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Upconversion luminescence of Gd2O3:Er3+and Gd2O3:Er3+/silica nanophosphors fabricated by EDTA combustion method 被引量:3
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作者 Le Quoc Minh Tran Kim Anh +6 位作者 Nguyen Duy Hung Pham Thi Minh Chau Nguyen Thi Quy Hai Ho Van Tuyen Vu Thi Thai Ha Vu Duc Tu Wieslaw Strek 《Journal of Rare Earths》 SCIE EI CAS CSCD 2019年第11期1126-1131,共6页
Gd2O3:Er^3+nanophosphors were fabricated by the combustion method in presence of Na2 ethylene diamine tetra acetic acid(EDTA-Na2)as fuel at not high temperature(≤350℃)within a very short time of 5 min.The added conc... Gd2O3:Er^3+nanophosphors were fabricated by the combustion method in presence of Na2 ethylene diamine tetra acetic acid(EDTA-Na2)as fuel at not high temperature(≤350℃)within a very short time of 5 min.The added concentration of Er^3+ions in Gd2O3 matrix was changed from 0.5 mol%to 5.0 mol%.The X-ray diffraction pattern of samples indicates the monoclinic structure of Gd2O3:Er^3+.The morphology and chemical composition analysis of the Gd2O3:Er^3+samples are characterized by a field emission scanning electron microscope(FESEM)and a Fourier-transform infrared spectrometer(FTIR).The photoluminescence(PL),photo luminescence excitation(PLE)and upconversion(UC)at room temperature of the prepared materials with different concentrations of Er^3+were investigated.The PL of Gd2O3:Er^3+nanomaterials are shown in visible at 545,594,623,648,688 nm under excitation at 275 nm.The emission bands from transitions of Er^3+from 2P3/2 to 4F9/2 are observed,UC luminescent spectra of the Gd2O3:Er^3+/silica nanocomposites under 976 nm excitation show the bands at 548 and 670 nm.The influence of excitation power at 980 nm for transitions were measured and calculated.The results indicate that the upconversion process of Gd2O3:Er^3+/silica is two photons absorption mechanism.The low temperature dependence of UC luminescent intensities of the main bands of Gd2O3:Er^3+was investigated towards development of a nanotemperature sensor in the range of 10-300 K. 展开更多
关键词 UPCoNVersIoN luminescence gd2o3:er3%PLUs% gd2o3:er3%PLUs%/silica NANophosphors EDTA combustion Rare earths
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Yellow upconversion luminescence in Ho^(3+)/Yb^(3+) co-doped Gd_2Mo_3O_9 phosphor 被引量:1
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作者 孙家跃 薛兵 +1 位作者 孙广超 崔殿鹏 《Journal of Rare Earths》 SCIE EI CAS CSCD 2013年第8期741-744,共4页
The strong yellow upconversion (UC) light emission was observed in Ho3+/yb3+ co-doped Gd2M0309 phosphor under the excitation of 980 nm diode laser. The phosphors were synthesized by the traditional solid-state rea... The strong yellow upconversion (UC) light emission was observed in Ho3+/yb3+ co-doped Gd2M0309 phosphor under the excitation of 980 nm diode laser. The phosphors were synthesized by the traditional solid-state reaction method. The structures of the samples were characterized by X-ray diffraction (XRD). Under 980 nm excitation, Ho3+/yb3+ co-doped Gd2Mo3O9 exhibited strong yellow UC emission based on the green emission near 541 nm generated by 5F4,5S2→5i8 transition and the strong red emission around 660 nm generated by 5F5→5I8 transition, which assigned to the intra-4f transitions of Ho3+ ions. The doping concentrations of Ho3+ and Yb3+ were determined to be 0.01 mol Ho3+ and 0.2 mol Yb3+ for the strongest yellow emission. Then the dependence of UC emis- sion intensity on excitation power density showed that the green and red UC emissions were involved in two-photon process. The possible UC mechanisms for the strong yellow emission were also investigated. The result indicated that this material was a promis- ing candidate for the application in the yellow display field. 展开更多
关键词 yellow upconversion phosphor gd2Mo3o9:Ho Yb rare earths
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Vacuum ultraviolet excited photoluminescence properties of Gd_2O_2CO_3:Eu^(3+) phosphor
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作者 王志龙 王育华 张加弛 《Journal of Rare Earths》 SCIE EI CAS CSCD 2008年第3期425-427,共3页
The Gd2O2CO3:Eu^3+ with type-Ⅱ structure phosphor was successfully synthesized via flux method at 400 ℃ and their photoluminescence properties in vacuum ultraviolet (VUV) region were examined. The broad and stro... The Gd2O2CO3:Eu^3+ with type-Ⅱ structure phosphor was successfully synthesized via flux method at 400 ℃ and their photoluminescence properties in vacuum ultraviolet (VUV) region were examined. The broad and strong excitation bands in the range of 153-205 nm owing to the CO3^2- host absorption and charge transfer (CT) of Gd^3+-O2^- were observed for Gd2O2CO3:Eu^3+. Under 172 nm excitation, Gd2O2CO3:Eu^3+ exhibited strong red emission with good color purity, indicating Eu^3+ ions located at low symmetry sites and the chromaticity coordination of luminescence for Gd2O2CO3:Eu^3+ was (x=0.652, y=0.345). The photoluminescence quenching concentration of Eu^3+ excited by 172 nm for Gd2O2CO3:Eu^3+ was about 5%. Gd2O2CO3:Eu^3+ would be a potential VUV-excited red phosphor applied in mercury-free fluorescent lamps. 展开更多
关键词 gd2o2Co3:Eu^3+ vacuum ultraviolet phosphor rare earths
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Synthesis and Luminescence Properties of Gd_2O_3∶Eu^(3+) Phosphors
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作者 李艳红 刘桂霞 洪广言 《Journal of Rare Earths》 SCIE EI CAS CSCD 2004年第1期70-74,共5页
Gd 2O 3∶Eu 3+ phosphors were prepared by urea homogeneous precipitation with different surfactant and sol-gel method. XRD patterns show that all the obtained samples are in cubic Gd 2O 3, and the results of FTIR... Gd 2O 3∶Eu 3+ phosphors were prepared by urea homogeneous precipitation with different surfactant and sol-gel method. XRD patterns show that all the obtained samples are in cubic Gd 2O 3, and the results of FTIR and fluorescent spectra conformed that OP is a good surfactant for preparing the Gd 2O 3∶Eu 3+ phosphors. The SEM photographs show that the particles prepared by urea homogeneous precipitation method are all spherical and well-dispersed, and grain morphology can be controlled by different surfactant. XRD and SEM indicate that the particle sizes prepared by sol-gel method are in the range of 5~30 nm, and the grain sizes increase with increasing of heated temperatures. Luminescence spectra indicat that the main emission peaks of all samples are at 610 nm, the intensities are different from samples prepared with different surfactant and the luminescence intensities increase with increasing of annealed temperatures. 展开更多
关键词 optics gd 2o 3∶Eu 3%PLUs% phosphors urea homogeneous precipitation sol-gel method luminescence spectra rare earths
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非等温动力学分析合成Gd_2O_2S∶Er的真空烧结过程 被引量:1
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作者 刘培培 王飞 杨斌 《有色金属工程》 CAS 北大核心 2019年第2期1-7,44,共8页
用不同升温速率下的热重(TG)和微分热重(DTG)技术研究固相反应法合成稀土掺杂硫氧化物(Gd_2O_2S∶Er)荧光粉的反应动力学,升温速率分别为5、10、15、20K/min。使用不同动力学分析方法对Gd_2O_2S∶Er的主要合成阶段进行动力学研究。用Kis... 用不同升温速率下的热重(TG)和微分热重(DTG)技术研究固相反应法合成稀土掺杂硫氧化物(Gd_2O_2S∶Er)荧光粉的反应动力学,升温速率分别为5、10、15、20K/min。使用不同动力学分析方法对Gd_2O_2S∶Er的主要合成阶段进行动力学研究。用Kissinger和Flynn-Wall-Ozawa法计算得到了各合成过程的动力学参数。Coats-Redfern法用于确定最可能的反应机理函数。通过分析TG和DTG曲线,得出常压/真空条件下合成Gd_2O_2S∶Er荧光粉的过程可分为三个阶段:失水、单质S与Na2CO3反应、Na2Sx与Gd2O3反应。通过计算发现,在真空条件下反应的活化能较低,表明真空条件有利于Gd_2O_2S∶Er的生成。真空条件下Gd_2O_2S∶Er荧光粉的合成为随机成核和随后生长控制机理,机理函数为g(α)=[-ln(1-α)]n。第二步控制过程的n值为2/3,第三步控制过程的n值为1/2。 展开更多
关键词 DTG gd2o2s∶er荧光粉 动力学 真空 合成
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Improvement of conversion efficiency of silicon solar cells using up-conversion molybdate La_2Mo_2O_9:Yb,R (R=Er, Ho) phosphors 被引量:6
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作者 陈彦吉 陈登铭 《Journal of Rare Earths》 SCIE EI CAS CSCD 2011年第8期723-726,共4页
The goal of this work was aimed to improve the power conversion efficiency of single crystalline silicon-based photovoltaic cells by using the solar spectral conversion principle, which employs an up-conversion phosph... The goal of this work was aimed to improve the power conversion efficiency of single crystalline silicon-based photovoltaic cells by using the solar spectral conversion principle, which employs an up-conversion phosphor to convert a low energy infrared photon to the more energetic visible photons to improve the spectral response. In this study, the surface of multicrystalline silicon solar cells was coated with an up-conversion molybdate phosphor to improve the spectral response of the solar cell in the near-infrared spectral range. The short circuit current (Isc), open circuit voltage (Voc), and conversion efficiency (η) of spectral conversion cells were measured. Preliminary experimental results revealed that the light conversion efficiency of a 1.5%–2.7% increase in Si-based cell was achieved. 展开更多
关键词 up-conversion phosphors La2Mo2o9:Yb3+ er3+ (Ho3+) solar cell rare earths
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Influence of annealing temperature on luminescent properties of Eu^(3+)/V^(5+) co-doped nanocrystalline Gd_2Ti_2O_7 powders 被引量:3
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作者 张盈 丁玲红 +1 位作者 庞新玲 张伟风 《Journal of Rare Earths》 SCIE EI CAS CSCD 2009年第6期900-904,共5页
Nanosized Gd2(1–x)Eu2xTi2O7:yV5+ phosphors were prepared via sol-gel method and characterized with X-ray diffraction,Raman spectroscopy,diffuse reflectance spectra and photoluminescence spectra.Their PL properties we... Nanosized Gd2(1–x)Eu2xTi2O7:yV5+ phosphors were prepared via sol-gel method and characterized with X-ray diffraction,Raman spectroscopy,diffuse reflectance spectra and photoluminescence spectra.Their PL properties were investigated as functions of the Eu3+ doping concentration and annealing temperature.The results indicated that the as-prepared samples showed a strong emission of Eu3+ under the irradiation of 303 nm.For Eu3+-doped Gd2Ti2O7,the orange emission at 586 nm was the strongest,which was correspond... 展开更多
关键词 photoluminescence gd2Ti2o7:Eu3%PLUs% V5%PLUs% phosphors sol-gel method rare earths
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Luminescence Characterization of Mg Doped Y_2O_2S:Ti Long Afterglow Phosphor 被引量:3
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作者 张朋越 洪樟连 +2 位作者 沈华翔 徐珍秀 樊先平 《Journal of Rare Earths》 SCIE EI CAS CSCD 2006年第z2期115-118,共4页
Y1.94-xMgxO2S:0.06Ti (0≤x≤0.10) phosphors with long afterglow were synthesized by solid state reaction route. The photoluminescence spectra, decay curves, thermoluminescent spectra and chromaticity coordinate curves... Y1.94-xMgxO2S:0.06Ti (0≤x≤0.10) phosphors with long afterglow were synthesized by solid state reaction route. The photoluminescence spectra, decay curves, thermoluminescent spectra and chromaticity coordinate curves were investigated. The results show that the luminescence intensity of Y1.94-xMgxO2S :0.06Ti (0≤x≤0. 10) phosphors decrease gradually with increasing Mg2+ ion content, and the shape of luminescence spectra and chromaticity coordinate change as well. Furthermore, two thermoluminescent peaks in single Ti-doped Y2O2S sample are found at 91.8 and 221.5℃, respectively. Nevertheless, significant different spectra were found for the Mg, Ti co-doped Y2O2S samples that three thermoluminescence peaks appear at 52.3, 141.7 and 226.8℃, respectively. These results indicate that the co-doped Mg ion changes the inherent trap depth of single Ti-doped Y2O2S: Ti phosphor, and induces simultaneously a new trap level in the Y1.94-xMgxO2S:0.06Ti phosphor. Based on the analysis of thermoluminescent spectra, photolumi-nescent spectra, decay curve and crystal structure defect, it was proposed that the varied structure defect and introduced new trap level by the doped Mg2+ ions should be responsible for reducing luminescence intensity and varying color in the Y1.94-x Mgx O2S : 0.06Ti phosphor. 展开更多
关键词 Y2o2s phosphor solid state reaction LUMINEsCENCE long afterglow rare earths
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Preparation of Gd_2O_2S:Pr Scintillation Ceramics by Pressureless Reaction Sintering Method 被引量:3
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作者 Jingbao Lian Xudong Sun +3 位作者 Tie Gao Qiang Li Xiaodong Li Zhigang Liu 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2009年第2期254-258,共5页
Fabrication of Gd2O2S:Pr scintillation ceramics by 2Gd2O3.(Gd,Pr)2(SO4)3.mH2O precursor was made Gd2O3, Pr6O11 and H2SO4 as the starting materials pressureless reaction sintering was investigated. The by hydrothe... Fabrication of Gd2O2S:Pr scintillation ceramics by 2Gd2O3.(Gd,Pr)2(SO4)3.mH2O precursor was made Gd2O3, Pr6O11 and H2SO4 as the starting materials pressureless reaction sintering was investigated. The by hydrothermal reaction using commercially available Then single phase Gd2O2SO4:Pr powder was obtained by calcining the precursor at 750℃ for 2 h. The Gd2O2SO4:Pr powder compacts can be sintered to single phase Gd2O2S:Pr ceramics with a relative density of 99% and mean grain size of 30um at 1750℃ for 2 h in flowing hydrogen atmosphere. Densification and microstructural development of the Gd2O2S:Pr ceramics were examined. Luminescence spectra of the Gd2O2S:Pr ceramic under 309 nm UV excitation and X-ray excitation show a green emission at 511 nm as the most prominent peak, which corresponds to the ^3p0-3H4 transition of Pr^3+ ions. 展开更多
关键词 scintillation ceramics gd2o2s Pressureless reaction sintering X-ray excited luminescence (XEL)
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Vacuum Ultraviolet Excited Photoluminescence Properties of Y_2O_2S:Eu^(3+),Bi^(3+) Phosphor 被引量:4
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作者 WANG Zhi-long WANG Yu-hua ZHANG Jia-chi 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2008年第6期679-682,共4页
As an Hg-free lamp using phosphor, the Bi^3+ and EH^3+ co-doped Y2O2S phosphors were prepared and their luminescence properties under vacuum ultraviolet(VUV) excitation were investigated. The VUV photoluminescent ... As an Hg-free lamp using phosphor, the Bi^3+ and EH^3+ co-doped Y2O2S phosphors were prepared and their luminescence properties under vacuum ultraviolet(VUV) excitation were investigated. The VUV photoluminescent intensity of Y2O2S:Eu^3+ was weak, however, considerably stronger red emission at 626 nm with good color purity was observed in Y2O2S:Eu^3+,Bi^3+ systems. Investigation on the photoluminescence reveals that the strong VUV luminescence of Y2O2S:Eu^3+,Bi^3+ at 147 nm is mainly because the Bi^3+ acts as a medium and effectively performs the energy transfer process: Y^3+-O^2-→Bi^3+→Eu^3+, while the intense emission band at 172 nm is attributed to the absorption of the characteristic ^1So-^1P1 transition of Bi^3+ and the direct energy transfer from Bi^3+ to Eu^3+. The Y2O2S:Eu^3+,Bi^3+ shows excellent VUV optical properties compared with the commercial (Y,Gd)BO3:Eu^3+. Thus, the Y2O2S:Eu^3+,Bi^3+ can be a potential red VUV-excited candidate applied in Hg-free lamps for backlight of liquid crystal display. 展开更多
关键词 Y2o2s:Eu^3+ Bi^3+ Vacuum ultraviolet(VUV) phosphor
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Study on analysis of crystal structure in CeO_2 doped with Er_2O_3 or Gd_2O_3 被引量:1
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作者 Yuki Tahara Kazufumi Yasunaga +2 位作者 Toshiyuki Matsui Fuminobu Hori Akihiro Iwase 《Journal of Rare Earths》 SCIE EI CAS CSCD 2010年第S1期164-167,共4页
To simulate the effects of burnable poison doping in nuclear fuel UO2,Er2O3(or Gd2O3)-doped CeO2 pellets were prepared. Changes in lattice constant and atomic disordering for CeO2 due to the Er2O3 and Gd2O3 doping wer... To simulate the effects of burnable poison doping in nuclear fuel UO2,Er2O3(or Gd2O3)-doped CeO2 pellets were prepared. Changes in lattice constant and atomic disordering for CeO2 due to the Er2O3 and Gd2O3 doping were measured by means of XRD and XAFS. By the Er2O3 doping,the lattice constant decreased,and a disordering of lattice structure was induced in the samples. The doping with Er2O3 also induced the disordering of atomic arrangement around Er atoms,which was observed through the change in XAFS spectra. In contrast,the effect of Gd2O3 doping was smaller than that of Er2O3 doping. The result was discussed in terms of ionic size of dopants in CeO2 crystal. 展开更多
关键词 Ceo2 ceramic pellets er2o3 and gd2o3 doping Change in lattice structure XRD XAFs rare earths
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微波法合成红色长余辉发光材料Gd_2O_2S∶Eu,Mg,Ti及其发光特性 被引量:11
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作者 翟永清 刘元红 +1 位作者 孟媛 张少阳 《光谱学与光谱分析》 SCIE EI CAS CSCD 北大核心 2007年第4期634-638,共5页
用微波辐射法首次合成了Gd2O2S∶Eu,Mg,Ti红色磷光化合物,用X射线粉末衍射(XRD)、扫描电镜(SEM)、荧光分光光度计等对合成产物进行了分析和表征。结果表明:材料的晶体结构为六方晶系,与Gd2O2S的相同。颗粒的形貌为类球形,分散性较... 用微波辐射法首次合成了Gd2O2S∶Eu,Mg,Ti红色磷光化合物,用X射线粉末衍射(XRD)、扫描电镜(SEM)、荧光分光光度计等对合成产物进行了分析和表征。结果表明:材料的晶体结构为六方晶系,与Gd2O2S的相同。颗粒的形貌为类球形,分散性较好,尺寸在1-2μm之间。Gd2O2S∶Eu,Mg,Ti的激发光谱呈带状,激发光谱主峰位于360nm,另外在400,422,472nm等处也有激发峰存在;发射光谱为线状光谱,归属于Eu^3+的5^DJ(J=0,1,2)到7^FJ(J=0,1,2,3,4)的跃迁。随着Eu浓度的增加,位于蓝绿区的586,557,541,513,498,471,468nm处的发射峰逐渐减弱,而主峰位于627nm处的红光发射明显增强。当Eu浓度为6mol%时,红光发射最强。Mg,Ti共掺杂可显著改善其余辉性质。 展开更多
关键词 gd2o2s Eu Mg Ti 微波法 激发光谱 发射光谱 长余辉
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掺杂离子对Gd_2O_2S:Eu^(3+)磷光体结构和发光性能的影响 被引量:7
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作者 王飞 刘大春 +2 位作者 杨斌 刘利军 戴永年 《中国有色金属学报》 EI CAS CSCD 北大核心 2012年第4期1107-1112,共6页
采用高温固相反应法制备出新型红色长余辉发光材料Gd2O2S:Eu3+,Xn+(X为Mg、Si、Ti中的一种或两种),研究掺杂离子对Gd2O2S:Eu3+磷光体的晶体结构、形貌粒度和发光性能的影响。通过X射线粉末衍射(XRD)、扫描电镜(SEM)和分光光度计等对合... 采用高温固相反应法制备出新型红色长余辉发光材料Gd2O2S:Eu3+,Xn+(X为Mg、Si、Ti中的一种或两种),研究掺杂离子对Gd2O2S:Eu3+磷光体的晶体结构、形貌粒度和发光性能的影响。通过X射线粉末衍射(XRD)、扫描电镜(SEM)和分光光度计等对合成产物进行分析与表征。结果表明:掺杂离子没有改变Gd2O2S:Eu3+磷光体的晶体结构,颗粒的形貌为类球形,分散性良好。同时,掺杂离子显著地延长发光材料Gd2O2S:Eu3+的余辉时间,并显示纯正的红色发光。 展开更多
关键词 gd2o2s:Eu3%PLUs% 磷光体 掺杂离子 光谱
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助熔剂法合成Gd_2O_2S∶Tb荧光粉 被引量:10
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作者 王飞 张金朝 宋鹂 《华东理工大学学报(自然科学版)》 EI CAS CSCD 北大核心 2006年第8期943-947,共5页
采用共沉淀法制备前驱体,再加入助熔剂煅烧合成Gd2O2S∶Tb荧光粉,并对制备的荧光粉样品的晶体结构及发光性能进行了系统研究。结果表明:助熔剂的选择对Gd2O2S∶Tb荧光粉合成影响显著;当L i2CO3与L i3PO4添加量的摩尔比为2∶1时发光亮度... 采用共沉淀法制备前驱体,再加入助熔剂煅烧合成Gd2O2S∶Tb荧光粉,并对制备的荧光粉样品的晶体结构及发光性能进行了系统研究。结果表明:助熔剂的选择对Gd2O2S∶Tb荧光粉合成影响显著;当L i2CO3与L i3PO4添加量的摩尔比为2∶1时发光亮度最大,且颗粒分布较均匀;当助熔剂的质量分数为0.35时发光性能最好。 展开更多
关键词 荧光粉 gd2o2s:Tb 助熔剂 晶体结构 发光性能
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固相合成Gd_2O_2S:Pr陶瓷闪烁体粉末 被引量:7
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作者 黄存新 刘翠 +4 位作者 余明清 袁家铮 范仕刚 赵春霞 李建保 《人工晶体学报》 EI CAS CSCD 北大核心 2005年第1期79-83,69,共6页
本文采用固相反应合成Gd2O2S:Pr陶瓷闪烁体粉末,确定了固相反应时Gd2O3 与S的配比分别约为Gd2O3与S总质量的 88%和 12%,并往其中成功地掺入了痕量Pr2O3,测量了GOS:Pr的荧光光谱,分析表明,制备出的GOS:Pr粉末的主发射峰位于 512nm处,与... 本文采用固相反应合成Gd2O2S:Pr陶瓷闪烁体粉末,确定了固相反应时Gd2O3 与S的配比分别约为Gd2O3与S总质量的 88%和 12%,并往其中成功地掺入了痕量Pr2O3,测量了GOS:Pr的荧光光谱,分析表明,制备出的GOS:Pr粉末的主发射峰位于 512nm处,与硅光电二极管光谱感光度匹配。此法制备出的GOS:Pr粉末适于制造GOS:Pr闪烁陶瓷。 展开更多
关键词 gd2o2s:Pr 陶瓷闪烁体 固相反应合成 荧光光谱
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痕量双掺Sm^(3+)和Gd^(3+)对Y_2O_2S∶Eu^(3+)发光特性的影响 被引量:5
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作者 袁剑辉 袁红辉 +2 位作者 张振华 程玉民 王晓君 《中国稀土学报》 CAS CSCD 北大核心 2005年第4期421-424,共4页
通过对Y2O2S∶Eu3+红色荧光粉痕量引入Sm3+和Gd3+的研究,发现可有效地增强发光强度,明显改善其电压特性(发射强度与激发电压间的关系特性),且不影响材料的其他物理化学性能。讨论和分析了发射强度增强、电压特性改善的原因:Gd3+对Y3+的... 通过对Y2O2S∶Eu3+红色荧光粉痕量引入Sm3+和Gd3+的研究,发现可有效地增强发光强度,明显改善其电压特性(发射强度与激发电压间的关系特性),且不影响材料的其他物理化学性能。讨论和分析了发射强度增强、电压特性改善的原因:Gd3+对Y3+的置换,减少了因Eu3+对Y3+置换所引起的晶格的畸变、缺陷,使Eu3+离子晶场环境得到改善,从而减弱了无辐射过程及因晶格畸变所造成的能量损失;Sm3+的发射与Eu3+的吸收(激发)的部分重叠,且Eu3+激发光谱中包含有Sm3+激发跃迁谱线,导致了Sm3+→Eu3+共振能量传递可能性,有效地实现Sm3+对Eu3+的敏化效应。 展开更多
关键词 发光学 sm3%PLUs%∶gd3%PLUs%共掺 Y2o2s∶Eu3%PLUs% 发光增强 耐压性提高 稀土
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(Gd1-x,Prx)2O2S闪烁陶瓷粉体的合成及光致发光研究 被引量:3
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作者 连景宝 李晓东 +3 位作者 高铁 刘志刚 李继光 孙旭东 《功能材料》 EI CAS CSCD 北大核心 2008年第5期713-716,共4页
以Gd2O3、Pr6O11和H2SO4为原料,通过H2还原法合成不同浓度Pr3+离子掺杂的(Gd1-x,Prx)2O2S闪烁陶瓷粉体。利用DTA-TG-DTG、FT-IR、XRD、SEM、光致发光(PL)光谱等测试手段对合惩的粉体进行了表征。研究表明,将Gd2O3和Pr6O11与稀H2SO4在10... 以Gd2O3、Pr6O11和H2SO4为原料,通过H2还原法合成不同浓度Pr3+离子掺杂的(Gd1-x,Prx)2O2S闪烁陶瓷粉体。利用DTA-TG-DTG、FT-IR、XRD、SEM、光致发光(PL)光谱等测试手段对合惩的粉体进行了表征。研究表明,将Gd2O3和Pr6O11与稀H2SO4在100℃加热搅拌,制备出2Gd2O3.(Gd1-x,Prx)2(SO4)3.12 H2O前躯体。前驱体在750℃煅烧2h可获得(Gd1-x,Prx)2O2SO4粉体,该粉体在H2气氛下750℃还原1h可以转化为具有疏松和多孔蜂窝状结构的单相(Gd1-x,Prx)2O2S闪烁陶瓷粉体。(Gd1-x,Prx)2O2S粉体在307nm的紫外光激发下呈现绿光发射,主发射峰位于511nm,归属于Pr3+离子的3P0-3H4跃迁。发光强度随Pr3+离子浓度的变化而变化,当Pr3+离子的摩尔分数为1.000%时,粉体具有最高的发光强度。 展开更多
关键词 gd2o2s 闪烁陶瓷 H2还原法 光致发光
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Gd_2O_3:Yb^(3+),Er^(3+)上转换纳米纤维的制备与表征 被引量:2
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作者 王进贤 刘莉 +1 位作者 董相廷 刘桂霞 《红外与毫米波学报》 SCIE EI CAS CSCD 北大核心 2010年第1期10-14,56,共6页
采用溶胶-凝胶法与静电纺丝技术相结合制备了PVA/[Gd(NO3)3+Yb(NO3)3+Er(NO3)3]复合纳米纤维,将其进行热处理,得到Gd2O3:Yb3+,Er3+上转换纳米纤维.采用XRD、SEM、TG-DTA、FTIR和荧光光谱对样品进行了表征.结果表明:复合纳米纤维为无定型... 采用溶胶-凝胶法与静电纺丝技术相结合制备了PVA/[Gd(NO3)3+Yb(NO3)3+Er(NO3)3]复合纳米纤维,将其进行热处理,得到Gd2O3:Yb3+,Er3+上转换纳米纤维.采用XRD、SEM、TG-DTA、FTIR和荧光光谱对样品进行了表征.结果表明:复合纳米纤维为无定型,Gd2O3:Yb3+,Er3+上转换纳米纤维属于体心立方晶系,空间群为Ia3.复合纳米纤维的平均直径约为140nm,经过600℃焙烧后,获得了直径约60nm的Gd2O3:Yb3+,Er3+上转换纳米纤维.当焙烧温度高于600℃时,复合纳米纤维中水分、有机物和硝酸盐分解挥发完毕,样品不再失重,总失重率为81%.复合纳米纤维的红外光谱与纯PVA的红外光谱一致,600℃以上时,生成了Gd2O3:Yb3+,Er3+上转换纳米纤维.该纤维在980nm激光激发下发射出中心波长为522nm、560nm的绿色和659nm的红色上转换荧光,对应于Er3+离子的2H11/2/4S3/2→4Il5/2跃迁和4F9/2→4Il5/2跃迁.在Gd2O3:Yb3+,Er3+上转换纳米纤维形成过程中,PVA分子起到了导向模板作用.PVA/[Gd(NO3)3+Yb(NO3)3+Er(NO3)3]复合纳米纤维在热处理过程中,PVA分解挥发,稀土硝酸盐分解并氧化生成Gd2O3:Yb3+,Er3+纳米颗粒,这些纳米颗粒相互联结起来形成了Gd2O3:Yb3+,Er3+上转换纳米纤维. 展开更多
关键词 gd2o3 gd2o3:Yb3%PLUs% er3%PLUs% 纳米纤维 上转换
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微波法合成新型红色长余辉材料Gd_2O_2S:Eu,Mg,Ti中助熔剂的影响 被引量:7
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作者 翟永清 刘元红 《人工晶体学报》 EI CAS CSCD 北大核心 2006年第4期871-875,共5页
用微波辐射法合成了红色长余辉材料Gd2O2S:Eu,Mg,Ti,用X射线粉末衍射(XRD)、扫描电镜(SEM)、荧光分光光度计等手段对合成产物进行了分析和表征,并研究了不同助熔剂L i2CO3,Na2CO3,K2CO3,Na3PO4,KH2PO4以及L i2CO3和Na2CO3共同作用对材... 用微波辐射法合成了红色长余辉材料Gd2O2S:Eu,Mg,Ti,用X射线粉末衍射(XRD)、扫描电镜(SEM)、荧光分光光度计等手段对合成产物进行了分析和表征,并研究了不同助熔剂L i2CO3,Na2CO3,K2CO3,Na3PO4,KH2PO4以及L i2CO3和Na2CO3共同作用对材料的微观形貌及发光性能的影响。结果表明:不同的助熔剂的加入均可得到单相晶体,材料的晶体结构为六方晶系,与Gd2O2S的相同。颗粒分散性较好,晶粒尺寸以及形貌因助熔剂的不同而有所差别。发光性质研究表明:不同助熔剂的加入并没有改变样品发射谱主峰位置(627nm),但对其峰强度产生明显影响,激发光谱中的情况与此相似。研究发现L i2CO3和Na2CO3共同作用可有效延长余辉时间。 展开更多
关键词 助熔剂 gd2o2s:Eu Mg Ti 微波法 光谱 长余辉
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ZnO掺杂对Gd_2O_2S∶Tb晶体结构及发光性能的影响 被引量:2
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作者 王飞 张金朝 宋鹂 《稀有金属》 EI CAS CSCD 北大核心 2007年第5期661-665,共5页
采用共沉淀法制备前驱体,通过固相反应制备了Gd2O2S∶Tb荧光粉。结果表明,采用氧化锌的掺杂,提高了荧光体的发光性能。选择合适的Zn2+浓度,可以通过控制焙烧条件,控制其粒径分布,使晶型趋于完整;通过对XRD和光谱的分析,可以清楚看出ZnO... 采用共沉淀法制备前驱体,通过固相反应制备了Gd2O2S∶Tb荧光粉。结果表明,采用氧化锌的掺杂,提高了荧光体的发光性能。选择合适的Zn2+浓度,可以通过控制焙烧条件,控制其粒径分布,使晶型趋于完整;通过对XRD和光谱的分析,可以清楚看出ZnO的添加,并未产生新相,而是使晶胞变小,使Gd3+与Tb3+以及Tb3+之间更容易发生能量传递,增强Tb3+离子的自敏化作用,加强5D4—7Fj发射,猝灭5D3—7Fj的发射,在提高发光亮度的同时,提高了荧光粉的色纯度。 展开更多
关键词 gd2o2s2Tb 氧化锌 晶体结构 发光性能
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