Magnetic and transport properties of bilayered manganites La1.2Sr1.8Mn2-xGaxO7（x=0,0.08）

The magnetic and electrical properties of nonmagnetic Ga +3 ion substitution for Mn site are investigated in the bilayer manganite La 1.2 Sr 1.8 Mn 2 O 7.When the Mn is substituted by Ga,the ferromagnetic property obviously weakens,the magnetic transition temperature decreases and a spin-glass behaviour occurs at low temperature.Meanwhile,doping causes the resistivity to dramatically increase,the metal-insulator transition temperature to disappear,and a greater magneto-resistance effect to occur at low temperature.These effects result from the fact that Ga substitution dilutes the magnetic active Mn-O-Mn network and weakens the double exchange interaction,and further suppresses ferromagnetic ordering and metallic conduction.     

Co掺杂对钙钛矿锰氧化物La0.8Sr0.2MnO3磁性的影响

采用传统的高温固相反应法制备La0.8Sr0.2Mn1-xCoxO3（x=0,0.1）系列多晶样品,采用X射线衍射（XRD）测量样品的结构,并用物性测量系统（PPMS）探究样品的磁化强度随温度的变化曲线（M-T）,以及在不同的温度下磁化强度随外加磁场的变化曲线（M-H）。结果表明：当温度高于TG时,样品呈现出纯顺磁态,当TG相似文献   

钙钛矿型锰氧化物(La_(0.8)Eu_(0.2))_(4/3)Sr_(5/3)Mn_2O_7的磁性和电性研究

采用传统固相反应法制备钙钛矿型锰氧化物(La0.8Eu0.2)4/3Sr5/3Mn2O7多晶样品,X-射线衍射分析表明,样品(La0.8Eu0.2)4/3Sr5/3Mn2O7结构呈现良好的单相.通过磁化强度随温度的变化曲线(M-T)、不同温度下磁化强度随磁场的变化曲线(M-H)和电子自旋共振谱发现:在300 K以下,随着温度的降低,样品先后经历了二维短程铁磁有序转变(T2D C≈282K)、三维长程铁磁有序转变(T3D C≈259K)、奈尔转变(T N≈208K)和电荷有序转变(T CO≈35K);样品(La0.8Eu0.2)4/3Sr5/3Mn2O7在T N以下,主要处于反铁磁态;在T3D C达到370 K时,样品处于铁磁-顺磁共存态,在370 K以上时样品进入顺磁态.此外,分析电阻率随温度的变化曲线(ρ-T)得到:样品在金属-绝缘转变温度(T P≈80K)附近出现最大磁电阻值,其位置远离T3D C,表现出非本征磁电阻现象,其磁电阻值约为61%.在T CO以下,电阻率出现明显增长,这是由于温度下降使原本在高温部分巡游的e g电子开始自发局域化增强所致.通过对(La0.8Eu0.2)4/3Sr5/3Mn2O7的ρ-T曲线拟合,发现样品在高温部分的导电方式基本遵循小极化子的导电方式.     

镝掺杂钙钛矿锰氧化物Gd0.67Ca0.33MnO3的磁性和磁卡效应EI北大核心CSCD

借助传统的固相反应法制备了多晶系列样品Gd0.67-xDyxCa0.33Mn O3(x=0,0.05,0.15),探究了Dy掺杂后对该系列样品磁性和磁卡效应的影响。研究结果表明：该系列样品呈现良好的单相性,均是立方钙钛矿结构,空间群为Pbnm;3个样品的铁磁性减弱、反铁磁性增强,并且Dy掺杂后系统内长程铁磁有序增强,形成了AFM团簇;通过该系列样品的临界行为分析,表明该系列样品均与平均场模型拟合较好;通过Arrott曲线和重标定曲线,发现母相和掺杂样品x=0.05,0.15均经历了一级相变到二级相变的过渡阶段;3个样品外加磁场为5 T的最大磁熵变值分别为1.53,1.44,1.40 J·kg-1·K-1。     

钙钛矿锰氧化物(La_(1-x)Gd_x)_(0.5)Sr_(0.5)MnO_3的磁电阻效应

采用传统的高温固相法制备了多晶样品(La1-xGdx)0.5Sr0.5MnO3(x=0,0.1,0.2,0.3,0.4),利用X射线衍射仪(XRD)、超导量子磁强计(SQUID)、标准四端引线法分别对样品结构、磁性、电性以及磁电阻效应进行了研究。研究表明:Gd的少量替代并没有引起结构变化;随着Gd含量的增加,所有样品的居里温度TC和金属-绝缘体转变温度Tp都降低了;在TC附近发现了磁电阻效应,同时在低温下发现了更大的磁电阻;并且Gd的少量替代可使磁电阻MR增大。     

Magnetic and transport properties of Dy substituted layered perovskite La1.3Sr1.7Mn2O7

The effect of Dy substitution for La site in layered manganese oxides La1.3-x Dyx Sr1.7 Mn2O7 on the magnetic and electrical properties has been investigated.With the La 3+ substituting by Dy3+,the long range three-dimensional ferromagnetism transition and the insulator-metal transition disappear.These effects are attributed to the lattice distortion due to the substitution of the smaller Dy3+.Addtionally,the small Dy3+ is inclined to occupy the R site which is in the rock-salt layer,then the distribution of La,Sr,Dy ions in Dy-doped sample should be more orderly than that in La1.3 Sr1.7 Mn2O7,so there is only one insulator-metal transition in the ρ-T curve of the sample with x = 0.05 and x = 0.1.     

Spontaneous magnetization and resistivity jumps in bilayered manganite （La0.8Eu0.2）4/3Sr5/3Mn2O7 single crystals

Owing to the inhomogeneous state resulting from the doping of a small number of Eu ions into Laa/3Sr5/3Mn2O7, from the resulting single crystal （La0.8Eu0.2）a/3Sr5/3Mn2O7 we have observed the magnetization jump, the resistivity jump, as well as the relaxation phenomena. For （Lao.sEuo.2）a/3Sr5/3Mn2O7, it has a very delicate ground state due to the interplays among spin, charge, orbital, lattice degrees of freedom. Consequently, the magnetization state is sensitive to temperature, magnetic field, as well as time. Meanwhile, the evolution of the magnetization with time shows a spontaneous jump when both the temperature and the magnetic field are constant. Similar step-like behaviours are also observed in resistivity. All these results suggest that Eu doping can greatly modulate the physical properties of Laa/3Sr5/3Mn2O7 and cause such interesting behaviours.     

Electron spin resonance study of the Ba-doping manganite Nd0.5Sr0.5MnO3

We have performed magnetization measurements and electron spin resonance （ESR） on polycrystalline manganites of Nd0.5Sr0.5-xBaxMnO3 （x = 0.1）. Phase separation and phase transitions are observed from the susceptibility and the ESR spectra data. Between 260 K （～ Tc） and 185 K （～ TN）, the system coexists of the paramagnetic phase and the ferromagnetic （FM） phase. Between 185 K and 140 K, the system coexists of the FM phase and the antiferromagnetic （AFM） phase. These results indicate that the system has a very complex magnetic state due to the origin of the instability stemming from manganite Nd0.5Sr0.4Ba0.1MnO3 by partially substituting the larger Ba^2＋ ions for the smaller Sr^2＋ ions.     

Eu 掺杂双钙钛矿氧化物 Dy2CoMnO6 的磁性研究

本文通过传统的固相反应方法制备了双钙钛矿氧化物系列样品 Dy2 -xEuxCoMnO6 (x =0,0.1 ,0.3) . 利用对该系列样品的 XRD 谱线、 磁化强度随温度的变化曲线(M-T ) 、 等温磁化曲线(M-H ) 的测量, 研究了随着Eu 掺杂对类 Griffiths 相、 磁熵变等的影响. 研究表明, 双层钙钛矿氧化物 Dy2 -xEuxCoMnO6 (x =0,0.1 ,0.3) 系列样品均显示出良好的单相性; 样品在T >TG 和T 相似文献   

钙钛矿型锰氧化物(La$lt;sub$gt;0.8$lt;/sub$gt;Eu$lt;sub$gt;0.2$lt;/sub$gt;)$lt;sub$gt;4/3$lt;/sub$gt;Sr$lt;sub$gt;5/3$lt;/sub$gt;Mn$lt;sub$gt;2$lt;/sub$gt;O$lt;sub$gt;7$lt;/sub$gt;的磁性和电性研究

采用传统固相反应法制备钙钛矿型锰氧化物 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇多晶样品, X-射线衍射分析表明, 样品(La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇结构呈现良好的单相. 通过磁化强度随温度的变化曲线(M-T)、不同温度下磁化强度随磁场的变化曲线(M-H)和电子自旋共振谱发现: 在300 K以下, 随着温度的降低, 样品先后经历了二维短程铁磁有序转变 (T_C^2D ≈ 282 K)、三维长程铁磁有序转变(T_C^3D ≈ 259 K)、奈尔转变(T_N ≈ 208K)和电荷有序转变(T_CO ≈ 35 K); 样品 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇在T_N以下, 主要处于反铁磁态; 在T_C^3D达到370 K时, 样品处于铁磁-顺磁共存态, 在370 K以上时样品进入顺磁态. 此外, 分析电阻率随温度的变化曲线(ρ-T)得到: 样品在金属-绝缘转变温度(T_P ≈ 80 K)附近出现最大磁电阻值, 其位置远离T_C^3D, 表现出非本征磁电阻现象, 其磁电阻值约为61%. 在T_CO以下, 电阻率出现明显增长, 这是由于温度下降使原本在高温部分巡游的e_g电子开始自发局域化增强所致. 通过对 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇的ρ-T 曲线拟合, 发现样品在高温部分的导电方式基本遵循小极化子的导电方式. 关键词： 磁性 电性 金属-绝缘转变温度 电子自旋共振