浏览全部资源
扫码关注微信
湖南师范大学化学化工学院 资源精细化与先进材料湖南省高校重点实验室,湖南 长沙,410081
纸质出版日期:2018-5-5,
网络出版日期:2017-11-23,
收稿日期:2017-8-18,
修回日期:2017-10-24,
扫 描 看 全 文
李金银, 彭志雄, 余丽萍等. Si,Lu掺杂Ca<sub>0.8</sub>Zn<sub>0.2</sub>TiO<sub>3</sub>:Pr<sup>3+</sup>荧光粉的光学性能改善[J]. 发光学报, 2018,39(5): 643-652
LI Jin-yin, PENG Zhi-xiong, YU Li-ping etc. Improved Luminescence Properties of Ca<sub>0.8</sub>Zn<sub>0.2</sub>TiO<sub>3</sub>:Pr<sup>3+</sup> Phosphors Doped with Si and Lu[J]. Chinese Journal of Luminescence, 2018,39(5): 643-652
李金银, 彭志雄, 余丽萍等. Si,Lu掺杂Ca<sub>0.8</sub>Zn<sub>0.2</sub>TiO<sub>3</sub>:Pr<sup>3+</sup>荧光粉的光学性能改善[J]. 发光学报, 2018,39(5): 643-652 DOI: 10.3788/fgxb20183905.0643.
LI Jin-yin, PENG Zhi-xiong, YU Li-ping etc. Improved Luminescence Properties of Ca<sub>0.8</sub>Zn<sub>0.2</sub>TiO<sub>3</sub>:Pr<sup>3+</sup> Phosphors Doped with Si and Lu[J]. Chinese Journal of Luminescence, 2018,39(5): 643-652 DOI: 10.3788/fgxb20183905.0643.
采用高温固相法合成Ca
0.8
Zn
0.2
TiO
3
:0.2% Pr
3+
,Si
4+
和Ca
0.8
Zn
0.2
TiO
3
:0.2% Pr
3+
,Si
4+
,Lu
3+
荧光粉。通过X射线衍射仪、电子顺磁共振光谱仪、显微拉曼光谱仪和荧光光谱仪等表征了该系列荧光粉的物相组成、微观结构和发光性质。结果表明,以-Si
3
N
4
为硅源制备的荧光粉具有最佳的光学性能。加入ZnO后,荧光粉由CaTiO
3
、Zn
2
TiO
4
和Ca
2
Zn
4
Ti
16
O
38
三相组成,其中CaTiO
3
为主相。电子顺磁共振谱证实了Pr
4+
存在,Lu
3+
的添加使[Pr
4+
Ti
3+
O
3
]
+
簇显著增加,电子顺磁共振谱和拉曼光谱均证实Si
4+
、Lu
3+
的掺杂使局部TiO
6
簇对称性提高,有利于Pr
3+
发光中心的能量传递。在336 nm激发下,荧光粉展示了很强的位于612 nm的红光发射(归属于Pr
3+
的
1
D
2
3
H
4
跃迁)及理想的红光色坐标(x=0.670,y=0.330)。Si
4+
和Lu
3+
的添加显著增强了370 nm激发下红光发射,Ca
0.8
Zn
0.2
TiO
3
:0.2% Pr
3+
,3.2% Si
4+
荧光粉的余辉寿命最长。
Ca
0.8
Zn
0.2
TiO
3
:0.2%Pr
3+
Si
4+
and Ca
0.8
Zn
0.2
TiO
3
:0.2%Pr
3+
Si
4+
Lu
3+
phosphors were synthesized by high temperature solid-state method. Crystalline phase
microstructure and luminescence properties of phosphors were characterized with X-ray diffractometer (XRD)
electron paramagnetic resonance spectrometer (EPR)
microscopic Raman spectrometer and photoluminescence spectrometer
respectively. The results show that phosphor prepared using -Si
3
N
4
as Si source has the optimal luminescence properties. Phosphors with the addition of ZnO were confirmed to be constituted of CaTiO
3
Zn
2
TiO
4
and Ca
2
Zn
4
Ti
16
O
38
and CaTiO
3
is major phase. EPR spectra confirm that the presence of Pr
4+
and[Pr
4+
Ti
3+
O
3
]
+
clusters remarkably increase with the Lu
3+
addition. Increasing local symmetry of TiO
6
clusters with the addition of Si
4+
and Lu
3+
is verified by EPR and Raman spectra
which is beneficial for the energy transfer of luminescent center Pr
3+
. The obtained phosphor exhibited the intense red emission centered at 612 nm (originated from
1
D
2
3
H
4
transition of Pr
3+
) with an ideal chromaticity coordinate located at (x=0.670
y=0.330) under 336 nm excitation. Red emission excited by 370 nm remarkably increases with the addition of Si
4+
and Lu
3+
. The synthetic Ca
0.8
Zn
0.2
TiO
3
:0.2%Pr
3+
3.2%Si
4+
phosphor has the longest average lifetime.
Ca0.8Zn0.2TiO3:Pr3+&beta-Si3N4Lu3+掺杂红色长余辉
Ca0.8Zn0.2TiO3:Pr3+&beta-Si3N4Lu3+ dopedred long persistence
YAMAMOTO H, MATSUZAWA T. Mechanism of long phosphorescence of SrAl2O4:Eu2+, Dy3+ and CaAl2O4:Eu2+, Nd3+[J]. J. Lumin., 1997, 72:287-289.
ZHANG C, DENG C Y. Improved preparation technology of color-tunable long afterglow phosphors Sr1.94-xCaxMgSi2O7:Eu0.012+, Dy0.053+[J]. J. Lumin., 2017, 192:310-315.
崔彩娥, 雷星, 黄平, 等. EDTA络合溶胶-凝胶法制备Y2O2S:Eu3+,Mg2+,Ti4+红色长余辉材料[J]. 发光学报, 2013, 34(4):416-420. CUI C E, LEI X, HUANG P, et al.. Synthesis of red long lasting phosphors Y2O2S:Eu3+, Mg2+, Ti4+ by EDTA complexing sol-gel method[J]. Chin. J. Lumin., 2013, 34(4):416-420. (in Chinese)
王磊, 董杰, 黄平, 等. 碱土金属离子对红色长余辉材料Y2O2S:Eu3+, M2+(M=Mg,Ca,Sr,Ba),Ti4+纳米阵列发光性能的影响[J]. 发光学报, 2014, 35(5):553-557. WANG L, DONG J, HUANG P, et al.. Influence of alkaline-earth metal ions on the luminescence properties of Y2O2S:Eu3+, M2+ (M=Mg, Ca, Sr, Ba), Ti4+ nanotube arrays[J]. Chin. J. Lumin., 2014, 35(5):553-557. (in Chinese)
KOJIMA Y, TAKAHASHI A, UMEGAKI T. Synthesis of orange-red-emitting Eu2+, Pr3+codoped SrS long afterglow phosphor[J]. J. Lumin., 2014, 146(1):42-45.
DIALLO P T, BOUTINAUD P, MAHIOU R, et al.. Red luminescence Pr3+ -doped calcium titanates[J]. Phys. Stat. Sol.(a), 1997, 160:255-263.
VIDYADHARAN V, MOHAN R, JOSEPH C, et al.. Luminescent characteristic of UV excited Sr0.5Ca0.5TiO3:Pr3+ reddish-orange phosphor[J]. Mater. Chem. Phys., 2016, 170(1):38-43.
SUN H Q, ZHANG Q W, WANG X H, et al.. Strong red emission in Pr3+-doped (K0.5Na0.5)NbO3-CaTiO3 diphase ceramics[J]. J. Am. Ceram. Soc., 2014, 98(2):601-606.
TANG J, YU X, YANG L, et al.. Preparation and Al3+ enhanced photoluminescence properties of CaTiO3:Pr3+[J]. Mater. Lett., 2006, 60(3):326-329.
NOTO L L, PITALE S S, GUSOWKI M A, et al.. Afterglow enhancement with In3+ codoping in CaTiO3:Pr3+ red phosphor[J]. Powder Tech., 2013, 237:141-146.
MAR B, SINGH K C, CEMBRERO-COCA P, et al.. Red emitting MTiO3(M=Ca or Sr) phosphors doped with Eu3+ or Pr3+ with some cations as co-dopants[J]. Displays, 2013, 34:346-351.
ZHANG X, ZHANG J, ZHANG X, et al.. Enhancement of the red emission in CaTiO3:Pr3+ by addition of rare earth oxides[J]. Chem. Phys. Lett., 2007, 434:237-240.
ZHANG J C, WANG X, YAO X. Enhancement of luminescence and afterglow in CaTiO3:Pr3+ by Zr substitution for Ti[J]. J. Alloys Compd., 2010, 498(2):152-156.
HOLLIDAY K S, KOHLGRUBER T A, TRAN I C, et al.. Increased fluroescence intensity in CaTiO3:Pr3+ phosphor due to NH3 treatment and Nb co-doping[J].Opt. Mater., 2016, 60:359-365.
YANG P, TAI B, WU W, et al.. Tailoring lanthanide doping in perovskite CaTiO3 for luminescence applications[J]. Phys. Chem. Chem. Phys., 2017, 19(24):16189-16197.
ROYCE M R, MATSUDA S, TAMAKI H, et al.. Red emitting long decay phosphors:US, 5650094[P]. 1997-07-22.
LIAN S X, ZUO C G, YIN D L, et al.. Preparation and characterization of red luminescent Ca0.8Zn0.2TiO3:Pr3+, Na+ nanophosphor[J]. J. Chin. Rare Earth Soc., 2006, 24(2):158-162.
YU L P, XIA M, CHEN X, et al.. Improvement of luminescence properties of Ca0.8Zn0.2TiO3:Pr3+ prepared by hydrothermal method[J]. J. Mater. Res., 2013, 28(18):2590-2597.
ZHANG X, ZHANG J, REN X, et al.. The dependence of persistent phosphorescence on annealing temperatures in CaTiO3:Pr3+ nanoparticles prepared by a coprecipitation technique[J]. J. Sol. State Chem., 2008, 181(3):393-398.
DONG G P, XIAO X D, ZHANG L L, et al.. Preparation and optical properties of red, green and blue afterglow electrospun nanofibers[J]. J. Mater. Chem., 2011, 21(7):2194.
CABELLO G, LILLO L, CARO C, et al.. Synthesis, characterization and optical properties of ATiO3-Pr thin films prepared by a photochemical method (where A=Ba and Ca)[J]. Mater. Res. Bull., 2015, 70:32-39.
CHEN R, CHEN D H. Enhanced luminescence properties of CaTiO3:Pr3+ phosphor with addition of SiO2 by solid-state reaction[J]. Spectrochim. Acta Part A:Mol. Biomol. Spectrosc., 2014, 127:256-260.
邾强强, 杨力勋, 季巍巍, 等. Si-N共掺对CaAl2O4:Eu2+和CaAl2O4:Eu2+,Sm3+荧光粉荧光和余辉性能的优化[J]. 中国稀土学报, 2013, 31(1):44-48. ZHU Q Q, YANG L X, JI W W, et al.. Optimization on photoluminescence and afterglow performance of CaAl2O4:Eu2+ and CaAl2O4:Eu2+, Sm3+ phosphors with Si-N Co-doping[J]. J. Chin. Rare Earth Soc., 2013, 31(1):44-48. (in Chinese)
ABRAGAM A, BLEANEY B. Electron Paramagnetic Resonance of Transition Ions[M]. London:Oxford University Press, 1970.
BOUTINAUD P, PINEL E, DUBOIS A P, et al.. UV-to-red relaxation pathways in CaTiO3:Pr3+[J]. J. Lumin., 2005, 111(1-2):69-80.
RIBEIRO G K, VICENTE F S, BERNARDI M I B, et al.. Short-range structure and photoluminescent properties of the CaTiO3:Pr, La phosphor[J]. J. Alloys Compd., 2016, 688:497-503.
GONALVES R F, LIMA A R F, GODINHO M J, et al.. Synthesis of Pr3+-doped CaTiO3 using polymeric precursor and microwave-assisted hydrothermal methods:a comparative study[J]. Ceram. Inter., 2015, 41:12841-12848.
OLIVEIRA L H, SAVIOLI J, MOURA A P, et al.. Investigation of structural and optical properties of CaTiO3 powders doped with Mg2+ and Eu3+ ions[J]. J. Alloys Compd., 2015, 647:265-275.
ZHENG H, BAGSHAW H, DE GYRGYFALVA G D C C, et al.. Raman spectroscopy and microwave properties of CaTiO3-based ceramics[J]. J. Appl. Phys., 2003, 94(5):2948-2956.
WANG Z W, SAXENA S K, ZHA C S. In situ X-ray diffraction and Raman spectroscopy of pressure-induced phase transformation in spinel Zn2TiO4[J]. Phys. Rev., 2002, 66:024103.
WANG Z W, LAZOR P, SAXENA S K, et al.. High-pressure raman spectroscopyic study of spinel (ZnCr2O4)[J]. J. Solid State Chem., 2002, 165:165-170.
ZHAO X K, FENDLER J H. Size quantization in semiconductor particulate films[J]. J. Phys. Chem., 1991, 95(9):3716-3723.
DEN EECKHOUT K V, SMET P F, POLEMAN D. Persistent luminescence in Eu2+-doped compounds:a review[J]. Materials, 2010, 3:2536-2566.
SAKAI R, KATSUMATA T, KOMURO S, et al.. Effect of composition on the phosphorescence from BaAl2O4:Eu2+, Dy3+ crystals[J]. J. Lumin., 1999, 85:149-154.
0
浏览量
56
下载量
2
CSCD
关联资源
相关文章
相关作者
相关机构