成型压力对CrO2低温输运性质的影响

本文研究了压力对CrO2样品低温磁输运性质的影响.样品的X射线衍射结果表明(110)峰的相对强度随压力的增加而增大,说明压力对CrO2针状纳米颗粒有取向的作用.低温时CrO2样品的电阻和磁阻均随压力的增加而减少.实验结果表明,低温下样品的电导呈现出典型的晶粒间隧穿特征,其△值随着压力和磁场的增加而减小,并且△随磁场的变化幅度与成型压力有关,成型压力越高,△随磁场的变化越小.这些变化可以归因为压力对晶粒间隧穿势垒的调制.     

磁场下合成Fe3O4粉体的隧道磁阻

通过在半金属Fe₃O₄合成过程中外加磁场的方法,改变样品粒子的表面结晶状态和晶格缺陷,研究了由此引起的Fe₃O₄输运性质的变化.合成的Fe₃O₄粉体的主要导电机理均为自旋极化隧穿和高阶跃迁电导,电阻随温度升高成指数降低,电阻与电压显示了非线形相关性,磁阻与磁场的关系为蝴蝶形,是典型的隧道磁阻特征.与没有外加磁场时合成的样品比较,外加磁场合成的样品显示了更低的电阻和更高的磁阻. 关键词： 磁阻 隧穿 表面 晶格缺陷     

高压下TiO2纳米线晶粒和晶界性质及电输运行为

采用水热合成法制备了锐钛矿相TiO₂纳米线,并通过原位高压阻抗谱测量技术研究了TiO₂纳米线晶粒和晶界性质及电输运行为随压力的变化关系.研究结果表明:在0—34.0 GPa压力区间,锐钛矿TiO₂纳米线的传导机制为电子电导.TiO₂纳米线晶粒和晶界电阻以及弛豫频率在8.2—11.2 GPa压力区间均出现了不连续变化行为,此压力区域对应着由锐钛矿相到斜锆石相的结构转变,并且相变从晶粒表面逐渐延伸到晶粒内部.晶粒激活能和晶界激活能均随压力的增加而减小,说明压力对样品电导率的贡献为正.在所测压力范围内,空间电荷势始终为正值,表明在空间电荷区阴离子缺陷更易形成,氧缺陷是TiO₂纳米线相变的主要诱因.     

双势垒磁性隧道结的磁电阻效应及其在自旋晶体管中的应用

利用磁控溅射方法沉积双势垒磁性隧道结多层膜, 其中Al-O势垒层由等离子体氧化1 nm厚的 金属铝膜方式制备，然后采用深紫外光曝光和Ar离子刻蚀技术、微加工制备出长短轴分别为 6和3 μm大小的椭圆形双势垒磁性隧道结（DBMTJ），并在室温和低温下对其自旋电子输运 特性进行了研究. DBMTJ的隧穿磁电阻(TMR)比值在室温和42 K分别达到27％和423％， 结电阻分别为136 kΩ·μm²和175 kΩ·μm²，并在实验中观 察到平行状 态下存在低电阻态及共振隧穿效应，反平行态下呈现高电阻态以及TMR随外加偏压或直流电 流的增加而发生振荡现象. 由此，设计了一种基于这种双势垒磁性隧道结隧穿特性的自旋晶 体管. 关键词： 双势垒磁性隧道结 隧穿磁电阻 共振隧穿效应 自旋晶体管     

纳米多晶La0.7Sr0.3MnO3－δ的输运性质和磁电阻效应研究

利用溶胶-凝胶法制备了纳米多晶La_0.7Sr_0.3MnO_3-δ(LSM)块体样品.详细研究了在不同烧结温度下的LSM样品电阻率随测量温度的变化关系和磁电阻效应.随着测量温度从室温降低,电阻率ρ都在250K附近存在最大值,低于该温度后,样品表现为金属导电特性,随后在50K左右存在一极小值.即随着温度从50K左右降低到4.2K,ρ反而逐渐升高,表现为绝缘体性的导电特性.研究表明,在低温下(<50K),ρ随温度降低而升高的现象与隧穿效应的理论模型(lnρ∝T^1/2)符合得很好,表明这种现象是由于传导电子在通过邻近LSM晶粒间表面/界面层时的隧道效应所致.而在50—250K的温度范围内,其电阻率与T²成正比,表现为LSM本征的金属导电特性.因此这种低温下电阻率的极小值现象来源于隧穿效应和LSM晶粒本征的金属导电特性的相互竞争.本文还详细研究了相应的隧道磁电阻效应. 关键词： 0.7Sr_0.3MnO_3-δ')" href="#">多晶La_0.7Sr_0.3MnO_3-δ 隧道效应 隧道磁电阻效应     

非晶态软磁薄膜Fe90-xCoxZr10的平面霍耳效应和磁阻效应

本文研究了非易态软磁薄膜Fe_90-xCo_xZr₁₀的平面霍耳电压及磁阻随磁场方向、成分和温度的变化规律。采用通常的六探针法进行了测量。结果表明平面霍耳电压和磁阻分别满足经验公式V_y=pM²Isin2θ和△ρ=cM²cos2θ;并给出了V_y表达式中的常数项p正比于ρ²。此外,样品Co₉₀Zr₁₀和样品Fe₇₀Co₂₀Zr₁₀晶化前后的V_y变化正好相反,即富钴成分的样品晶化后,V_y增加,而富铁成分的样品V_y下降。 关键词：     

Ag掺杂La-K-Mn-O非均匀多晶体系的电磁性质

用溶胶-凝胶方法制备了1/mAg₂O-La_0.833K_0.167MnO₃ (LKMO/Ag)系列样品，其中1/m代表Ag₂O和La_0.833K_0.167MnO₃(LKMO)的摩尔比，m=32，16，8，4和2. 研究了此系列样品的结构、磁性和输运特性. X射线衍射实验表明，LKMO/Ag是一个非均匀的系统，样品由磁性的钙钛矿相LKMO和金属Ag相组成. 由于Ag相的加入，在室温条件下，磁电阻效应明显增强. 在300 K, 0.5 T磁场下，m=4样品的磁电阻可以达到32%；5.5 T磁场下，其磁电阻可达64%. 而单纯的LKMO样品在相同条件下的磁电阻分别为10%和35%. 在低温下，加Ag样品的磁电阻效应反而减小，样品含Ag越多，磁电阻效应越小. 用非本征磁电阻(包括自旋极化隧穿和自旋相关散射)和本征磁电阻在不同温区对总磁电阻的相对贡献对此系列样品的磁电阻现象作了定性的解释. 关键词： 自旋极化隧穿 自旋相关散射 低场磁电阻 高场磁电阻     

超薄栅氧化层n-MOSFET软击穿后的导电机制

研究了恒压应力下超薄栅氧化层n型金属-氧化物-半导体场效应晶体管（n-MOSFET）软击穿 后的导电机制.发现在一定的栅电压V_g范围内，软击穿后的栅电流I_g符合Fowl er-Nordheim隧穿公式，但室温下隧穿势垒_b的平均值仅为0936eV，远小于S i/Si O₂界面的势垒高度315eV.研究表明，软击穿后，处于Si/SiO₂界 面量子化能级上的 电子不隧穿到氧化层的导带，而是隧穿到氧化层内的缺陷带上._b与缺陷带能 级和电 子所处的量子能级相关；高温下，激发态电子对隧穿电流贡献的增大导致_b逐 渐降低. 关键词： 软击穿 栅电流 类Fowler-Nordheim隧穿 超薄栅氧化层     

a-SiNx/nc-Si/a-SiNx双势垒结构中的电荷隧穿和存储效应

在等离子体增强化学气相沉积系统中利用大氢稀释逐层淀积技术制备nc-Si量子点阵列,用硅烷和氨气混合气体淀积氮化硅层,制备了a-SiN_x/nc-Si/a-SiN_x不对称双势垒结构,其中隧穿和控制a-SiN_x层的厚度分别为3和20 nm.利用电导-电压和电容-电压测量研究结构中的载流子隧穿和存储特性.在同一样品中观测到由于电荷隧穿引起的电导峰和由于电荷存储引起的电容回滞现象.研究结果表明,合理地选择隧穿层和控制栅层的厚度,就能够实现载流子发生共振隧穿进入到nc-Si量子点中,并被保存在nc-Si量子点中. 关键词： nc-Si量子点 电导峰 存储效应     

K2NiF4型Sr2CrO4的磁电性质研究

以SrO和CrO₂为原料, 在高温高压的条件下直接反应生成纯相的K₂NiF₄结构的Sr₂CrO₄多晶样品. 结构用粉末X射线衍射及GSAS精修表征. 磁化率测试显示样品存在一个弱的反铁磁相变, 奈尔温度为T_N=95 K. 在奈尔温度以上, 磁化率随温度的变化遵循居里-外斯定律. 对样品进行了电阻测试, 结果显示了样品的绝缘特性.     

Improvement of the intergranular pinning energy in uniaxially compacting (Bi-Pb)<Subscript>2</Subscript>Sr<Subscript>2</Subscript>Ca<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>10+δ</Subscript> ceramic samples

Measurements of the electrical resistivity as a function of temperature, ρ(T), for different values of applied magnetic field, B_a (0 ≤ B_a ≤ 50 mT), were performed in polycrystalline samples of Bi_1.65Pb_0.35Sr₂Ca₂ Cu₃O_10+δ subjected to different uniaxial compacting pressure (UCP). We have found appreciable differences in the grain orientation between samples by using X-ray diffractometry. From the X-ray diffraction patterns performed, in powder and pellet samples, we have estimated the Lotgering factor along the (00l) direction, F_(00l). The results indicate that F_(00l) increases ~23% with increasing UCP suggesting that grains of these samples are preferentially aligned along the c-axis, which is parallel to the compacting direction. The resistive transition of the samples have been interpreted in terms of the thermally activated flux-creep model. In addition, the effective intergranular pinning energy, U₀, have been determined for different applied magnetic field. The magnetic field dependence of U₀, for B_a > 8 mT, was found to follow a H^{- α} dependence with α = 0.5 for all samples. The analysis of the experimental data strongly suggested that increasing UCP results in appreciable changes in both the grain alignment and the grain connectivity of the samples. We have successfully interpreted the data by considering the existence of three different superconducting levels within the samples: the superconducting grains, the weak-links, and the superconducting clusters.     

Magnetoresistance of porous polycrystalline HTSC: Effect of the transport current on magnetic flux compression in intergranular medium

The hysteretic dependences of the magnetoresistance of porous (38% of the theoretical density) granular high-temperature superconductor (HTSC) Bi_1.8Pb_0.3Sr_1.9Ca₂Cu₃O _x have been analyzed in the model of the effective intergranular field. This effective field has been defined by the superposition of the external field and the field induced by magnetic moments of superconducting grains. The magnetic flux compression in an intergranular medium, characterized by the effective field, controls the hysteretic behavior of the magnetoresistance. It has been found that the magnetoresistance hysteresis width for the studied porous HTSC depends on the transport current, in contrast to the superconductor of the same composition with high physical density (more than 90% of the theoretical value). For a porous superconductor, a significant current concentration occurs in the region of the grain boundaries, which is caused by features of its microstructure. A current-induced increase in the effective boundary length results in a decrease in the flux compression, a decrease in the effective field in the intergranular medium, and a magnetoresistance hysteresis narrowing with increasing current.     

Pressure effect on magnetic and insulator–metal transition of La0.67Pb0.33Mn0.9Co0.1O2.97 ceramic

In our paper, we study the effect of hydrostatic pressure on the magnetic and insulator–metal transitions of La_0.67Pb_0.33Co_0.1Mn_0.9O_2.97 manganite. The insulator–metal transition does not coincide with the magnetic transition in this ceramic. The compound undergoes the paramagnetic–ferromagnetic phase transition at T _C=260 K and the insulator–metal transition at T _p=184?K at ambient pressure. We have found that both characteristic temperatures T _C and T _p increase with increasing hydrostatic pressure with Δ T _C/Δ p=11.2 K/GPa and Δ T _p/Δ p=20.1 K/GPa, respectively.     

First principles study of structural,magnetic and electronic properties of half-metallic CrO<Subscript>2</Subscript> under pressure

A first-principles tight-binding linear muffin tin orbital (TB-LMTO) method within the local-density approximation is used to calculate the total energy, lattice parameter, bulk modulus, magnetic moment, density of states and energy band structures of half-metallic CrO₂ at ambient as well as at high pressure. The magnetic and structural stabilities are determined from the total energy calculations. From the present study we predict a magnetic transition from ferromagnetic (FM) state to a non-magnetic (NM) state at 65 GPa, which is of second order in nature. We also observe from our calculations that CrO₂ is more stable in tetragonal phase (rutile-type) at ambient conditions and undergoes a transition to an orthorhombic structure (CaCl₂-type) at 9.6 GPa, which is in good agreement with the experimental results. We predict a second structural phase transition from CaCl₂- to fluorite-type structure at 89.6 GPa with a volume collapse of 7.3%, which is yet to be confirmed experimentally. Interestingly, CrO₂ shows half metallicity under ambient conditions. After the first structural phase transition from tetragonal to orthorhombic, half metallicity has been retained in CrO₂ and it vanishes at a pressure of 41.6 GPa. Ferromagnetism is quenched at a pressure of 65 GPa.     

Magnetoresistive effect in RCu<Subscript>3</Subscript>Mn<Subscript>4</Subscript>O<Subscript>12</Subscript> perovskite-like oxides

The electrical properties of and the magnetoresistive effect in RCu₃Mn₄O₁₂ (R=rare-earth ion or Th) are studied. In all compounds of this series, the magnetoresistive effect amounts to 20% at liquid nitrogen temperature in the presence of a field of 0.9 T. An increase in the magnetoresistance with decreasing temperature and a high sensitivity to weak magnetic fields at low temperatures point to the intergranular nature of the effect. The magnetoresistance shows a peak in the vicinity of the Curie temperature T_C. Based on the dependences of the magnetoresistance on an external magnetic field, it is assumed that the magnetoresistance peak near T_C is related to the charge carrier scattering by magnetic inhomogeneities as in substituted orthomanganites. We believe that the magnetoresistance value near the magnetic ordering temperature depends on the synthesis conditions and the effect of the intergranular spacer on the transport properties of these compounds.     

Magnetoresistance and magnetic properties of Fe3O4 nanoparticle compacts

In this paper,we report on the magnetic properties of Fe3O4 nanoparticles with different grain sizes under different pressures.In all the samples,the saturated magnetization Ms shows a linear decrease with increasing pressure.The thickness of the magnetic dead layer on the nanoparticle surface nuder different pressures was roughly estimated,which also increases with increasing pressure.The transport measurements of the nanoparticle Fe3O4 compacts show that the low-field magnetoresistance (MR) value is insensitive to the grain size in a wide temperature range;however,the high-field MR value is dependent on grain size,especially at low temperatures.These experimental results can be attributed to the different surface states of the nanoparticles.     

GREAT MAGNETIC ENTROPY CHANGE IN La(Fe, M)13 (M=Si, Al) WITH Co DOPING

Very large magnetic entropy change Δ S_M, which originates from a fully reversible second-order transition at Curie temperature T_C, has been discovered in compounds La(Fe, Si)₁₃, La(Fe, Al)₁₃ and those with Co doping. The maximum change ΔS_M\approx19 J·kg^-1·K^-1, achieved in LaFe_11.4Si_1.6 at 209K upon a 5T magnetic field change, exceeds that of Gd by more than a factor of 2. The T_C of the Co-doped compounds shifts to higher temperatures. ΔS_M still has a considerable large magnitude near room temperature. The phenomena of very large ΔS_M, convenience of adjustment of T_C, and also thesuperiority of low cost, strongly suggest that the compounds La(Fe, M)₁₃ (M=Si, Al) with Co doping are suitable candidates for magnetic refrigerants at high temperatures.     

Spontaneous and field-induced magnetic transitions in YBaCo2O5.5

A detailed study of magnetic properties of cobaltite YBaCo₂O_5.5 has been performed in high (up to 35 T) magnetic fields and under hydrostatic pressure up to 0.8 GPa. The temperatures of paramagnet-ferromagnet (PM-FM) and ferromagnet-antiferromagnet (FM-AF) phase transitions and their pressure derivatives have been determined. It has been revealed that in the compound with yttrium, in contrast to those with magnetic rare earth atoms, the AF-FM field-induced magnetic phase transition is accompanied by a considerable field hysteresis below 240 K, and the magnetic field of 35 T is not sufficient to complete this transition at low temperatures. The hysteresis value depends on the magnetic field sweep rate, which considered as an evidence of magnetic viscosity that is especially strong in the region of coexistence of the FM and AF phases. High values of susceptibility for the field-induced FM phase show that Co spin state in these compounds changes in strong magnetic field.     

Specific features of magnetic and transport properties of La1−x Mn1+x O3 manganites

The magnetic and transport properties of La_1?x Mn_1+x O₃ manganites with excess manganese are studied. It is shown that magnetic and charge ordering heavily depends on the superstoichiometric manganese content, magnetic field, and pressure. The magnetoresistive effect (MRE) is enhanced as the manganese concentration increases. In addition to the paramagnet-ferromagnet transition, the temperature dependences of the magnetization exhibit anomalies at low temperatures in samples with x=0.1–0.4. The magnetization decreases at T<45 K in fields H<0.2 kOe and increases as H changes from 0.2 to 10 kOe. An analysis shows that the features observed at low temperatures are most probably related to the transition from the ferromagnetic state to the canted spin structure in clusters of mixed-valence manganese ions. The temperature dependences of the magnetization and resistivity remain unchanged as the pressure increases. It is demonstrated that the Curie and metal-dielectric transition temperatures shift to higher values as the manganese concentration increases under pressure. The temperature of the MRE peak increases under pressure, while the MRE decreases.