The long afterglow fluorescent material of M1-3xAl2O4:Eu2+ x/Dy3+2x(M2+= Sr2+, Ca2+ and Ba2+) phosphors are successfully synthesized by calcining precursor obtained via co-precipitation method at 1300oC for 4 h with r...The long afterglow fluorescent material of M1-3xAl2O4:Eu2+ x/Dy3+2x(M2+= Sr2+, Ca2+ and Ba2+) phosphors are successfully synthesized by calcining precursor obtained via co-precipitation method at 1300oC for 4 h with reducing atmosphere (20% H2 and 80% N2). The phase evolution, morphology and afterglow fluorescent properties are systematically studied by the various instruments of XRD, FE-SEM, PLE/PL spectroscopy and fluorescence decay analysis. The PL spectra shows that the Sr1-3xAl2O4:Eu2+x/Dy3+ 2x phosphors display vivid green emission at s519 nm (4f65d1!4f7 transition of Eu2+) with monitoring of the maximum excitation wavelength at s334 nm (8S7=2!6IJ transition of Eu2+), among which the optimal concentration of Eu2+ and Dy3+ is 15 at.% and 30 at.%, respectively. The color coordinates and temperature of Sr1-3xAl2O4:Eu2+ x/Dy3+ 2x phosphors are approximately at (s0.27, s0.57) and s6700 K, respectively. On the above basis, the M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors is obtained by the same method. The PL spectra of these phosphors shows the strongest blue emission at s440 nm and cyan emission at s499 nm under s334 nm wavelength excitation, respectively, which are blue shifted comparing to Sr1??3xAl2O4:Eu2+ x/Dy3+ 2x phosphors. The color coordinates and temperatures of M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors are approximately at (s0.18, s0.09), s2000 K and (s0.18, s0.42), s11600 K, respectively. In this work, long afterglow materials of green, blue and cyan aluminates phosphors with excellent properties have been prepared, in order to obtain wide application in the field of night automatic lighting and display.展开更多
A series samples of La0.6M0.4FeO3-δ （M = Ca, Sr, process （GNP）. FTIR, TG-DSC, XRD and TEM techniques Ba） perovskite-type oxides were prepared by glycine nitrate were used to characterize the chemical constitution...A series samples of La0.6M0.4FeO3-δ （M = Ca, Sr, process （GNP）. FTIR, TG-DSC, XRD and TEM techniques Ba） perovskite-type oxides were prepared by glycine nitrate were used to characterize the chemical constitution, thermal stability and phase structure. The electrical conductivity of the samples was investigated by four-probe technique. With the increase of substituted-ionic radius, the temperature of phase formation increases, and the solid solubility decreases gradually, respectively. The La0.6Ca0.4FeO3-δ（LCF）powder is pure cubic perovskite-type crystalline after fired at 850℃ for 2 h. The XRD patterns of La0.6Sr0.4FeO3-δ（LSF） powder shows a small quantity of SrO peaks sintered at 1050℃ for 2 h. The electrical conductivity of LCF and LSF at 500 - 800℃ is over 100 S·cm^ - 1, and the value of LCF is 1170 S·cm^ - 1 at 800℃, which indicate that LCF and LSF may be used as a profitable cathode for IT-SOFCs. The characteristic of La0.6 Ba0.4FeO3-δ（LBF） is poor, and the electrical conductivity at intermediate temperatures is 1/20 less than that of LSF.展开更多
Tunable and switchable Ba 0.5 Sr 0.5 TiO 3 film bulk acoustic resonators（FBARs） based on SiO 2 /Mo Bragg reflectors are explored,which can withstand high temperature for the deposition of Ba x Sr 1 x TiO 3（BST） fi...Tunable and switchable Ba 0.5 Sr 0.5 TiO 3 film bulk acoustic resonators（FBARs） based on SiO 2 /Mo Bragg reflectors are explored,which can withstand high temperature for the deposition of Ba x Sr 1 x TiO 3（BST） films at 800 C.The dc bias-dependent resonance may be attributed to the piezoelectricity of the BST film induced by an electrostrictive effect.The series resonant frequency is strongly dc bias-dependent and shifts downwards with dc bias increasing,while the parallel resonant frequency is only weakly dc bias-dependent and slightly shifts upwards at low dc bias（ 45 V） while downwards at higher dc bias.The calculated relative tunability of shifts at series resonance frequency is around 2.3% and the electromechanical coupling coefficient is up to approximately 8.09% at 60-V dc bias,which can be comparable to AlN FBARs.This suggests that a high-quality tunable BST FBAR device can be achieved through the use of molybdenum（Mo） as the high acoustic impedance layer in a Bragg reflector,which not only provides excellent acoustic isolation from the substrate,but also improves the crystallinity of BST films withstanding higher deposition temperature.展开更多
Ba0.6Sr0.4TiO3 （BST） thin films with and without HfO 2 buffer layer were fabricated on Pt/Ti/SiO2/Si substrates by pulsed laser deposition. Dependences of HfO 2 thickness on the dielectric property and leakage curre...Ba0.6Sr0.4TiO3 （BST） thin films with and without HfO 2 buffer layer were fabricated on Pt/Ti/SiO2/Si substrates by pulsed laser deposition. Dependences of HfO 2 thickness on the dielectric property and leakage current of BST thin films were focused. The dielectric constant of BST thin films increased and then decreased with the increase of HfO 2 thickness, while the dielectric relaxation was gradually improved. The loss tangent and leakage current under positive bias decreased with the HfO 2 thickness increasing. The leakage current analysis based on the Schottky emission indicated an improvement of the BST/Pt interface with HfO 2 buffer layer. The loss tangent, tunability and figure of merit of optimized HfO 2 buffered BST thin film achieved 0.009 8, 21.91% （E max = 200 kV/cm）, 22.40 at 10 6 Hz, respectively.展开更多
Ba0.6Sr0.4TiO3 (BST) thin films were fabricated on Pt coated Si (100) substrates by sol-gel techniques with molar ratio of (Ba+Sr) to Ti changing from 0.76 to 1.33. The effect of (Ba+Sr)/Ti ratio deviating from the st...Ba0.6Sr0.4TiO3 (BST) thin films were fabricated on Pt coated Si (100) substrates by sol-gel techniques with molar ratio of (Ba+Sr) to Ti changing from 0.76 to 1.33. The effect of (Ba+Sr)/Ti ratio deviating from the stoichiometry on microstructure, grain growth, dielectric and tunable properties of BST thin films were investigated. TiO2 and (Ba,Sr)2TiO4 were found as a second phase at the ratios of 0.76 and 1.33, respectively. The variation of the ratio reveals more significant effect on the grain size in B-site rich samples than that in A-site rich samples. The dissipation factor decreases rapidly from 0.1 to 0.01 at 1 MHz with decreasing (Ba+Sr)/Ti ratio. The tunability increases with decreasing ratio from 1.33 to 1.05, and then decreases with decreasing ratio from 1.05 to 0.76. The film with (Ba+Sr)/Ti ratio of 1.05 has a maximum tunability of 32% and a dissipation factor of 0.03 at 1 MHz.展开更多
(Ba0.3Sr0.7)x(Bi0.5Na0.5)1-xTiO3(BSxBNT,x=0.3–V0.8)ceramics were prepared to investigate their structure,dielectric and ferroelectric properties.BSxBNT ceramics possess pure perovskite structure accompanied from a te...(Ba0.3Sr0.7)x(Bi0.5Na0.5)1-xTiO3(BSxBNT,x=0.3–V0.8)ceramics were prepared to investigate their structure,dielectric and ferroelectric properties.BSxBNT ceramics possess pure perovskite structure accompanied from a tetragonal symmetry to pseudo-cubic one with the increase of x value,being confirmed by X-ray diffraction(XRD)and Raman results.The Tm corresponding to a temperature in the vicinity of maximum dielectric constant gradually decreases from 110℃(x=0.3)to-45℃(x=0.8),across Tm=36℃(x=0.5)with a maximum dielectric constant(ɛr=5920@1 kHz)around room temperature.The saturated polarization Ps gradually while the remnant polarization Pr sharply decreases with the increase of x value,making the P-E hysteresis loop of BSxBNT ceramics goes slim.A maximum difference between Ps and Pr(Ps-Pr)is obtained for BSxBNT ceramics with x=0.5,at which a high recoverable energy density(Wrec=1.04 J/cm3)is achieved under an applied electric field of 100 kV/cm with an efficiency ofη=77%.Meanwhile,the varied temperature P-E loops,fatigue measurements,and electric breakdown characteristics for the sample with x=0.5 indicate that it is promising for pulsed power energy storage capacitor candidate materials.展开更多
（Ba（0.6） Sr（0.4））（0.85） Bi（0.1） TiO3 ceramics doped with x wt%CaZrO3（x= 0-10） were synthesized by solid-state reaction method. The effects of CaZrO3 amount on the dielectric properties and structure of（Ba...（Ba（0.6） Sr（0.4））（0.85） Bi（0.1） TiO3 ceramics doped with x wt%CaZrO3（x= 0-10） were synthesized by solid-state reaction method. The effects of CaZrO3 amount on the dielectric properties and structure of（Ba（0.6）Sr（0.4））（0.85） Bi（0.1） TiO3 ceramics were investigated. X-ray diffraction results indicated a pure cubic perovskite structure for all samples and that the lattice parameter increased till x=5 and then slightly decreased. A homogenous microstructure was observed with the addition of CaZrO3. Dielectric measurements revealed a relaxor-like characteristic for all samples and that the diffusivity γ reached the maximum value of 1.78 at x=5. With the addition of CaZrO3, the dielectric constant dependence on electric field was weakened, insulation resistivity enhanced and dielectric breakdown strength improved obviously and reached 19.9 k V/mm at x=7.5. In virtue of low dielectric loss（tan d〈0.001 5）, moderate dielectric constant（er 〉1 500） and high breakdown strength（Eb 〉17.5 k V/mm）, the CaZrO3 doped（Ba（0.6）Sr（0.4））0.85 Bi（0.1） TiO3 ceramic is a potential candidate material for high power electric applications.展开更多
基金the National Natural Science Foundation of China (No. 51602126)the National Key Research and Development Plan of China (No. 2016YFB0303505)+1 种基金China and University of Jinan Postdoctoral Science Foundation (No. 2017M622118 and XBH1716)the 111 Project of International Corporation on Advanced Cement-based Materials (D17001).
文摘The long afterglow fluorescent material of M1-3xAl2O4:Eu2+ x/Dy3+2x(M2+= Sr2+, Ca2+ and Ba2+) phosphors are successfully synthesized by calcining precursor obtained via co-precipitation method at 1300oC for 4 h with reducing atmosphere (20% H2 and 80% N2). The phase evolution, morphology and afterglow fluorescent properties are systematically studied by the various instruments of XRD, FE-SEM, PLE/PL spectroscopy and fluorescence decay analysis. The PL spectra shows that the Sr1-3xAl2O4:Eu2+x/Dy3+ 2x phosphors display vivid green emission at s519 nm (4f65d1!4f7 transition of Eu2+) with monitoring of the maximum excitation wavelength at s334 nm (8S7=2!6IJ transition of Eu2+), among which the optimal concentration of Eu2+ and Dy3+ is 15 at.% and 30 at.%, respectively. The color coordinates and temperature of Sr1-3xAl2O4:Eu2+ x/Dy3+ 2x phosphors are approximately at (s0.27, s0.57) and s6700 K, respectively. On the above basis, the M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors is obtained by the same method. The PL spectra of these phosphors shows the strongest blue emission at s440 nm and cyan emission at s499 nm under s334 nm wavelength excitation, respectively, which are blue shifted comparing to Sr1??3xAl2O4:Eu2+ x/Dy3+ 2x phosphors. The color coordinates and temperatures of M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors are approximately at (s0.18, s0.09), s2000 K and (s0.18, s0.42), s11600 K, respectively. In this work, long afterglow materials of green, blue and cyan aluminates phosphors with excellent properties have been prepared, in order to obtain wide application in the field of night automatic lighting and display.
基金Project Supported bythe Natural Science Foundation of Bureau Education Anhui Province (N2004kj326)
文摘A series samples of La0.6M0.4FeO3-δ （M = Ca, Sr, process （GNP）. FTIR, TG-DSC, XRD and TEM techniques Ba） perovskite-type oxides were prepared by glycine nitrate were used to characterize the chemical constitution, thermal stability and phase structure. The electrical conductivity of the samples was investigated by four-probe technique. With the increase of substituted-ionic radius, the temperature of phase formation increases, and the solid solubility decreases gradually, respectively. The La0.6Ca0.4FeO3-δ（LCF）powder is pure cubic perovskite-type crystalline after fired at 850℃ for 2 h. The XRD patterns of La0.6Sr0.4FeO3-δ（LSF） powder shows a small quantity of SrO peaks sintered at 1050℃ for 2 h. The electrical conductivity of LCF and LSF at 500 - 800℃ is over 100 S·cm^ - 1, and the value of LCF is 1170 S·cm^ - 1 at 800℃, which indicate that LCF and LSF may be used as a profitable cathode for IT-SOFCs. The characteristic of La0.6 Ba0.4FeO3-δ（LBF） is poor, and the electrical conductivity at intermediate temperatures is 1/20 less than that of LSF.
基金Project supported by the National Natural Science Foundation of China (Grant Nos. 60871049 and 50972024)
文摘Tunable and switchable Ba 0.5 Sr 0.5 TiO 3 film bulk acoustic resonators（FBARs） based on SiO 2 /Mo Bragg reflectors are explored,which can withstand high temperature for the deposition of Ba x Sr 1 x TiO 3（BST） films at 800 C.The dc bias-dependent resonance may be attributed to the piezoelectricity of the BST film induced by an electrostrictive effect.The series resonant frequency is strongly dc bias-dependent and shifts downwards with dc bias increasing,while the parallel resonant frequency is only weakly dc bias-dependent and slightly shifts upwards at low dc bias（ 45 V） while downwards at higher dc bias.The calculated relative tunability of shifts at series resonance frequency is around 2.3% and the electromechanical coupling coefficient is up to approximately 8.09% at 60-V dc bias,which can be comparable to AlN FBARs.This suggests that a high-quality tunable BST FBAR device can be achieved through the use of molybdenum（Mo） as the high acoustic impedance layer in a Bragg reflector,which not only provides excellent acoustic isolation from the substrate,but also improves the crystallinity of BST films withstanding higher deposition temperature.
基金Project supported by the Foundation of the Education Commission of Shanghai Municipality (Grant Nos.07ZZ14, 08SG41)the National Natural Science Foundation of China (Grant No.50711130241)the Shanghai Rising Star Program (GrantNo.08QH14008)
文摘Ba0.6Sr0.4TiO3 （BST） thin films with and without HfO 2 buffer layer were fabricated on Pt/Ti/SiO2/Si substrates by pulsed laser deposition. Dependences of HfO 2 thickness on the dielectric property and leakage current of BST thin films were focused. The dielectric constant of BST thin films increased and then decreased with the increase of HfO 2 thickness, while the dielectric relaxation was gradually improved. The loss tangent and leakage current under positive bias decreased with the HfO 2 thickness increasing. The leakage current analysis based on the Schottky emission indicated an improvement of the BST/Pt interface with HfO 2 buffer layer. The loss tangent, tunability and figure of merit of optimized HfO 2 buffered BST thin film achieved 0.009 8, 21.91% （E max = 200 kV/cm）, 22.40 at 10 6 Hz, respectively.
基金Project (50332030) supported by the National Natural Science Foundation of China
文摘Ba0.6Sr0.4TiO3 (BST) thin films were fabricated on Pt coated Si (100) substrates by sol-gel techniques with molar ratio of (Ba+Sr) to Ti changing from 0.76 to 1.33. The effect of (Ba+Sr)/Ti ratio deviating from the stoichiometry on microstructure, grain growth, dielectric and tunable properties of BST thin films were investigated. TiO2 and (Ba,Sr)2TiO4 were found as a second phase at the ratios of 0.76 and 1.33, respectively. The variation of the ratio reveals more significant effect on the grain size in B-site rich samples than that in A-site rich samples. The dissipation factor decreases rapidly from 0.1 to 0.01 at 1 MHz with decreasing (Ba+Sr)/Ti ratio. The tunability increases with decreasing ratio from 1.33 to 1.05, and then decreases with decreasing ratio from 1.05 to 0.76. The film with (Ba+Sr)/Ti ratio of 1.05 has a maximum tunability of 32% and a dissipation factor of 0.03 at 1 MHz.
基金This work was financially supported by National Natural Science Foundation of China(51767010)Science&Technology Key Research Project of Jiangxi Provincial Education Department(GJJ170760)Graduate Student Innovation Fund of Jiangxi Province(YC2018-S295).
文摘(Ba0.3Sr0.7)x(Bi0.5Na0.5)1-xTiO3(BSxBNT,x=0.3–V0.8)ceramics were prepared to investigate their structure,dielectric and ferroelectric properties.BSxBNT ceramics possess pure perovskite structure accompanied from a tetragonal symmetry to pseudo-cubic one with the increase of x value,being confirmed by X-ray diffraction(XRD)and Raman results.The Tm corresponding to a temperature in the vicinity of maximum dielectric constant gradually decreases from 110℃(x=0.3)to-45℃(x=0.8),across Tm=36℃(x=0.5)with a maximum dielectric constant(ɛr=5920@1 kHz)around room temperature.The saturated polarization Ps gradually while the remnant polarization Pr sharply decreases with the increase of x value,making the P-E hysteresis loop of BSxBNT ceramics goes slim.A maximum difference between Ps and Pr(Ps-Pr)is obtained for BSxBNT ceramics with x=0.5,at which a high recoverable energy density(Wrec=1.04 J/cm3)is achieved under an applied electric field of 100 kV/cm with an efficiency ofη=77%.Meanwhile,the varied temperature P-E loops,fatigue measurements,and electric breakdown characteristics for the sample with x=0.5 indicate that it is promising for pulsed power energy storage capacitor candidate materials.
基金Funded by the National Natural Science Foundation of China(No.51302093)the Fundamental Research Funds for the Central Universities of China(Nos.2014TS046,2015MS017)
文摘（Ba（0.6） Sr（0.4））（0.85） Bi（0.1） TiO3 ceramics doped with x wt%CaZrO3（x= 0-10） were synthesized by solid-state reaction method. The effects of CaZrO3 amount on the dielectric properties and structure of（Ba（0.6）Sr（0.4））（0.85） Bi（0.1） TiO3 ceramics were investigated. X-ray diffraction results indicated a pure cubic perovskite structure for all samples and that the lattice parameter increased till x=5 and then slightly decreased. A homogenous microstructure was observed with the addition of CaZrO3. Dielectric measurements revealed a relaxor-like characteristic for all samples and that the diffusivity γ reached the maximum value of 1.78 at x=5. With the addition of CaZrO3, the dielectric constant dependence on electric field was weakened, insulation resistivity enhanced and dielectric breakdown strength improved obviously and reached 19.9 k V/mm at x=7.5. In virtue of low dielectric loss（tan d〈0.001 5）, moderate dielectric constant（er 〉1 500） and high breakdown strength（Eb 〉17.5 k V/mm）, the CaZrO3 doped（Ba（0.6）Sr（0.4））0.85 Bi（0.1） TiO3 ceramic is a potential candidate material for high power electric applications.
