Y2O2S:Yb/Ho-silica/aminosilane core-shell nanoparticles were prepared by a solid-gas method in combination with polyvinylpyr-rolidone assisted one-step ammoniating method. The core was a single Y2O2S:Yb/Ho with 80 nm ...Y2O2S:Yb/Ho-silica/aminosilane core-shell nanoparticles were prepared by a solid-gas method in combination with polyvinylpyr-rolidone assisted one-step ammoniating method. The core was a single Y2O2S:Yb/Ho with 80 nm in diameter and the shell was silica/aminosilane with around 5 nm in thickness. The results of sedimentation experiment indicated that the nanoparticles could be well-dispersed in ethanol and water to form stable colloids. Since the coating weakened lattice vibration energies of the Y2O2S:Yb/Ho...展开更多
Under 980 nm laser excitation,red emission(5D0-7FJ(J=0,1,2)) of Eu3+ was observed in cubic Y2O3 codoped with Eu3+ and Yb3+.The dependence of the upconverted emission on doping concentration and laser power was studied...Under 980 nm laser excitation,red emission(5D0-7FJ(J=0,1,2)) of Eu3+ was observed in cubic Y2O3 codoped with Eu3+ and Yb3+.The dependence of the upconverted emission on doping concentration and laser power was studied.Yb3+ emission around 1000 nm(2F5/2-2F7/2) was reported upon excitation of Eu3+ ions.The decay curves of 5DJ(J=0,2) emission of Eu3+ under excitation of 266 nm pulse laser were examined to investigate the Eu3+→Yb3+ energy transfer process.Cooperative energy transfer process was discussed as the...展开更多
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
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
The photoluminescence （PL） property effect of Sc3＋ on the Er3＋/Y3＋/Yb3＋ doped Al2O3 powders prepared by sol-gel method has been investigated. The X-ray diffraction （XRD） and transmission electron microscopy （...The photoluminescence （PL） property effect of Sc3＋ on the Er3＋/Y3＋/Yb3＋ doped Al2O3 powders prepared by sol-gel method has been investigated. The X-ray diffraction （XRD） and transmission electron microscopy （TEM） implied that the distribution of dopants （Er3＋ , Y3＋ , Yb3＋ , Sc3＋） was improved effectively with the rise of Sc3＋ concentration. The Fourier transform infrared spectra （FTIR） results demonstrated that the ligand around the quenching center -OH and the population of -OH were altered by introducing different amounts of Sc3＋ . The PL intensity centered at 1530 nm was increasingly improved with the rise of Sc3＋ concentration, as well as the corresponding full widths at the half maximum （FWHM） and lifetime. The optimized PL intensity was 4.7 times higher than that non-Sc3＋ doped sample for the Al2O3 powders codoped with 10mol% Sc3＋ . This material can be promising candidates for optical fiber amplifier.展开更多
Long-lasting phosphor Y2O2S ： Eu^3＋ , Mg^2＋ , Ti^4＋ was synthesized by a flux method and their luminescence properties were investigated. The result indicates that the unit cell parameter c is linearly increased w...Long-lasting phosphor Y2O2S ： Eu^3＋ , Mg^2＋ , Ti^4＋ was synthesized by a flux method and their luminescence properties were investigated. The result indicates that the unit cell parameter c is linearly increased with the increase of Eu2O3 content in Y2O2S： Eu^3＋ （0.01 ≤ x ≤0.10）. On the other hand, the change of unit cell parameter a is not linear dependence. In the Y2O2S： Eu^3 ＋ crystal structure, Eu^3＋ ions only replaced Y^3 ＋ ions＇ places in which it posited center position of c axis. With the increase of Eu2O3 content, the position of the strongest emission peak changed from 540 nm （5D1→^ 7F2 transition） to 626 nm （^5Do→^7TF2 transition）, and the maximum intensity was obtained when x = 0.09 in Y2O2S： Eu^3＋ （0.01 ≤x ≤0.10）. This is due to the environment of trivalent europium in the crystal structure of Y2O2S. Doping with Mg^2＋ or Ti^4＋. ions alone cannot get the good long-lasting afterglow effect, whereas co-doping with Mg^2 ＋ and Ti^4 ＋ ions and excited with 365 nm ultraviolet light, a strong thermoluminesence peak appeared, red and orange long-lasting phosphorescence （LLP） was also observed and the phosphorescence lasted nearly 3 h in the light perception of the dark-adapted human eye （0.32 mcd·m^-2）. Thus the LLP mechanism was analyzed.展开更多
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
Y2O2S：Sm^3＋, Mg^2＋, Ti^4＋ phosphor was synthesized by co-precipitation method. The crystalline structure of all synthesized phosphors was investigated by XRD. The result showed that all synthesized phosphors had a...Y2O2S：Sm^3＋, Mg^2＋, Ti^4＋ phosphor was synthesized by co-precipitation method. The crystalline structure of all synthesized phosphors was investigated by XRD. The result showed that all synthesized phosphors had a hexagonal crystal structure, which was the same as Y2O2S. The emission spectrum and excitation spectrum were measured, and the effect of Sm^3 ＋ molar ratio on the spectra was discussed. The emission spectra of the phosphors showed three emission peaks due to typical transitions of Sm^3 ＋ （4G5/2→6HJ ,J = 5/2, 7/2, 9/2）, and the emission peaks at 606 nm was stronger than others. With the increase of Sm^3 ＋ molar ratio, the emission intensity was strengthened. The excitation peaks were ascribed to the representative energy transition 4f→4f of Ti^4＋ phosphor prepared by co-precipitation method was Sm^3＋ ions. The results indicated that the Y2O2S ： Sm^3＋ , Mg^2＋ , an efficient long afterglow phosphor.展开更多
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
A new Sm 3+ doped yttrium oxysulfide phosphor, which has the long-lasting phosphorescence, was synthesized by flux fusion method. The phosphors showed three typical transitions of Sm 3+ ( 4G 5/2→ 6H J, J=5/2,7/2,9/2)...A new Sm 3+ doped yttrium oxysulfide phosphor, which has the long-lasting phosphorescence, was synthesized by flux fusion method. The phosphors showed three typical transitions of Sm 3+ ( 4G 5/2→ 6H J, J=5/2,7/2,9/2), and the emission peaks located at 570, 606 and 659 nm respectively. A prominent luminescence and phosphorescence in orange-red can be seen in this phosphor when illuminated with UV light or visible light. The synthesized phosphors were characterized by X-ray diffraction, the excitation and photoluminescence spectra, and the after-glow intensity decay curve. The result shows that the Y 2O 2S∶ Sm 3+ phosphor is another efficient orange-red phosphor.展开更多
A new kind of doped rare earth free phosphor Y 2O 2S∶xTi (0<x≤0.10) with doped Ti as activative center was synthesized by solid state reaction and sintered at 1200 ℃ for 2.5 h under reducing atmosphere. XRD pa...A new kind of doped rare earth free phosphor Y 2O 2S∶xTi (0<x≤0.10) with doped Ti as activative center was synthesized by solid state reaction and sintered at 1200 ℃ for 2.5 h under reducing atmosphere. XRD patterns, photoluminescence spectra, time-resolved phosphorescence spectra and decay curves of the phosphor were investigated. XRD results reveal that a single Y 2O 2S phase exists with Ti content up to 6% (mol fraction). Yellow long lasting phosphorescence for present materials was observed in the dark with naked eye after the removal of the excitation light. From the time-resolved phosphorescence spectra the broad emission band centered at 565 nm was confirmed to be responsible for the long lasting phosphorescence which could maintain above 1 h. The possible mechanism responsible for the long lasting phosphorescence of the Y 2O 2S∶Ti phosphor was proposed.展开更多
基金Project supported by the National Natural Science Foundation of China (60979003 and 20977012)
文摘Y2O2S:Yb/Ho-silica/aminosilane core-shell nanoparticles were prepared by a solid-gas method in combination with polyvinylpyr-rolidone assisted one-step ammoniating method. The core was a single Y2O2S:Yb/Ho with 80 nm in diameter and the shell was silica/aminosilane with around 5 nm in thickness. The results of sedimentation experiment indicated that the nanoparticles could be well-dispersed in ethanol and water to form stable colloids. Since the coating weakened lattice vibration energies of the Y2O2S:Yb/Ho...
基金supported by the National Natural Science Foundation of China (10774140)Knowledge Project of the Chinese Academy of Sciences (KJCX2-YW-M11)+1 种基金Specialized Research Fund for the Doctoral Program of Higher Education (20060358054)Special Foundation for Talents of Anhui Province,China (2007Z021)
文摘Under 980 nm laser excitation,red emission(5D0-7FJ(J=0,1,2)) of Eu3+ was observed in cubic Y2O3 codoped with Eu3+ and Yb3+.The dependence of the upconverted emission on doping concentration and laser power was studied.Yb3+ emission around 1000 nm(2F5/2-2F7/2) was reported upon excitation of Eu3+ ions.The decay curves of 5DJ(J=0,2) emission of Eu3+ under excitation of 266 nm pulse laser were examined to investigate the Eu3+→Yb3+ energy transfer process.Cooperative energy transfer process was discussed as the...
基金Project supported by National Science Council of Taiwan (NSC98-2113-M-009-005-MY3)
文摘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.
基金Project supported by National Natural Science Foundation of China (20976002)Beijing Municipal Natural Science Foundation(2122012)+2 种基金Key Projects for Science and Technology of Beijing Education Commission (KZ201310011013)Project of Transformation and Industrialization of College Scientific & Technological AchievementsProjects of the Combination of Manufacture,Education & Research of Guangdong Province (2011B090400100)
文摘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.
基金supported by the Natural Science Foundation of Fujian Province (No. 2008J0146)
文摘The photoluminescence （PL） property effect of Sc3＋ on the Er3＋/Y3＋/Yb3＋ doped Al2O3 powders prepared by sol-gel method has been investigated. The X-ray diffraction （XRD） and transmission electron microscopy （TEM） implied that the distribution of dopants （Er3＋ , Y3＋ , Yb3＋ , Sc3＋） was improved effectively with the rise of Sc3＋ concentration. The Fourier transform infrared spectra （FTIR） results demonstrated that the ligand around the quenching center -OH and the population of -OH were altered by introducing different amounts of Sc3＋ . The PL intensity centered at 1530 nm was increasingly improved with the rise of Sc3＋ concentration, as well as the corresponding full widths at the half maximum （FWHM） and lifetime. The optimized PL intensity was 4.7 times higher than that non-Sc3＋ doped sample for the Al2O3 powders codoped with 10mol% Sc3＋ . This material can be promising candidates for optical fiber amplifier.
文摘Long-lasting phosphor Y2O2S ： Eu^3＋ , Mg^2＋ , Ti^4＋ was synthesized by a flux method and their luminescence properties were investigated. The result indicates that the unit cell parameter c is linearly increased with the increase of Eu2O3 content in Y2O2S： Eu^3＋ （0.01 ≤ x ≤0.10）. On the other hand, the change of unit cell parameter a is not linear dependence. In the Y2O2S： Eu^3 ＋ crystal structure, Eu^3＋ ions only replaced Y^3 ＋ ions＇ places in which it posited center position of c axis. With the increase of Eu2O3 content, the position of the strongest emission peak changed from 540 nm （5D1→^ 7F2 transition） to 626 nm （^5Do→^7TF2 transition）, and the maximum intensity was obtained when x = 0.09 in Y2O2S： Eu^3＋ （0.01 ≤x ≤0.10）. This is due to the environment of trivalent europium in the crystal structure of Y2O2S. Doping with Mg^2＋ or Ti^4＋. ions alone cannot get the good long-lasting afterglow effect, whereas co-doping with Mg^2 ＋ and Ti^4 ＋ ions and excited with 365 nm ultraviolet light, a strong thermoluminesence peak appeared, red and orange long-lasting phosphorescence （LLP） was also observed and the phosphorescence lasted nearly 3 h in the light perception of the dark-adapted human eye （0.32 mcd·m^-2）. Thus the LLP mechanism was analyzed.
基金Project supported by SRF for ROCS, SEM (2003-14), and Science and Technology Department of Zhejiang Province (2005C31019)
文摘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.
基金Project supported by the Hebei Developing Foundation of Science&Technology (51215103b)
文摘Y2O2S：Sm^3＋, Mg^2＋, Ti^4＋ phosphor was synthesized by co-precipitation method. The crystalline structure of all synthesized phosphors was investigated by XRD. The result showed that all synthesized phosphors had a hexagonal crystal structure, which was the same as Y2O2S. The emission spectrum and excitation spectrum were measured, and the effect of Sm^3 ＋ molar ratio on the spectra was discussed. The emission spectra of the phosphors showed three emission peaks due to typical transitions of Sm^3 ＋ （4G5/2→6HJ ,J = 5/2, 7/2, 9/2）, and the emission peaks at 606 nm was stronger than others. With the increase of Sm^3 ＋ molar ratio, the emission intensity was strengthened. The excitation peaks were ascribed to the representative energy transition 4f→4f of Ti^4＋ phosphor prepared by co-precipitation method was Sm^3＋ ions. The results indicated that the Y2O2S ： Sm^3＋ , Mg^2＋ , an efficient long afterglow phosphor.
基金Supported by the Project of the Combination of Industry and Research by the Ministry of Education of China and Guang-dong Province, China(No.0712226100023)
文摘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.
文摘A new Sm 3+ doped yttrium oxysulfide phosphor, which has the long-lasting phosphorescence, was synthesized by flux fusion method. The phosphors showed three typical transitions of Sm 3+ ( 4G 5/2→ 6H J, J=5/2,7/2,9/2), and the emission peaks located at 570, 606 and 659 nm respectively. A prominent luminescence and phosphorescence in orange-red can be seen in this phosphor when illuminated with UV light or visible light. The synthesized phosphors were characterized by X-ray diffraction, the excitation and photoluminescence spectra, and the after-glow intensity decay curve. The result shows that the Y 2O 2S∶ Sm 3+ phosphor is another efficient orange-red phosphor.
文摘A new kind of doped rare earth free phosphor Y 2O 2S∶xTi (0<x≤0.10) with doped Ti as activative center was synthesized by solid state reaction and sintered at 1200 ℃ for 2.5 h under reducing atmosphere. XRD patterns, photoluminescence spectra, time-resolved phosphorescence spectra and decay curves of the phosphor were investigated. XRD results reveal that a single Y 2O 2S phase exists with Ti content up to 6% (mol fraction). Yellow long lasting phosphorescence for present materials was observed in the dark with naked eye after the removal of the excitation light. From the time-resolved phosphorescence spectra the broad emission band centered at 565 nm was confirmed to be responsible for the long lasting phosphorescence which could maintain above 1 h. The possible mechanism responsible for the long lasting phosphorescence of the Y 2O 2S∶Ti phosphor was proposed.
