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檸檬酸螯合法制備BaHfO3:Ce3+納米材料及其發(fā)光特性
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遼寧省自然科學(xué)基金(20062001)和遼寧省科技攻關(guān)計(jì)劃(2005222009)


Preparation and Luminescence Characteristics of Nano BaHfO3:Ce3+ Powders Prepared by Citric Acid Chelating Process
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    摘要:

    通過檸檬酸螯合法合成BaHfO3:Ce3+納米粉體。采用TG-DTA、XRD、SEM等手段對粉體進(jìn)行了表征,用熒光光度儀分析樣品的激發(fā)光譜和發(fā)射光譜。結(jié)果表明:在CA:EG=1:3的條件下得到干凝膠前驅(qū)體,經(jīng)1050 ℃煅燒2 h,合成出結(jié)晶度高、近似球形、粒徑尺寸約為40 nm的BaHfO3:Ce3+納米粉體。Ce3+摻雜濃度為0.9 mol%的BaHfO3:Ce3+樣品激發(fā)光譜和發(fā)射光譜的相對強(qiáng)度最大。激發(fā)光譜有兩個較寬的譜帶,發(fā)光峰值分別在393和445 nm波長處最大。樣品在393和445 nm的

    Abstract:

    Citric acid chelating method was used to prepare Ce3+ doped BaHfO3 nano-powder. TG-DTA, XRD and SEM were employed to characterize the powder. The excitation and emission spectra of the specimens were analyzed by the fluorescence photometer. Results show that BaHfO3:Ce3+ nanometer powder with high degree of crystallinity, nearly spherical morphology and 40 nm particle size could be synthesized after the precursor gel prepared under the condition of CA:EG=1:3 was calcined at 1050 ℃ for 2 h. The maximum relative intensities of the excitation spectra and emission spectra appeared for the BaHfO3:Ce3+ specimen with Ce3+ doped concentration of 0.9 mol%. The excitation spectrum has two relatively wide spectrum bands where there are maximum peak values at the wavelength of 393 nm and 445 nm, respectively. The emission spectra at lex= 393 nm and lex=445 nm also have two spectrum bands where exist maximum peak values at 530 nm and 590 nm, respectively, corresponding to 5d→2F5/2 and 5d→2F7/2 transitions of Ce3+ cation, respectively. The emission spectra at 393 nm and 445 nm are obviously different, because the 4f ground State of Ce3+ cation is formed by two energy levels, with the energy difference of about 2000 cm-1.

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王華棟,馬偉民,聞 雷,尹 凱,沈世妃.檸檬酸螯合法制備BaHfO3:Ce3+納米材料及其發(fā)光特性[J].稀有金屬材料與工程,2009,38(8):1446~1449.[Wang Huadong, Ma Weimin, Wen Lei, Yin Kai, Shen Shifei. Preparation and Luminescence Characteristics of Nano BaHfO3:Ce3+ Powders Prepared by Citric Acid Chelating Process[J]. Rare Metal Materials and Engineering,2009,38(8):1446~1449.]
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  • 收稿日期:2008-10-18
  • 最后修改日期:2009-03-15
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