La0.33Pr0.34Ca0.33MnO3薄膜的应变效应

采用脉冲激光沉积法分别在(100)LaAlO3和(100)SrTiO3基片上生长了La0.33Pr0.34Ca0.33MnO3 薄膜,并通过磁测量和电输运测量对生长在不同基片上的La0.33Pr0.34Ca0.33MnO3薄膜的物性进行了研究.结果表明,基片和薄膜之间的压应力导致La0.33Pr0.34Ca0.33MnO3薄膜容易出现铁磁相,而电荷有序相则被抑制.基片和薄膜之间的张应力则导致La0.33Pr0.34Ca0.33MnO3薄膜容易出现电荷有序相,铁磁相被抑制.导致该现象的可能原因之一是应力使得晶格中Mn-O键角发生改变而引起双交换作用的改变.     

La0.7Ca0.3MnO3超大磁电阻材料正电子湮没研究

对La0.7Ca0.3MnO3材料样品在77K至室温范围的一系列温度, 测量了正电子寿命谱和多普勒展宽谱.结果表明在居里温度附近正电子平均寿命和多普勒线形参数S出现明显变化, 反映了此类化合物晶格结构的不稳定性.本文对此进行了讨论.     

La0.67Ca0.33MnO3薄膜中的各向异性应变与电荷有序

本文采用脉冲激光沉积法在NdGaO3(001)单晶衬底上制备了一系列的La0.67Ca0.33MnO3薄膜,实验主要研究了薄膜的输运性质.La0.67Ca0.33sMnO3块材是铁磁金属基态,而La0.67Ca0.33MnO3/NdGaO3(001)薄膜由于各向异性应变的存在,可以观测到电荷有序绝缘相的出现.薄膜样品表...     

La0.67Ca0.33MnO3薄膜皮秒光电效应

在1064 nm波长脉冲激光（脉宽25 ps）的照射下，钙钛矿氧化物薄膜La0.67Ca0.33MnO3/SrTiO3具有超快光电效应，对激光脉冲显示ps量级的响应时间，上升沿响应时间300 ps，半高宽700 ps，同时，对激光能量的响应灵敏度为500 mV/mJ。     

Pr0.7Ca0.3MnO3陶瓷晶界势垒的交流特性

采用固相烧结方法制备了Pr1-xCaxMnO3(x=0.3)钙态矿结构锰氧化物陶瓷样品,对其在磁场和电场下的直、交流输运性质做了系统研究.通过测量加磁场和零场下的Ⅰ-Ⅴ曲线,得到其居里温度为150K,与VSM测试结果一致.通过测量加磁场与零场下交流的阻抗频谱,发现加磁场后样品的晶界电阻明显减小,而晶粒电阻几乎保持不变,表明Pr1-xCaxMnO3陶瓷多晶样品的CMR效应源于样品的晶界.为确定晶界处的势垒高度,测量了样品在不同频率下的阻抗温谱,根据Arrhenius定律拟合得出势垒高度为117 meV,与用直流R-T数据拟合得出的激活能一致.     

La0.67Ca0.33MnO3的磁特性研究

采用高温固态反应法制备了具有钙钛矿结构的锰氧化物La0.67Ca0.33MnO3,利用X射线衍射、超导量子干涉仪等实验技术研究其结构和磁性质。应用标度律对起依赖于磁场的始磁化强度在t→0时的行为用临界指数β随磁场变化进行描述。临界指数β随着磁场的增大而减小,说明在临界点附近,磁场的增大导致自旋有序度的增加。     

La0.7-xGdxSr0.3MnO3体系中的相分离

采用固相反应法制备了样品La0.7-xGdxSr0.3MnO3(x=0.00,0.20,0.30,0.40,0.50).通过测量样品的M～T曲线,ESR曲线,研究了La0.7-xGdxSrO0.3MnO3,体系中的相分离现象及相分离与CMR之间关系.结果表明:当x=0.30,0.40时,在PM-FM相变区产生相分离,并且磁电阻MR得到增强.研究结果表明:La0.7-xGdx Sr0.3MnO3中的相分离与Gd在A位的占位情况紧密相关,磁电阻MR的增强是在外磁场作用下,铁磁区扩大顺磁区减小引起的.     

Cr掺杂对Nd0.7Sr0.3MnO3电磁性质的影响

我们对多晶样品Nd0.7Sr0.3Mn1-xCrxO3(x≤0.30)进行了X射线衍射谱、电阻温度关系和磁化强度测量.实验发现:随Cr掺杂量的增加,样品的电阻率变大,电阻峰温度和居里温度降低,这是由Cr的介入弱化了双交换作用所致;在x=0.10附近,电阻出现了双峰现象,在其M~T上没有发现与低温峰对应的磁性异常;在锰位磁矩与Cr含量的关系中发现,Cr掺杂对样品的磁性几乎无贡献;通过分析,我们用相分离的图象解释了有关的现象.     

Mo低掺杂La0.67Sr0.33MnO3的磁电特性及室温磁电阻增强

采用固相反应法成功制备了Mo低掺杂La0.67Sr0.33Mn1-xMoxOc(x=0,0.02)单相多晶样品,系统研究了样品的磁性、电输运特性和磁电阻效应.发现Mo低掺杂对La0.67Sr0.33MnO3 的居里温度影响很小,但在La0.67Sr0.33MnO3铁磁基态背景下诱导出团簇自旋玻璃态行为.在低温区(0.1相似文献   

La0.67Ca0.33MnO3复合体系的磁电阻增强效应

在La0.67Ca0.33MnO3(LCMO)纳米颗粒体系中,采用Cu与之复合,考察复合对磁电阻性能的影响.结果表明,复合使低场磁电阻得到大幅度的增强.但和其它LCMO复合体系截然不同的是,复合体系的电阻率大幅下降.认为是在LCMO颗粒周围形成一层良导体,电子输运与颗粒边界的电子散射有关.     

Ti/Pr0.7Ca0.3MnO3/La0.67Sr0.33MnO3/Pt异质结电致电阻效应的改善

采用脉冲激光沉积技术制备了Ti/Pr_0.7Ca_0.3MnO₃/Pt和Ti/Pr_0.7Ca_0.3MnO₃/La_0.67Sr_0.33MnO₃/Pt异质结并研究了La_0.67Sr_0.33MnO₃功能插层对异质结电致电阻特性的影响. 实验结果表明La_0.67Sr_0.33MnO₃功能层的引入有效提高了器件的电阻转变特性,尤其是电阻转变率和疲劳性得到了极大的改善. 对La_0.67Sr_0.33MnO₃插层改善电致电阻转变特性的机理进行了定性的分析. 关键词： 电致电阻效应 电阻转变比率 疲劳特性     

Magnetotransport properties of La0.67Ca0.33MnO3//La0.67Sr0.33MnO3 bilayers

The perovskite bilayers La0.67Ca0.33MnO3 （LCMO） （100 nm） / La0.67Sr0.33MnO3（LSMO） （100 nm） and LSMO （100 nm） / LCMO （100 nm） are fabricated by a facing-target sputtering technique. Their transport and magnetic properties are investigated. It is found that the transport properties between them are different obviously due to distinguishable structures, and the different lattice strains in both films result in the difference of metal-to-insulator transition. Only single-step magnetization loop appears in our bilayers from 5K to 320K, and the coercive force of LSMO/LCMO varies irregularly with a minimum ～ 2387A/m which is lower than that of LCMO and LSMO single layer films. The behaviour is explained by some magnetic coupling.     

Influence of microstructures on exchange bias behaviors of La0.7Sr0.3MnO3/La0.33Ca0.67MnO3 bilayers

Ferromagnetic La_0.7Sr_0.3MnO₃ (LSMO) and antiferromagnetic La_0.33Ca_0.67MnO₃ (LCMO) layers were grown on SrTiO₃ (STO) substrates by the pulsed laser deposition technique. LSMO films had rougher surfaces and larger grain sizes than LCMO films. Fully strained bilayers, in which each layer was as thin as 10 nm, were prepared by changing their stacking sequences, i.e. LSMO/LCMO/STO and LCMO/LSMO/STO. The former had higher T_C (350 K) than the latter (300 K), and exchange bias effects were only observed in the former bilayers. This revealed that microstructures could play an important role in the transport and magnetic properties of manganese oxide thin films.     

Electrical and magnetic behavior of La0.7Ca0.3MnO3/La0.7Sr0.2Ca0.1MnO3 composites

The electrical transport properties and the magnetoresistance of La_0.7Ca_0.3MnO₃/La_0.7Sr_0.2Ca_0.1MnO₃ composites are investigated as a function of sintering temperature. On the basis of an analysis by X-ray powder diffraction and scanning electron microscopy we suggest that raising the sintering temperature enhanced the interfacial reaction and creates interfacial phases at the boundaries of the La_0.7Ca_0.3MnO₃ and La_0.7Sr_0.2Ca_0.1MnO₃. Results also show that in 3 kOe, and at the Curie temperature, the magnetoresistance value of 14% was observed for the composite sintered at 1300 °C. Based on the phenomenological equation for conductivity under a percolation approach, which depends on the phase segregation of ferromagnetic metallic clusters and paramagnetic insulating regions, we fitted the experimental resistivity—temperature data from 50-300 K and find that the activation barrier decreases as temperature is increased.     

Magnetocaloric effect in La0.67Sr0.33MnO3 manganite above room temperature

The La_0.67Sr_0.33MnO₃ composition prepared by sol-gel synthesis was studied by dc magnetization measurements. A large magnetocaloric effect was inferred over a wide range of temperature around the second-order paramagnetic-ferromagnetic transition. The change of magnetic entropy increases monotonically with increasing magnetic field and reaches the value of 5.15 J/kg K at 370 K for Δμ0H=5 T. The corresponding adiabatic temperature change is 3.3 K. The changes in magnetic entropy and the adiabatic temperature are also significant at moderate magnetic fields. The magnetic field induced change of the specific heat varies with temperature and has maximum variation near the paramagnetic-ferromagnetic transition. The obtained results show that La_0.67Sr_0.33MnO₃ could be considered as a potential candidate for magnetic refrigeration applications above room temperature.     

室温下Pr0.7Ca0.3MnO3薄膜的瞬态光响应特性

在室温下利用波长532nm，脉冲宽度7ns的纳秒脉冲激光研究了不同电压和激光能量密度作用下Pr_0.7Ca_0.3MnO₃薄膜的瞬态光响应特性.在激光能量密度为275.16mJ/cm²时，其最大电阻变化率达到92.3%，响应时间约36ns.室温下电压变化对薄膜的光响应特性影响不大，而诱导光能量密度的影响则很明显，能量密度越大，电阻变化越大，响应时间越短，并且电阻变化和响应时间均与激光能量密度呈非线性关系.这种光响应来源于薄膜中的光致非稳态绝缘体-金属相变，有望在新型光电器件上获得应用.     

Pico-second photoelectric characteristic in manganite oxide La0.67Ca0.33MnO3 films

Ultrafast photoelectric characteristic has been observed in La_0.67Ca_0.33MnO₃ films on tilted SrTiO₃ substrates. A pico-second (ps) open-circuit photovoltage of the perovskite manganese oxide films has been obtained when the films were irradiated by a 1.064μm laser pulse of 25 ps duration. The rise time and full width at half-maximum of the photovoltage pulse are ～300 ps and ～700 ps, respectively. The photovoltaic sensitivity was as large as ～500 mV/mJ.     

Response of the capacitance of a planar La0.67Ca0.33MnO3/SrTiO3/La0.67Ca0.33MnO3 heterostructure to an electric field

Manganite film electrodes were integrated with a spacer layer of strontium titanate to produce an epitaxial La_0.67Ca_0.33MnO₃/(1000 nm)SrTiO₃/La_0.67Ca_0.33MnO₃ (LCMO/STO/LCMO) heterostructure by laser ablation. At T = 300 K, the mechanical stresses in the STO layer relaxed to a considerable extent, while the LCMO electrodes were found to be under biaxial lateral tensile strain, with the lattice unit cell of the top electrode distorted considerably stronger (a _∥/a _⊥ ≈ 1.026) than that of the bottom electrode (≈1.008) (a _∥ and a _⊥ are the unit cell parameters in the substrate plane and along the normal to its surface, respectively). The reciprocal of the capacitance C of the plane-parallel LCMO/STO/LCMO film capacitors thus formed increased almost linearly with increasing temperature T in the range 50–250 K. At T < 100 K, the capacitance C decreased by approximately 50% in an electric field E = 40 kV/cm. After the electric field E was varied as 0 → + 100 kV/cm → 0, the capacitance C decreased by approximately 3% and the maximum in the C(E, T > 200 K) dependence shifted by approximately 9 kV/cm with respect to the point E = 0.     

Direct measurement of the magnetocaloric effect in La0.67Ca0.33MnO3

Polycrystalline perovskite La_0.67Ca_0.33MnO₃ was synthesized by a sol–gel method. Its adiabatic temperature change ΔT_ad induced by a magnetic field change was measured directly. At 268 K, near its Curie temperature T_C, ΔT_ad of La_0.67Ca_0.33MnO₃ induced by a magnetic field change of 2.02 T reaches 2.4 K. The latent heat Q and magnetic entropy change −ΔS_M induced by a magnetic field change were calculated from the temperature dependence of ΔT_ad and zero-field heat capacity C_p. The maximum values of Q and −ΔS_M in La_0.67Ca_0.33MnO₃ induced by a magnetic field change of 2.02 T are 1.85 J g⁻¹ and 6.9 J kg⁻¹ K⁻¹, respectively. The former is larger than the phase transition latent heat of heating or cooling, which is about 1.70 J g⁻¹.