Cheng-Ke Xu

Hengyang Normal University, Heng-nan, Hunan, China

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Publications (2)0.58 Total impact

  • Gui-Ming Qiu · Cheng-Ke Xu · Chong Huang ·
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    ABSTRACT: A novel green emitting phosphor, Tb(3+)-doped Ca2SnO4, was prepared by the solid-state reaction. X-ray powder diffraction (XRD) analysis confirmed the formation of Ca2SnO4 : Tb3+. Photoluminescence measurements indicated that the phosphor exhibits bright green emission at about 543 nm under UV excitation. The excitation spectra of Ca(2-x)Tb(x)SnO4 appear to have a red shift with main peak from 254 to 260 nm. The emission spectra of Ca(2-x)Tb(x)SnO4 have four peaks ascribed to 5D4-7F(J) (where J = 6, 5, 4, 3) transitions of Tb3+ ions. Under the condition of low Tb3+ concentration, the 5D4-7F6 transition of Tb3+ showed a stark energy level split to three split peaks and the peak intensity of 481nm firstly increased with increasing Tb3+ concentration, then decreased. The dependence of luminescent intensity of Ca2 SnO4 : Tb3+ phosphor on the Tb3+ concentration was studied, and the results show that the luminescence intensity firstly increased with increasing Tb3+ concentration, then decreased, and reached the maximal value at 9 mol% Tb3+. According to the Dexter theory, the authors confirmed the concentration quenching mechanism of Tb3+ in Ca2 SnO4. The fluorescence lifetime of phosphor analysis shows that the average lifetime is 4.4 ms. The results indicated that Ca2 SnO4 : Tb3+ could be a potential candidate as a green-emitting powder phosphor.
    Guang pu xue yu guang pu fen xi = Guang pu 11/2011; 31(11):2906-9. DOI:10.3964/j.issn.1000-0593(2011)11-2906-04 · 0.29 Impact Factor
  • Gui-ming Qiu · Cheng-ke Xu · Chong Huang ·
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    ABSTRACT: The BaMoO4:Eu3+ phosphors were synthesized by solid-state method and were characterized by X-ray diffraction (XRD) and photoluminescence spectra. XRD analysis confirmed the formation of BaMoO4 at 800 degrees C and exhibited a tetragonal crystal structure. The excitation spectrum of samples showed one broad band and some peaks located behind 350 nm. The former was attributed to the charge transfer transition of Eu3+-O(2-), while the latter belonged to the f-f transitions of Eu3+ ions. The emission spectrum shows four peaks at 591, 615, 654 and 702 nm, respectively. The dominant peak is located at 615 nm due to the 5D0-7F2 electric dipole transition of Eu3+.
    Guang pu xue yu guang pu fen xi = Guang pu 05/2011; 31(5):1200-3. DOI:10.3964/j.issn.1000-0593(2011)05-1200-04 · 0.29 Impact Factor