Sr0.6Ba0.2Ca0.2Al2O4 ∶Eu,Dy的制备与长余辉发光性能研究

采用高温固相法制备了Ca,Ba共掺的Sr_0.6Ba_0.2Ca_0.2Al₂O₄ ∶Eu²⁺_0.01, Dy³⁺_0.02和单掺Ba的Sr_0.6Ba_0.4Al₂O₄ ∶Eu²⁺_0.01, 关键词： 长余辉 铝酸锶 稀土掺杂 陷阱能级     

Mn3Zn0.8Ni0.2N的高压同步辐射研究

 利用金刚石对顶压砧,对钙钛矿型金属锰化物Mn₃Zn_0.8Ni_0.2N进行了原位高压同步辐射角散X射线衍射研究。研究表明,在0~29.9 GPa的压力区间内,样品没有发生结构相变,因而在该压力下样品的物性变化并非由结构相变所导致。卸压以后,样品的特征峰都回到了初始位置。通过Birch-Murnaghan方程,拟合得到了样品的体弹模量为86.5 GPa。     

Ni0.8Co0.2-SiO2颗粒膜中的Hall效应

对用离子束溅射制备的Ni_0.8Co_0.2-SiO₂颗粒膜的Hall效应进行了研究.当Ni_0.8Co_0.2合金的含量为43vol%时,在9.5×10⁵A/m的外磁场下,样品的室温Hall电阻率达6.3μΩ·cm ,高于普通磁性金属两个数量级以上,还研究了不同NiCo组分样品的电阻率与温度的关系（95—300K）,发现x＜x_c(逾渗组分)时,电阻率与-logT成正比,电阻温度系数为负;当x＜x_c时,逐渐呈现金属性;而当x≈x_c时,为过渡态.还用透射电子显微镜和振动样品磁强计等手段对样品的微结构和磁性进行了对比研究,表明金属-绝缘体颗粒膜中在逾渗阈值附近有较大的Hall效应,这与样品的微结构有密切关系. 关键词：     

Chemical expansion of La0.8Sr0.2Fe0.7Ga0.3O3-δ

This paper deals with the chemical expansion measurements and modelling of La_0.8Sr_0.2Fe_0.7Ga_0.3O_3-δ. The expansion behavior has been evaluated using a dilatometer and X-ray diffraction over a wide range of temperatures (RT to 1373 K) and oxygen partial pressures (10^− 21 to 1 atm). The material stoichiometry evolution with temperature and oxygen partial pressure has been measured using thermogravimetry analysis at different oxygen partial pressure, from 10^− 21 to 0.5 atm and from RT to 1473 K. Considering a typical defect model for lanthanum ferrite oxides, chemical expansion depends linearly on the Fe⁴⁺ concentration rather than on the oxygen vacancy concentration. A model of chemical expansion as a function of pO₂ and temperature is then proposed. It helps to understand and anticipate the chemical expansion behavior exhibited by this material when used as Ionic Transport Membrane (ITM).     

Microstructure and electrode properties of La0.6Sr0.4Co0.2Fe0.8O3-δ spin-coated on Ce0.8Sm0.2O2?δ electrolyte

Fine and uniform La_0.6Sr_0.4Co_0.2Fe_0.8O_3−δ powder was synthesized by a glycine–nitrate combustion process. La_0.6Sr_0.4Co_0.2Fe_0.8O_3−δ electrodes were prepared on dense Ce_0.8Sm_0.2O_2−δ electrolyte substrates using a spin-coating technique by sintering at 900–1,000 °C. The electrode properties of La_0.6Sr_0.4Co_0.2Fe_0.8O_3−δ were investigated by electrochemical impedance spectroscopy and chronopotentiometry techniques with respect to preparation conditions and the resulting microstructures. The results indicate a significant effect of the microstructure on the electrode processes and polarization characteristics. The oxygen adsorption and dissociation process acted as a larger contribution to the overall electrode polarization R _p in magnitude compared with the charge transfer process due to relatively low porosity levels of the electrodes. It was detected that the grain size of the electrodes exhibited a crucial role on the electrocatalytic reactivity. At 800 °C, the electrode sintered at 950 °C attained a polarization resistance of 0.18 Ω cm², an overpotential of 27 mV at a current density of 200 mA cm⁻², and an exchange current density of 308 mA cm⁻².     

铁基超导体Li0.8Fe0.2ODFeSe的红外光谱研究

测量和研究了铁基超导体Li_0.8Fe_0.2ODFeSe单晶的红外光学响应,发现室温下光电导率谱不存在Drude分量,载流子具有非相干输运行为.随着温度降低,Drude分量形成并不断变窄,同时在相应的反射率谱上出现清晰的等离子体边,表明散射率急剧降低.在最低温度,观察到超导能隙形成导致的光谱变化,光电导率谱在160 cm^-1以下受到显著压制.对比FeSe单晶的光谱数据,发现整体的光电导率谱型很相似,但自由载流子的谱重更低,揭示出样品具有更低的载流子浓度.另外还观察到温度变化诱导的谱重由低频向高频区域转移的现象,表明其存在强关联效应.     

(La0.2Nd0.8)0.67Pb0.33MnO3的Preisach分析

测量了居里点为TC=220K的钙钛矿(La0.2Nd0.8)0.67Pb0.33MnO3 (LNPMO)在外场为ha=3978.87A/m ，2K相似文献   

Cyclic voltammetry characterization of a La0.8Sr0.2Co0.2Fe0.8O3 − δ electrode interfaced to CGO/YSZ

The electrochemical characteristics of a La_0.8Sr_0.2Co_0.2Fe_0.8O_3 − δ cathode electrode interfaced to the CGO layer of a double layer CGO/YSZ electrolyte were studied using cyclic voltammetry, at temperatures of 600 to 850 °C and under oxygen partial pressures ranging from 0.07 to 21 kPa. The aim was to identify the electrochemical processes taking place under cathodic polarization on the basis of differences in the features of the cyclic voltammograms with changing conditions. Depending on temperature, sweep rate and oxygen partial pressure, current peaks appeared both in the forward and backward scans. Furthermore, reversed hysteresis was observed, i.e. higher currents in the backward scan than in the forward scan, with increasing oxygen partial pressure and decreasing temperature. The observed behavior was related to the electrochemical redox of B-sites and concomitant stoichiometry change as well as to the competing reaction of electrochemical oxygen redox, taking also into account the competitive action of chemical reactions occurring in the presence of gaseous oxygen.     

晶粒尺寸对Bi0.2Ca0.8MnO3电荷有序的影响

利用溶胶-凝胶法制备了平均晶粒尺寸在38—1500 nm的系列Bi_0.2Ca_0.8MnO₃多晶样品,研究了它们的结构、电输运性质和磁性.研究结果表明,随着晶粒尺寸的减小,电荷有序逐渐消失、最后被完全压制,导致低温下出现自旋玻璃态.利用马氏体相变图像和表面效应解释了相关现象. 关键词： 钙钛矿锰氧化物 电荷有序 马氏体相变 自旋玻璃     

Crystallization and electrochemical performance of La0.6Sr0.4Co0.2Fe0.8O3 − δ-Ce0.8Gd0.2O1.9 thin film cathodes processed by single solution spray pyrolysis

La_0.6Sr_0.4Co_0.2Fe_0.8O_3 − δ-Ce_0.8Gd_0.2O_1.9 (LSCF-CGO) thin films obtained by spray pyrolysis of a single precursor solution were investigated by XRD, TEM and impedance spectroscopy at annealing temperatures ranging from 500 to 900 °C. Films annealed at 600 °C contained a mixture of amorphous regions and crystalline regions composed of fine crystallites (< 5 nm). Annealing above 600 °C increased the ratio of crystalline to amorphous material, led to the segregation of the films into distinct LSCF and CGO phases, and promoted grain growth. The electrical behavior of the films depended on annealing temperature. At testing temperatures of 400 °C and below, the polarization resistance of films with lower annealing temperatures was larger than the polarization resistance of films with higher annealing temperatures. However, at testing temperatures of 500 °C and above the polarization resistance of films with lower annealing temperatures was equal to or lower than the polarization resistance of films with higher annealing temperatures. This was reflected by the activation energy that decreased with increasing annealing temperature. The varying electrical behavior may be related to microstructural changes that caused bulk diffusion to be the rate-limiting step in films with lower annealing temperatures and oxygen dissociation to be the rate-limiting step in films with higher annealing temperatures.     

Mixed Conduction in BaCe0.8Pr0.2O3-α Ceramic

以高温固相反应法合成了BaCe0.8Pr0.2O3-α陶瓷,用X射线衍射法对其结构进行了表征. 用交流阻抗谱、气体浓差电池和氢泵方法测定了材料在500-900 ffiC、不同气氛中的电导率以及离子迁移数,研究了材料的导电特性. 结果表明,该陶瓷材料为单一钙钛矿型斜方晶结构. 在500-900ffiC下,在干燥和潮湿的氧气、空气和氮气气氛中,材料以电子空穴导电为主,其总电导率随氧分压的增加而稍有增加;在潮湿的氢气气氛中,材料以离子导电为主,其总电导率比不含氢气气氛(O2,air,N2)中的电导率高一到两个数量级.     

The magnetization reversal behaviour for SmCo6.8Zr0.2 and SmCo6.8Zr0.2/α-（Fe,Co） nanocrystalline magnets at low temperature

This paper reports that the SmCo 6.8 Zr 0.2 nanocrystalline permanent magnets and SmCo 6.8 Zr 0.2 /α-(Fe,Co) nanocomposite permanent magnets are successfully produced by mechanical alloying and subsequently annealing at 700 C for 10 minutes.The x-ray diffraction results show that the phase structure of SmCo 6.8 Zr 0.2 nanocrystalline permanent magnets is composed of SmCo 7 phase and SmCo 6.8 Zr 0.2 /α-(Fe,Co) nanocomposite permanent magnets is composed of SmCo 7 and α-(Fe,Co) phases.The mechanism of magnetization reversal is mainly controlled by inhomogeneous domain wall pinning in SmCo 6.8 Zr 0.2 and SmCo 6.8 Zr 0.2 /α-(Fe,Co) magnets.The inter-grain exchange interaction at low temperature is investigated,which shows that the inter-grain exchange interaction of SmCo 6.8 Zr 0.2 /α-(Fe,Co) magnets increases greatly by the decrease of the measured temperature.According to Δm irr-H/H cj,Δm rev-H/H cj and χ irr-H/H cj curves at room temperature and 100 K,the changes of irreversible and reversible magnetization behaviours of SmCo 6.8 Zr 0.2 and SmCo 6.8 Zr 0.2 /α-(Fe,Co) magnets with the decreasing temperature are analysed in detail.The magnetic viscosity and the activation volume of SmCo 6.8 Zr 0.2 and SmCo 6.8 Zr 0.2 /α-(Fe,Co) magnets at different temperatures are also studied.     

准静水冷压处理后的Bi0.8Pb0.2SrCaCu2Ox超导材料

着重讨论了准静水冷压对Bi系高温超导材料超导电性的影响,并分析了经冷压-退火处理后超导电性的改善情况。准静水冷压处理后,Bi系超导材料晶粒间界连接发生显著退化,晶粒内部产生大量缺陷,由此导致了宏观超导电性的退化。冷压造成了体密度的极大提高和一定的晶粒择优取向。这些现象主要是由于准静水压下剪切应力的作用。退火后,晶界连接得到很大加强,部分缺陷消失或形成堆错使材料各项性能均获改善。J_c(77K,零场)较初始样品有大幅度提高,达约1600A/cm²。此外还考察了静水压 关键词：     

(Ni0.8Zn0.2Fe2O4)epoxy-PZT双层膜中的磁电效应

讨论了Ni_0.8Zn_0.2Fe₂O₄ (NZFO)与锆钛酸铅(PZT)的双层膜结构样品的磁电(ME)效应.NZFO粉料由溶胶-凝胶法制成，再经900℃热压，并高温烧结.在该双层膜中测量到了很强的磁电相互作用.发现横向的磁电效应比纵向效应大一个数量级，并且随NZFO烧结温度的提高而增加.当烧结温度从950℃上升到1380℃时，横向ME电压系数(α_E)的最大值变化范围为25.6 mV Am^-2≤α_E≤199.6 mV Am^-2.理论分析显示NZFO-PZT双层膜样品中ME效应源于NZFO与PZT之间相对良好的磁电耦合. 关键词： 镍铁氧体 PZT 热压法 ME效应     

Hg0.9Tl0.2Ba2Ca2Cu3O8+δ在磁场下的热导

实验研究了高温超导体Hg09Tl02Ba2Ca2Cu3O8+δ的低温热导率与温度和磁场的关系,测量温度为7—20K,外加磁场为0—6T.结果表明,在不同外场下,超导体的热导率在实验温区内随温度的增加均单调增加;在固定的温度下外加磁场使超导体的热导率减小,并随外磁场的增加达到一个稳定值;热导的相对变化率κ(H)/κ(0)与磁场的关系以及热导率达到稳定值的磁场与测量温度有关.分析讨论了超导体中正常态电子在磁场下受磁通涡旋散射产生附加的热阻 关键词：     

Ba0.98Ce0.8Tm0.2O3-α的离子导电性及其燃料电池性能

用高温固相反应法制备了Ba_0.98Ce_0.8Tm_0.2O_3-α钙钛矿型氧化物固溶体,粉末X射线衍射表明该固溶体为单相. 用交流阻抗谱技术和气体浓差电池方法研究了样品在500～900 oC、不同气体气氛中的导电性,以及该样品为固体电解质的氢-空气燃料电池性能. 该电池能稳定地工作,在900 oC时,电池的最大功率密度为110.2 mW/cm²,高于以Ba_xCe_0.8RE_0.2O₃^- (x≤1, RE=Y, Eu, Ho)为固体电解质的氢-空气燃料电池的功率密度     

Bi0.8Ba0.2FeO3/La0.7Sr0.3MnO3异质结制备及其交换偏置效应研究

采用脉冲激光沉积方法, 通过调节激光能量、激光频率、衬底温度、氧压、靶基距等工艺参数, 在(100)取向的铝酸镧单晶衬底上制备出Bi_0.8Ba_0.2FeO₃/La_0.7Sr_0.3MnO₃多铁性异质结. X射线衍射图谱表明薄膜呈钙钛矿结构, 高分辨透射电镜图谱和能量色散X射线图谱表明两相界面清晰且具有良好的匹配度, 异质结呈(00l)取向性生长. 加场冷却条件下不同温度的磁滞回线(M-H)测量结果表明样品具有明显的交换偏置效应, 交换偏置场(H_EB)随温度的线性变化可能与异质结界面处电子轨道的重构和界面处自旋、轨道自由度之间的复杂的相互作用有关.     

Bi1.8Nd0.2Ti4O11的温致及压致软模相变研究

 采用背用散射的方法，测量了Bi_1.8Nd_0.2Ti₄O₁₁的拉曼光谱。实验结果表明，该掺杂样品发生温致和压致软模相变的温度和压力分别为200 ℃和3.35 GPa。文中讨论了相变点移动的原因及高频声子模随温度和压力的变化。     

CO2对Ba0.5Sr0.5Co0.8Fe0.2O3−δ表面氧交换的影响

采 用 了 一 种 新 的 脉 冲 同 位 素 交 换 技 术 , 研 究了CO₂对Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3?δ(BSCF)的表面氧交换动力学的毒害作用．当BSCF暴露于CO₂时,由于在材料表面形成了碳酸盐,其表面交换率严重降低．在低CO₂浓度(1%)时,毒害作用从375 oC开始,并且随着温度的上升而变得更加明显．同时,表面交换动力学的下降导致BSCF在CO₂条件下氧渗透性能快速下降．