The dielectric properties and phase transition characteristics of La2O3- and Sb2O3-doped barium strontium titanate ceramics prepared by solid state route were investigated. The microstructure was identified by X-ray d...The dielectric properties and phase transition characteristics of La2O3- and Sb2O3-doped barium strontium titanate ceramics prepared by solid state route were investigated. The microstructure was identified by X-ray diffraction method and scanning electron microscope was also employed to observe the surface morphologies. It is found that （La,Sb）-codoped barium strontium titanate ceramics exhibit typical perovskite structure and the average grain size decreases dramatically with increasing the content of Sb2O3. Both La3＋ ions and Sb3＋ ions occupy the A-sites in perovskite lattice. The dielectric constant and dielectric loss of barium strontium titanate based ceramics are obviously influenced by La2O3 as well as Sb2O3 addition content. The tetragonal-cubic phase transition of La2O3 modified barium strontium titanate ceramics is of second order and the Curie temperature shifts to lower value with increasing the La2O3 doping content. The phase transition of （La,Sb）-codoped barium strontium titanate ceramics diffuses and the deviation from Curie-Weiss law becomes more obvious with the increase in Sb2O3 concentration. The temperature corresponding to the dielectric constant maximum of （La,Sb）-codoped barium strontium titanate ceramics decreases with increasing the Sb2O3 content, which is attributed to the replacement of host ions by the Sb3＋ ions.展开更多
The microstructures and dielectric properties of Sb2O3-doped Ti deficient barium strontium titanate ceramics prepared by solid state method were investigated with non-stoichiometric level and Sb2O3content by SEM,XRD a...The microstructures and dielectric properties of Sb2O3-doped Ti deficient barium strontium titanate ceramics prepared by solid state method were investigated with non-stoichiometric level and Sb2O3content by SEM,XRD and LCR measure system.It is found that with the increase ofδ,(Ba0.75Sr0.25)Ti1-δO3-2δceramics transform from single phase solid solutions with typical cubic perovskite structure to multiphase compounds while(Ba0.75Sr0.25)Ti0.998O2.996ceramics remain to be single-phase with the increasing Sb2O3content.The distortion of the ABO3perovskite lattice caused by VTi″″and VO..induces the drop of Curie temperature and the rise of relative dielectric constant in(Ba0.75Sr0.25)Ti1-δO3-2δceramics with increasingδvalue.The orientation of VO??elastic dipoles results in the domain-wall pinning and thus the reduction of the dielectric loss.With increasing Sb2O3content,the relative dielectric constant,dielectric constant maximum and Curie temperature of(Ba0.75Sr0.25)Ti0.998O2.996ceramics decrease dramatically while the dielectric loss increases.展开更多
A glass with composition of B_(2)O_(3)-Bi_(2)O_(3)-SiO_(2)-CaO-BaO-Al_(2)O_(3)-ZrO_(2)(BBSZ)modified Ba_(x)Sr_(1-x)TiO_(3)(BST,x=0.3 and 0.4)ceramics were prepared by a conventional solid state reaction method abided ...A glass with composition of B_(2)O_(3)-Bi_(2)O_(3)-SiO_(2)-CaO-BaO-Al_(2)O_(3)-ZrO_(2)(BBSZ)modified Ba_(x)Sr_(1-x)TiO_(3)(BST,x=0.3 and 0.4)ceramics were prepared by a conventional solid state reaction method abided by a formula of BST+y%BBSZ(y=0,2,4,7,and 10,in mass).The effect of BBSZ glass content on the structure,dielectric properties and energy storage characteristics of the ceramics was investigated.The dielectric constant reduced but the endurable electrical strength enhanced due to the BBSZ glass addition in BST ceramics.In particular,the dielectric loss of the ceramics at elevated temperature(e.g.200℃)can be strongly suppressed from tanδ>20%to tanδ<3% after BBSZ glass modification.For Ba_(0.3)Sr_(0.7)TiO_(3)+2%BBSZ ceramics,an optimized energy storage density(γ=0.63 J/cm^(3))and efficiency(η=91.6%)under an applied electric field of 160 kV/cm was obtained at room temperature.Meanwhile,the temperature dependent polarization-electric field(P-E)hysteresis loops were measured to evaluate the energy storage characteristics of the ceramics potential for high voltage capacitor application at elevated temperatures.展开更多
The influence of the composition （Yb2O3, MgO, CeO2, Li2CO3） on the dielectric properties of medium temperature sintering （Ba, Sr）TiO3 （BST） series capacitor ceramics was investigated by means of conventional tec...The influence of the composition （Yb2O3, MgO, CeO2, Li2CO3） on the dielectric properties of medium temperature sintering （Ba, Sr）TiO3 （BST） series capacitor ceramics was investigated by means of conventional technology process and orthogonal design experiments. The major secondary influencing factors and the influencing tendency of various factor＇s levels for the dielectric properties of BST ceramics were obtained. The optimum formula for maximum dielectric constant （ε） and for minimum dielectric loss （tanδ） was obtained under the experimental conditions. The BST ceramics with optimum comprehensive properties was obtained by means of orthogonal design experiments, with the sintering temperature at 1200 ℃, the dielectric constant 5239, the dielectric loss 0.0097, withstand electric voltage over 6 MV·m^-1, capacitance temperature changing ence of various components on the providing the basis for preparation rate （△C/C） - 75.67%, and suited for Y5V character. The mechanism of the infludielectric properties of medium temperature sintering BST ceramics was studied, thus of multilayer capacitor ceramics and single-chip capacitor ceramics.展开更多
The effect of Yb2O3 doping amount on the dielectric properties of (Ba, Sr)TiO3 (BST) series capacitor ceramics prepared using solid state reaction method were studied. With the increasing of Yb2O3 doping amount, the d...The effect of Yb2O3 doping amount on the dielectric properties of (Ba, Sr)TiO3 (BST) series capacitor ceramics prepared using solid state reaction method were studied. With the increasing of Yb2O3 doping amount, the dielectric constant(ε) of materials increased, the dielectric loss(tanδ) of materials decreased to minimum when w(Yb2O3) was 0.9%. The BST ceramics with high ε(10000), low tanδ(0.0213) and high DC breakdown voltage(7.2 kV·mm-1) were obtained. The influence of Yb2O3 doping amount on the structure of BST ceramics was studied by means of X-ray diffraction(XRD) and scanning electron microscope. The influencing mechanism of Yb2O3 on the dielectric properties of BST ceramics was studied. The results showed that Yb2O3 doping influenced the properties and structure of BST ceramics by means of forming defect solid solution, but did not influence crystal grain size,the crystal phase was single perovskite structure, did not influence XRD data of BST and did not improve capacitance temperature property greatly, but increase dielectric constant greatly. These results provided the basis for Yb2O3-doped BST series capacitor ceramics.展开更多
In order to explore new application opportunities of Barium Strontium Titanate (BST) ceramic composite by modifying the conventional ferroelectric properties of BST through La<sub>2</sub>O<sub>3</...In order to explore new application opportunities of Barium Strontium Titanate (BST) ceramic composite by modifying the conventional ferroelectric properties of BST through La<sub>2</sub>O<sub>3</sub> doping in BST matrix sintered at different temperature was investigated in this current study. Unadulterated Ba<sub>0.3</sub>Sr<sub>0.7</sub>TiO<sub>3</sub> (BST) matrix was prepared from BaTiO<sub>3</sub> (99.95%) and SrTiO<sub>3</sub> (99.95%) taken in stoichiometric extents which later doped by La<sub>2</sub>O<sub>3</sub> (99.99%) in varying extents (0.05 g, 0.10 g and 0.15 g) exploiting solid state reaction route. Doping caused drag effect for the penetration of impurities and sintering temperature helped the impurities migration to BST. Dielectric constant gets lower with rising of frequency, as electrons do not get enough time to polarize at high frequency. Dielectric constant and conductance are found maximum for the sample (0.1 g La<sub>2</sub>O<sub>3</sub> doped BST) sintered at 1460<span style="white-space:nowrap;">°</span>C and reverse is found in impedance analysis. These electrical properties showed visible frequency dependent response irrespective of sintering temperature and doping.展开更多
Composite ceramics of 0.7BaO·0.3SrO·(1-y)TiO2·yNb2O5 (BSTN) with coexistence of barium strontium titanate, Ba1-xSrxTiO3 (BST), and strontium barium niobate, SrxBa1-xNb2O6 (SBN) phases were successfully ...Composite ceramics of 0.7BaO·0.3SrO·(1-y)TiO2·yNb2O5 (BSTN) with coexistence of barium strontium titanate, Ba1-xSrxTiO3 (BST), and strontium barium niobate, SrxBa1-xNb2O6 (SBN) phases were successfully prepared in situ by controlling excess components according to a specially designed formula of 0.7BaO·0.3SrO·(1-y)TiO2·yNb2O5 and by using a traditional ceramic process. X-ray diffractometry (XRD), scanning electron microscopy (SEM) and energy dispersion spectrometer (EDS) were used to characterize the phase composition, morphology and the micro-area chemical composition of the composite ceramics. The results showed that the SBN tungsten bronze phase appeared and coexisted stably with the BST perovskite phase when the excess content of Nb2O5 was >6mol%, whereas the BST perovskite phase formed and coexisted stably with the SBN tungsten bronze phase when the excess content of TiO2 was >5.3mol%. In the case of the two phases being equivalent to each other in BSTN composite ceramics, Nb2O5 was hard to be resolved into the perovskite phase, however, a few of TiO2 was easy to be resolved in the tungsten bronze phase. The microstructure of the composite ceramics were consisted of two kinds of grains. The smaller polygonal grains were belonged to the BST phase, and the larger ones to the SBN phase. The coexistence of the two phases inhibited the growth of the BST crystal. The density of microstructure of the composite ceramic was higher than that of both the pure BST and SBN calcined at the same temperature for the same time.展开更多
基金Project (11KJB430007) supported by the University Natural Science Research Program of Jiangsu Province, ChinaProject supported by the Priority Academic Program Development of Jiangsu Higher Education Institutions, China
文摘The dielectric properties and phase transition characteristics of La2O3- and Sb2O3-doped barium strontium titanate ceramics prepared by solid state route were investigated. The microstructure was identified by X-ray diffraction method and scanning electron microscope was also employed to observe the surface morphologies. It is found that （La,Sb）-codoped barium strontium titanate ceramics exhibit typical perovskite structure and the average grain size decreases dramatically with increasing the content of Sb2O3. Both La3＋ ions and Sb3＋ ions occupy the A-sites in perovskite lattice. The dielectric constant and dielectric loss of barium strontium titanate based ceramics are obviously influenced by La2O3 as well as Sb2O3 addition content. The tetragonal-cubic phase transition of La2O3 modified barium strontium titanate ceramics is of second order and the Curie temperature shifts to lower value with increasing the La2O3 doping content. The phase transition of （La,Sb）-codoped barium strontium titanate ceramics diffuses and the deviation from Curie-Weiss law becomes more obvious with the increase in Sb2O3 concentration. The temperature corresponding to the dielectric constant maximum of （La,Sb）-codoped barium strontium titanate ceramics decreases with increasing the Sb2O3 content, which is attributed to the replacement of host ions by the Sb3＋ ions.
基金Project(BK20140517)supported by the Natural Science Foundation of Jiangsu Province,ChinaProject(14KJB430011)supported by Jiangsu Provincial Natural Science Foundation for Colleges and Universities,China
文摘The microstructures and dielectric properties of Sb2O3-doped Ti deficient barium strontium titanate ceramics prepared by solid state method were investigated with non-stoichiometric level and Sb2O3content by SEM,XRD and LCR measure system.It is found that with the increase ofδ,(Ba0.75Sr0.25)Ti1-δO3-2δceramics transform from single phase solid solutions with typical cubic perovskite structure to multiphase compounds while(Ba0.75Sr0.25)Ti0.998O2.996ceramics remain to be single-phase with the increasing Sb2O3content.The distortion of the ABO3perovskite lattice caused by VTi″″and VO..induces the drop of Curie temperature and the rise of relative dielectric constant in(Ba0.75Sr0.25)Ti1-δO3-2δceramics with increasingδvalue.The orientation of VO??elastic dipoles results in the domain-wall pinning and thus the reduction of the dielectric loss.With increasing Sb2O3content,the relative dielectric constant,dielectric constant maximum and Curie temperature of(Ba0.75Sr0.25)Ti0.998O2.996ceramics decrease dramatically while the dielectric loss increases.
基金supported by National Natural Science Foundation of China(51767010)Science&Technology Key Research Project of Jiangxi Provincial Education Department(GJJ170760).
文摘A glass with composition of B_(2)O_(3)-Bi_(2)O_(3)-SiO_(2)-CaO-BaO-Al_(2)O_(3)-ZrO_(2)(BBSZ)modified Ba_(x)Sr_(1-x)TiO_(3)(BST,x=0.3 and 0.4)ceramics were prepared by a conventional solid state reaction method abided by a formula of BST+y%BBSZ(y=0,2,4,7,and 10,in mass).The effect of BBSZ glass content on the structure,dielectric properties and energy storage characteristics of the ceramics was investigated.The dielectric constant reduced but the endurable electrical strength enhanced due to the BBSZ glass addition in BST ceramics.In particular,the dielectric loss of the ceramics at elevated temperature(e.g.200℃)can be strongly suppressed from tanδ>20%to tanδ<3% after BBSZ glass modification.For Ba_(0.3)Sr_(0.7)TiO_(3)+2%BBSZ ceramics,an optimized energy storage density(γ=0.63 J/cm^(3))and efficiency(η=91.6%)under an applied electric field of 160 kV/cm was obtained at room temperature.Meanwhile,the temperature dependent polarization-electric field(P-E)hysteresis loops were measured to evaluate the energy storage characteristics of the ceramics potential for high voltage capacitor application at elevated temperatures.
文摘The influence of the composition （Yb2O3, MgO, CeO2, Li2CO3） on the dielectric properties of medium temperature sintering （Ba, Sr）TiO3 （BST） series capacitor ceramics was investigated by means of conventional technology process and orthogonal design experiments. The major secondary influencing factors and the influencing tendency of various factor＇s levels for the dielectric properties of BST ceramics were obtained. The optimum formula for maximum dielectric constant （ε） and for minimum dielectric loss （tanδ） was obtained under the experimental conditions. The BST ceramics with optimum comprehensive properties was obtained by means of orthogonal design experiments, with the sintering temperature at 1200 ℃, the dielectric constant 5239, the dielectric loss 0.0097, withstand electric voltage over 6 MV·m^-1, capacitance temperature changing ence of various components on the providing the basis for preparation rate （△C/C） - 75.67%, and suited for Y5V character. The mechanism of the infludielectric properties of medium temperature sintering BST ceramics was studied, thus of multilayer capacitor ceramics and single-chip capacitor ceramics.
文摘The effect of Yb2O3 doping amount on the dielectric properties of (Ba, Sr)TiO3 (BST) series capacitor ceramics prepared using solid state reaction method were studied. With the increasing of Yb2O3 doping amount, the dielectric constant(ε) of materials increased, the dielectric loss(tanδ) of materials decreased to minimum when w(Yb2O3) was 0.9%. The BST ceramics with high ε(10000), low tanδ(0.0213) and high DC breakdown voltage(7.2 kV·mm-1) were obtained. The influence of Yb2O3 doping amount on the structure of BST ceramics was studied by means of X-ray diffraction(XRD) and scanning electron microscope. The influencing mechanism of Yb2O3 on the dielectric properties of BST ceramics was studied. The results showed that Yb2O3 doping influenced the properties and structure of BST ceramics by means of forming defect solid solution, but did not influence crystal grain size,the crystal phase was single perovskite structure, did not influence XRD data of BST and did not improve capacitance temperature property greatly, but increase dielectric constant greatly. These results provided the basis for Yb2O3-doped BST series capacitor ceramics.
文摘In order to explore new application opportunities of Barium Strontium Titanate (BST) ceramic composite by modifying the conventional ferroelectric properties of BST through La<sub>2</sub>O<sub>3</sub> doping in BST matrix sintered at different temperature was investigated in this current study. Unadulterated Ba<sub>0.3</sub>Sr<sub>0.7</sub>TiO<sub>3</sub> (BST) matrix was prepared from BaTiO<sub>3</sub> (99.95%) and SrTiO<sub>3</sub> (99.95%) taken in stoichiometric extents which later doped by La<sub>2</sub>O<sub>3</sub> (99.99%) in varying extents (0.05 g, 0.10 g and 0.15 g) exploiting solid state reaction route. Doping caused drag effect for the penetration of impurities and sintering temperature helped the impurities migration to BST. Dielectric constant gets lower with rising of frequency, as electrons do not get enough time to polarize at high frequency. Dielectric constant and conductance are found maximum for the sample (0.1 g La<sub>2</sub>O<sub>3</sub> doped BST) sintered at 1460<span style="white-space:nowrap;">°</span>C and reverse is found in impedance analysis. These electrical properties showed visible frequency dependent response irrespective of sintering temperature and doping.
文摘Composite ceramics of 0.7BaO·0.3SrO·(1-y)TiO2·yNb2O5 (BSTN) with coexistence of barium strontium titanate, Ba1-xSrxTiO3 (BST), and strontium barium niobate, SrxBa1-xNb2O6 (SBN) phases were successfully prepared in situ by controlling excess components according to a specially designed formula of 0.7BaO·0.3SrO·(1-y)TiO2·yNb2O5 and by using a traditional ceramic process. X-ray diffractometry (XRD), scanning electron microscopy (SEM) and energy dispersion spectrometer (EDS) were used to characterize the phase composition, morphology and the micro-area chemical composition of the composite ceramics. The results showed that the SBN tungsten bronze phase appeared and coexisted stably with the BST perovskite phase when the excess content of Nb2O5 was >6mol%, whereas the BST perovskite phase formed and coexisted stably with the SBN tungsten bronze phase when the excess content of TiO2 was >5.3mol%. In the case of the two phases being equivalent to each other in BSTN composite ceramics, Nb2O5 was hard to be resolved into the perovskite phase, however, a few of TiO2 was easy to be resolved in the tungsten bronze phase. The microstructure of the composite ceramics were consisted of two kinds of grains. The smaller polygonal grains were belonged to the BST phase, and the larger ones to the SBN phase. The coexistence of the two phases inhibited the growth of the BST crystal. The density of microstructure of the composite ceramic was higher than that of both the pure BST and SBN calcined at the same temperature for the same time.
