氧非正分La0.9Ba0.1MnO3-δ/SrTiO3:Nb p-n异质结的整流特性研究

利用脉冲激光沉积技术在掺Nb的SrTiO3衬底上制备了氧非正分La0.9Ba0.1MnO3-δ/SrTiO3:Nb p-n异质结.在20-300 K这一较宽的温度范围内获得了光滑的整流曲线.整流实验表明:该p-n异质结的正向扩散电压V0随着温度升高在薄膜金属-绝缘转变温度附近出现极大值,表现出与氧正分La0.9Ba0.1MnO3-δ/SrTiO3:Nb p-n结截然不同的温度特性.结合薄膜的电阻-温度实验和能带计算结果,对这一奇异的现象进行了解释.     

薄膜厚度对La0.67Ca0.33MnO3/Nb-SrTiO3异质结整流特性及磁阻的影响

利用脉冲激光沉积的方法,在Nb-1wt%:SrTiO3基片上分别生长了5 nm和50 nm的La0.67Ca0.33MnO3薄膜得到异质结.对该异质结电流-电压特性和磁阻的研究表明,50 nm厚的样品表现出良好的整流特性并且在外加1 T磁场的情况下无明显变化,而5nm厚的样品在低温下,整流特性发生变化,并且外加1 T磁场对其整流特性有明显影响,显示负的磁阻.通过考虑p～n结耗尽层的厚度,对观察到的实验现象进行了解释.     

La1.3Sr1.7Mn2O7/SrTiO3-Nb异质结的整流和光伏特性

采用脉冲激光沉积法在SrTiO₃:0.7%Nb(100)单晶衬底上生长了La_1.3Sr_1.7Mn₂O₇(LSMO)薄膜, 并 研究了LSMO/SrTiO₃-Nb异质结的输运性质和光伏效应. 研究发现, 异质结具有良好的整流特征和明显的光生伏特效应. 在532 nm激光辐照下, 光生电压随温度升高先增大后减小, 并且在150 K达到最大值400 mV, 此温度点与LSMO薄膜发生金属-绝缘体转变的温度一致, 这表明异质结的光生伏特效应受LSMO薄膜内部的输运特征调控. 进一步, 从光生电压随时间的变化曲线中分析发现, 上升沿符合一阶指数函数, 这与载流子的迁移过程相关; 而下降沿符合二阶指数函数, 这与结两侧载流子的外部回路中和以及材料内部的电子-空穴湮灭有关. 值得注意的是, 上升沿和下降沿的时间常数均随着温度先增大后减小, 且最大值均出现在LSMO薄膜的金属-绝缘转变温度.     

YBa2Cu3O7－δ/SrNb0.01Ti0.99O3 p-n结的制备及其特性

采用脉冲激光沉积技术，在n型SrNb001Ti099O3(SNTO)单晶基片上生长p型YBa2Cu3O7-δ(YBCO)薄膜，制备出YBCO/SNTO p n结.YBCO薄膜是高度c轴织构的超导薄膜，且具有良好的超导电性.YBCO/SNTO p n结具有较好的整流特性和很好的温度与磁场稳定性. 关键词： YBa2Cu3O7-δ SrNb001Ti099O3 p n结     

氧非正分La0.9Ba0.1MnO3-δ/SrTiO3:Nb p-n异质结的整流特性研究

利用脉冲激光沉积技术在掺Nb的SrTiO₃衬底上制备了氧非正分La_0.9Ba_0.1MnO_3-δ/SrTiO₃:Nb p-n异质结.在20—300K这一较宽的温度范围内获得了光滑的整流曲线.整流实验表明：该p-n异质结的正向扩散电压V_D随着温度升高在薄膜金属—绝缘转变温度附近出现极大值,表现出与氧正分La_0.9Ba_{0. 关键词： 0.9}Ba_0.1MnO_3-δ薄膜')" href="#">La_0.9Ba_0.1MnO_3-δ薄膜 锰氧化物p-n结 整流性质     

包含超巨磁电阻材料的p-n结

最近,来自美国北卡罗莱纳州立大学的TiwariA等制成了一种由p型锰氧化合物La0 .7Sr0 .3 MnO3 (LSMO)和n型ZnO层构成的p -n结.这种异质结构在2 0—30 0K的宽温区内具有整流功能.高质量异质结构的研制是自旋电子学中的一个重要领域.Ti wari等的工作为各具独特性能的两种材料的集成     

La2/3Sr1/3MnO3/BaTiO3复合薄膜的制备及其电致磁电效应研究

使用脉冲激光沉积技术,在LaAlO₃(001)单晶基片上制备了La_2/3Sr_1/3MnO₃(LSMO)/BaTiO₃(BTO)双层薄膜.X射线衍射分析显示,LSMO层和BTO层呈现纯(001)取向.原子力显微镜研究表明,薄膜表面晶粒大小均匀,排列致密,表面均方根粗糙度为1.4 nm.复合薄膜的磁学、电学性能研究表明,其具有良好的磁学和介电性能.电输运测试显示,与在BTO层上施加正方向 关键词： 磁电效应 铁电/铁磁异质结构 脉冲激光沉积     

Pr0.5Ca0.5MnO3/Si异质结输运特性和整流特性研究

利用固相反应法制备Pr_0.5Ca_0.5MnO₃(PCMO)靶材,并采用脉冲激光沉积法(PLD)在n型Si(111)基片上沉积PCMO外延薄膜,研究了薄膜的输运特性及薄膜与Si衬底形成异质结的整流特性.结果表明:在80—300 K温度范围内,PCMO薄膜的阻温关系符合变程跳跃模型,随着温度的升高表现出从一维到二维再到三维的转变,分析认为可能源于轨道自由度对电子输运特性的影响.PCMO/Si异质结在磁场作用下整流特性得到改善,且在正向电流方向出 关键词： 0.5Ca_0.5MnO₃')" href="#">Pr_0.5Ca_0.5MnO₃ Si 整流 正磁电阻     

BaTiO3/p-Si异质结的整流特性和光诱导特性的研究

利用脉冲激光沉积法成功制备了BaTiO₃/p-Si异质结, 该异质结在80–300 K 显示出了良好的整流特性和光诱导特性. 开启电压随着温度的升高而逐渐降低. 利用不同频率的光子辐照样品, 观察到明显的光电导效应. 且随着照射光子能量的增大, 结电流也相应变大, 光诱导效应越明显. BaTiO₃薄膜电阻-温度(R-T) 曲线显示氧缺陷条件下BaTiO₃薄膜具有良好的半导体特性. 关键词： 异质结 光诱导效应 3薄膜')" href="#">BaTiO₃薄膜     

(La0.7Sr0.3MnO3)m(BiFeO3)n超晶格间隔的La0.7Sr0.3MnO3三明治结构制备及表征

采用射频磁控溅射的方法在SrTiO3(001,基片上制备了(La0.7Sr0.3MnO3)m(BiFeO3)n超晶格间隔的La0.7Sr0.3MnO3三明治结构.X射线衍射分析证明(La0.7Sr0.3MnO3)m(BiFeO3)n具有明显的超晶格结构.电流垂直于薄膜表面测得的电阻-温度关系表明.La0.7Sr0.3MnO3)m(BiFeO3)n超晶格薄膜在290 K有金属-绝缘体转变,略低于单层La0.7Sr0.3MnO3薄膜的转变温度.电流在0.01-10 mA范围内,观察到薄膜的峰值电阻随电流增大而减小,峰值变化率远大于单层La0.7Sr0.3MnO3薄膜,且随着超晶格周期厚度的增加而增大.低温下,电流-电压曲线表明其导电机制应主要为空间载子限制,且显示较大的电压偏置,表现出肖特基结的特性.     

The ν3 and 2ν3 bands of SO3, SO3, SO3, and SO3

This sixth of a series of publications on the high-resolution rotation-vibration spectra of sulfur trioxide reports the results of a systematic study of the ν₃ and 2ν₃ infrared bands of the four symmetric top isotopomers ³²S¹⁶O₃, ³²S¹⁸O₃, ³⁴S¹⁶O₃, and ³⁴S¹⁸O₃. An internal coupling between the l=0(A₁^′) and l=2(E^′) levels of the 2ν₃ states was observed. This small perturbation results in a level crossing between |k−l|=9 and 12, in consequence of which the band origins of the A₁^′,l=0 “ghost” states could be determined to a high degree of accuracy. Ground and upper state rotational constants as well as vibrational anharmonicity constants are reported. The constants for the center-of-mass substituted species ³²S¹⁶O₃ and ³⁴S¹⁶O₃ vary only slightly, as do the constants for the ³²S¹⁸O₃, ³⁴S¹⁸O₃ pair. The S-O bond lengths for the vibrational ground states of the species ³²S¹⁶O₃, ³⁴S¹⁶O₃, ³²S¹⁸O₃, and ³⁴S¹⁸O₃ are, respectively, 141.981 99(1), 141.979 38(6), 141.972 78(8), and 141.969 93(8) pm, where the uncertainties, given in parentheses, are two standard deviations and refer to the last digits of the associated quantity.     

Optical conductivity of CePd3, YPd3 and PrPd3

The optical conductivity of intermediate valence CePd₃ at 300 K exhibits a maximum near 16 meV, which is absent in the reference materials YPd₃ and PrPd₃. Using a modified Drude model with a memory function ansatz this anomaly has been identified as a resonant electron-electron scattering process of conduction electrons at the localized 4f states near the Fermi level E_F. The model fit gives estimates of the width of the 4f states, of their separation from E_F and of the f-d hybridization energy. Intra-4f transitions of CePd₃ are stronger compared to those of PrPd₃ due to the stronger f-d hybirdization. 4d→4f transition energies of CePd₃ are reduced due to an electron-hole Coulomb binding energy.     

The first-principles study of ferroelectric behaviours of PbTiO3/SrTiO3 and BaTiOn/SrTiO3 superlattices

We have performed the first-principles calculation to investigate the origins of ferroelectricities and different po- larization behaviours of superlattices BaTiO3/SrTiO3 and PbTiO3/SrTiO3. The density of state （DOS） and electronic charge profiles show that there are strong hybridizations between atoms Ti and O and between atoms Pb and O which play very important roles in producing the ferroelectricities of superlattices BaTiO3/SrTiO3 and PbTiO3/SrTiO3. Ow- ing to the decline of internal electric field in SrTiO3 （ST） layer, the tetragonality and polarizations of superlattices decrease with increasing the fraction of SrTiO3 in the superlattices. We find that the polarization of PbTiO3/SrTiO3 is largerthan that of BaTiO3/SrTiO3 at the same ratio of components, because the polarization mismatch between PbTiO3 and SrTiO3 is larger than that between BaTiO3 and SrTiO3. The polarization and tetragonality are en- hanced with respect to those of bulk tetragonal BaTiO3 in the superlattices BaTiO3/SrTiO3, while the polarization and tetragonality are reduced with respect to those of bulk tetragonal PbTiO3 in superlattices PbTiO3/SrTiO3.     

Li2K(IO3)3与Li2NH4(IO3)3的晶体结构

本文用X射线粉末法测定了Li₂K(IO₃)₃与Li₂NH₄(IO₃)₃的晶体结构和原子参数。发现Li₃K(IO₃)₃,Li₂NH₄(IO₃)₃与Li₂Rb(IO₃)₃同晶型,属单斜晶系,空间群为P2₁/α,每个单胞含有四个化合式量。室温的点阵常数分别为α=11.198?,b=11.046?,c=8.254?,β=111.53°,及α=11.327?,b=11.078?,c=8.341?,β=111.87°。讨论了二元化合物的形成与离子半径的关系。 关键词：     

Low temperature far IR spectra of (CH34)N NiCl3, (CH3)4N NiBr3 and (CD3)4N NiBr3

The known phase transition in (CH₃)₄N NiCl₃, at 171 K, has been characterised by far IR spectroscopy. The transition is explained as due to a formation of weak labile C-H,…, Cl hydrogen bonds at low temperatures, restricting the “free” internal rotations of the methyl groups and perhaps at the same time ordering the orientations of the tetramethylammonium ions. No similar transition in (CH₃)₄N NiBr₃ was found.     

Structure,electrical and magnetic properties of CaAs3, SrAs3, BaAs3 and EuAs3

The crystal structures and electrical properties of CaAs₃, SrAs₃, BaAs₃ and EuAs₃ have been studied by single crystal X-ray investigations, temperature dependent resistivity measurements and optical measurements. The structures of the triclinic CaAs₃ and monoclinic SrAs₃, BaAs₃ and EuAs₃ are closely related. The two-dimensional infinite polyanionic AS₃^2? nets are derivatives of the black phosphorus structure. CaAs₃ and BaAs₃ are semiconducting, while SrAs₃ and EuAs₃ show semimetallic behavior. The paramagnetic EuAs₃ undergoes a magnetic phase transition at 10.5 K.     

Heats of solution/substitution in TlNO3 and CsNO3 crystals and in RbNO3 and CsNO3 crystals from heats of transition: the complete phase diagrams of TlNO3-CsNO3 and RbNO3-CsNO3 systems

From measurements of the decrease in the heat (enthalpy) of transition in the solid phase using differential scanning calorimetry, the apparent molar heats of solution, slope ΔH_t/x, the partial molar heats of solution at infinite dilution, χ, and the heats of solution, ΔH_s^°, of Tl⁺ in CsNO₃ crystal and Cs⁺ in TlNO₃ crystal and Rb⁺ in CsNO₃ crystal and Cs⁺ in RbNO₃ crystal along with their recovered lattice energies, ΔH_L^°, are reported. ΔH_s^° of Tl⁺ and Rb⁺ in CsNO₃ crystal are each found to be negligible or zero representing an ideal solid solution, i.e. ΔH_mix=0. The complete phase diagrams of the TlNO₃-CsNO₃ and RbNO₃-CsNO₃ systems with details of the sub-solidus regions are included. The properties of Tl_(1−x)Cs_xNO₃ and Rb_(1−x)Cs_xNO₃ compositions are discussed in terms of a ‘mixed crystal’ or ‘crystalline solid solution’ in relation to parallel compositions of Tl_(1−x)Rb_xNO₃.     

Far ultraviolet reflectance spectra of CeF3, PrF3 and NdF3

Near-normal incidence reflectance measurements are carried out on thin films of CeF₃, PrF₃ and NdF₃ in the energy range of 6–40 eV. Tentative interpretations are given for different observed structures.     

Ionic conductivity of the perovskites NaMgF3, KMgF3, KMgK3 and KZnF3 at high temperatures

We have carried out a study of the ionic conductivity of NaMgF₃, KMgF₃ and KZnF₃ up to temperatures close to the melting point. Our results, in contrast to previous reports in the literature, show no abnormal ionic conductivity at high temperatures. Care in interpretation of results is required because of surface electronic conduction.     

Microwave spectrum of (CH3)3CCN-SO3

Eight rotational transitions of the complex (CH₃)₃CCN-SO₃ have been recorded using pulsed-nozzle Fourier transform microwave spectroscopy and a series of ab initio calculations has been performed. The complex is a symmetric top with free or nearly free internal rotation of the SO₃ and (CH₃)₃CCN subunits. The nitrogen-sulfur bond distance is determined to be 2.394(19) Å. Calculations at the MP2/aug-cc-pVTZ level/basis, which are in excellent agreement with the experimental results, give a binding energy of 11.0 kcal/mol relative to (CH₃)₃CCN and SO₃. Physical properties of the system, including N-S bond length, N-S-O angle, binding energy, and the degree of electron transfer (obtained from Townes and Dailey analysis of the ¹⁴N nuclear quadrupole coupling constant) are compared with those of similar complexes. The proton affinity of the base is a useful parameter for ordering complexes in the series.