast imaging enhanced with Indocyanine [J]. Green Med. Phys., 2003, 30(6):1039-1047.[3] Imbert D, Cabtuel M, Bunzli J C, et al. Extending lifetimes of lanthanide-based near-infrared emitters (Nd, Yb) in the millisecond range through Cr(III) sensitization in discrete bimetallic edifices [J]. J. Am. Chem. Soc., 2003, 125(51):15698-15699.[4] Wolcott A, Gerion D, Visconte M, et al. Silica-coated CdTe quantum dots functionalized with thiols for bioconjugation to IgG proteins [J]. J. Phys. Chem. B, 2006, 110(11):5779-5789.[5] Feng L Y, Kong X G. Preparation and characterization of fluorescence CdSe-liposome compound [J]. Chin. J. Lumin.(发光学报), 2007, 28(3):417-420 (in Chinese).[6] Feng B, Teng F, Tang A W, et al. Application of aminophenol-stabilized CdSe nanocrystals as a fluorescent label for lysozyme [J]. Chin. J. Lumin.(发光学报), 2007, 28(3):421-424 (in Chinese).[7] Qian H F, Dong C Q, Peng J L, et al. High-quality and water-soluble near-infrared photoluminescent CdHgTe/CdS quantum dots prepared by adjusting size and composition [J]. J. Phys. Chem. C, 2007, 111(45):16852-16857.[8] Bailey R E, Nie S M. Alloyed semiconductor quantum dots: Tuning the optical properties without changing the particle size [J]. J. Am. Chem. Soc., 2003, 125(23):7100-7106.[9] Derfus A M, Chan W C W. Probing the cytotoxicity of semiconductor quantum dots [J]. Nano Lett., 2004, 4(l):11-18.[10] Buse G, Preda E, Stef M, et al. Influence of Yb3+ ions on the optical properties of double-doped Er,Yb:CaF2 crystals [J]. Physica Scripta, 2011, 83(2):025604.[11] Sharma Y K, Surana S S L, Singh R K. Spectral studies of erbium doped soda lime silicate glasse in visible and near infrared regions [J]. Opt. Mater., 2007, 29(6):598-604.[12] Mizoguchi H, Woodward P W, Park C, et al. Strong near-infrared luminescence in BaSnO3 [J]. J. Am. Chem. Soc., 2004, 126(31):9796-9800.[13] Sano H, Herber R H. On the mssbauer parameters of bariumstannate [J]. Inorg. Nucl. Chem., 1968, 30(2):409-413.[14] Wagner G, Binder H. Untersuchung der binaren systeme BaO-SnO2 und BaO-PbO2.I. phasenanalysen [J]. Z. Anorg. Allg. Chem., 1958, 297:328-346.[15] Udawatte C P, Yoshimura M. Preparation of well-crystallized BaSnO3 powders under hydrothermal conditions [J]. Mater. Lett., 2001, 47(1/2):7-10.[16] Lu W S, Schmidt H. Hydrothermal synthesis of nanocrystalline BaSnO3 using a SnO2·xH2O sol [J]. J. Eur. Ceram. Soc., 2005, 25(6):919-925.[17] Lu W S, Schmidt H. Synthesis of tin oxide hydrate (SnO2·xH2O) gel and its effects on the hydrothermal preparation of BaSnO3 powders [J]. Adv. Powder Technol., 2008, 19(1):1-12.[18] Lu W S, Schmidt H. Lyothermal synthesis of nanocrystalline BaSnO3 powders [J]. Ceram. Inter., 2008, 34(3):645-649.[19] de Boer W D A M, Timmerman D, Dohnalova K, et al. Red spectral shift and enhanced quantum efficiency in phonon-free photoluminescence from silicon nanocrystals [J]. Nat. Nanotechnol., 2010, 5(12):878-884.