High Temperature LFMR in Yttrium Doped Perovskite Manganites

Porous ceramic samples of Y doped perovskite manganites were prepared. In these samples, the transition from high temperature paramagnetic insulator to low temperature ferromagnetic metal as well as the low field magnetoresistance (LFMR) effect at the low temperature is similar to that in dense samples. Opposite to that in dense samples, LFMR effect in porous sample is observed at the high temperature close to the peak of MR T curves. The results suggest that the high temperature LFMR effect and the applicable colossal magnetoresistance (CMR) materials could be obtained by controlling the microstructures of this class of perovskite manganites.

Behavior of Mn^(2+) in perovskite manganites with nominal composition La_(0.6-x)Nd_xSr_(0.1)MnO_3

The fact that there are Mn^(2+) at the A sites in the ABO_3 perovskite phase of manganites with the nominal composition La_(0.6-x)Nd_xSr_(0.1)MnO_3 showed by detailed experimental study and theoretical calculations.The magnetic moments of these Mn^(2+) are antiparallel to those of the Mn ions at the B sites.The content of the Mn^(2+) increases as the average ionic radius,<r_A>,of the ions at A sites decreases,resulting in the experimentally observed phenomenon that the content of the Mn_3O_4 phase in the manganites decreases with decreasing <r_A>.

Structural and magnetic properties of La_(0.7)Sr_(0.1)Ag_xMnO_(3-δ) perovskite manganites

Ag-doped manganite powder samples, La0.7Sr0.1AgxMnO3 6 （x = 0.00, 0.025, 0.05, 0.075, and 0.10） were synthesized using the sol-gel method. X-ray diffraction patterns indicated that the samples had two phases with the R-3c perovskite being the dominant phase and Mn3O4 being the second phase. X-ray energy dispersive spectra indicated that the ratio of Ag to La was very close to that of the nominal composition in the samples. The specific saturation magnetizations at 300 K increased from 32.0 A.mZ/kg when x = 0.00 to 46.8 A-mZ/kg when x = 0.10. The Curie temperature, TC, of the samples increased from 310 K when x = 0.00 to 328 K when x = 0.10. Because the atomic concentration ratios of La, Sr, and Mn in the five samples were all the same and only the Ag concentration changed, the variations of the specific saturation magnetizations at 300 K and the Curie temperatures suggested that the Ag cations have been doped into the A sites of the perovskite phase in the samples.

Negative Magnetism in Perovskite Manganites Gd1-xSrxMnO3（0.1 ≤x≤0.3）

A series of Sr-substituted Gd1-xSrxMnO3（0.1 ≤x≤0.3） materials was prepared via a standard method involving solid-state reaction. Their crystal structure within the entire doping region was determined to be orthorhombic perovskite type. The magnetic properties of the perovskite Gd1-xSrxMnO3（0.1 ≤x≤0.3） were thoroughly investigated. It appears that Mn ions with high valence state can induce stronger magnetization, and negative magnetization is evident in the manganites with x=0.1 and x=0.2, suggesting that valence fluctuation plays an important role in such systems. The result of XPS analysis indicates that the valence state of Mn ions is 3.25 and there seems to be excess amounts of oxygen in the structure of Gd0.8Sr0.2MnO3＋δ. In addition, the results of magnetization measurements demonstrate that spin reversal occurs only when the applied field is less than 1.99× 10^5 A/m, which presumably could be due to the negative exchange interaction between Mn sub-lattice and Gd sites.

Influence of Photon Pump Fluence on Charge Carriers in FAPbI3 and Manganite Perovskites

FAPbI3 and FA(Mn:Pb)I3 perovskite films were prepared and evaluated through steady and transient absorption spectroscopy. According to the analysis using Elliot’s model, there were no considerable differences except for the absorption intensity between FAPbI3 and FA(Mn:Pb)I3 perovskite films: the value of the optical gap (Eg) and the position of exciton resonance (E0) were the same. The femtosecond transient absorption showed biexponential relaxation properties of the charge carriers, suggesting that biexcitons are more easily generated in FA(Mn:Pb)I3 than FAPbI3 perovskite. The generation of biexcitons in FA(Mn:Pb)I3 was also confirmed by the photon pump fluence dependence. Moreover, we were able to estimate the average number of absorbed photons directly from the photon pump power dependence without needing any further experimental measurements such as photoluminescence. Our findings may offer a new way of understanding photoinduced carrier dynamics in perovskite manganites.

Magnetic Field Controllable Photocurrent Properties in BiFe_(0.9)Ni_(0.1)O_(3)/La_(0.7)Sr_(0.3)MnO_(3) Laminate Thin Film

This paper reports a multifunctional magnetic-photoelectric laminate device based on the integration of spintronic material(La_(0.7)Sr_(0.3)MnO_(3))and multiferroic(Ni-doped BiFeO_(3)),in which the repeatable modulation effect on the photoelectric properties were achieved by applying external magnetic fields.More obviously,photocurrent density(J)of the laminate was largely enhanced,the change rate of J up to 287.6%is obtained.This sensing function effect should be attributed to the low-field magnetoresistance effect in perovskite manganite and the scattering of spin photoelectron in multiferroic material.The laminate perfectly combines the functions of sensor and controller,which can not only reflect the intensity of environmental magnetic field,but also modulate the photoelectric conversion performance.This work provides an alternative and facile way to realize multi-degree-of-freedom control for photoelectric conversion performances and lastly miniaturize multifunction device.

Roles of Te and Mn in the two phases of manganite with nominal composition La_(0.6)Sr_(0.1)Te_xMnO_3

Powder samples with nominal composition La0.6Sr0.1TexMnO3 （x = 0.00, 0.05, 0.10, 0.15, 0.20） were prepared using the sol-gel method with thermal treatment up to 1473 K. On the basis of powder X-ray diffraction （XRD）, thermogravimetric and magnetic measurements, it was found that almost all of the Te and a few of the Mn ions were lost from the samples when they were calcined at 1473 K. The reason for the Te loss and a quantitative phase analysis for the samples calcined at 1473 K are discussed in detail.

Focused-Ion-Beam Induced Paramagnetic Defects in FAMn:PbI3 Perovskite Films

FAMn:PbI3 perovskite films were synthesized and probed mainly through electron spin resonance (ESR) spectroscopy. FAMn:PbI3 with low (~1%) Mn concentration showed a hyperfine sextet line originated from Mn++ ions. FAMn:PbI3 with high (10%) Mn concentration showed broad resonance (~500 G peak-to-peak linewidth). However, after bombardment of FAMn:PbI3 with high Mn concentration by focused ion beams (FIB), a sharp ESR peak appeared. The peak-to-peak linewidth (ΔHpp) was ~8 G regardless of the temperature. The FIB-induced defect showed Curie behavior at low temperatures (5 K - 50 K), which indicates the presence of localized electrons at the defect sites at low temperatures. The g-value increased from g = 2.0002 to 2.0016 as the temperature increased from 5 K to 50 K. Together with the ongoing search for electron spin echo (ESE), this could potentially provide a platform for realizing magnetic bits, information storage, and increased manipulation speed.

Transport-magnetism Correlation and Colossal Magnetoresistance in Mixed-valent Manganites

A phenomenological model based on phase separation between ferromagnetic metallic and paramagnetic insulating domains was applied to analyze the electrical transport and colossal magnetoresistance for mixed-valent manganites of RE_(2/3)AE_(1/3)MnO_3. The results show that the model can yield results in agreement with experimental observations in these manganites. The present approach provides a simple picture to visualize the reason that the temperature dependence of resistance (with and without applied magnetic fields) in these compounds has the peculiar shape, without invoking any complicated concept.

Enhancement of room-temperature magnetoresistance in La_(0.5)Sm_(0.2)Sr_(0.3)MnO_3/(Ag_2O)_(x/2)

La0.5Sm0.2Sr0.3MnO3/（Ag2O）x/2 （x = 0.00, 0.04, 0.08, 0.25, 0.30） samples were prepared by the solid-state reaction method, and their transport behaviors, transport mechanism, and magnetoresistance effect were studied through the measurement and fitting of p-T curves. The results show that the element Ag takes part in reaction when the doping amount is small. Ag is mainly distributed at the grain boundary of the host material and is in metallic state when the doping amount is relatively large; then the system becomes a two-phase composite. A small amount of Ag doping can apparently increase grain-boundary magnetoresistance induced by the spin-dependent scattering. The resistivity of the sample doped with 30 mol% Ag is one order of magnitude smaller than that of low-doped samples, and its magnetoresistance in the magnetic field of 0.5 T and at 300 K is strengthened apparently reaching 9.4%, which is connected not only with the improvement of the grain-boundary structure of the host material but also with the decrease of material resistivity.

Magnetoresistance enhancement and temperature stability of magnetoresistance in La_(1-x)(Sr_(1-y)Na_y)_xMnO_3

A series of the samples La_(1-x)(Sr_(1-y)Na_y)_xMnO_3(y=0.0,0.2,0.4,0.6,0.8,1.0) were prepared by the solid-state reaction method.Magnetoresistance enhancement and temperature stability of magnetoresistance in the system La_(1-x)(Sr_(1-y)Na_y)_xMnO_3 with unchanged Mn^(3+)/Mn^(4+) ratio through the doping of both monovalent and divalent elements at A site were studied through the measurements of X-ray diffraction(XRD) patterns,resistivity-temperature(ρ-T) curves and magnetoresistance-temperature(MR-T) curves.The results indicate that with the increase of Na doping amount,the peak value of MR increases,and it increases from 12.4% for y=0.2 to 50.6% for y=1.0 in the magnetic field B=0.8 T;ρ-T curves exhibit the double-peak phenomenon,which comes from the competition between the resistivity of surface phase and that of body phase;for the sample of y=0.8,MR increases slowly from 8.3% to 9.4% in the temperature range from 259 to 179 K,and MR is so stable in such a wide temperature range,which provides reference for the research on the temperature stability of MR.

Influence of the substitution of Sm, Gd, and Dy for La in La_(0.7)Sr_(0.3)MnO_3 on its magnetic and electric properties and strengthening effect on room-temperature CMR

A series of La0.7-xSmxSr0.3MnO3, La0.7-xGdxSr0.3MnO3, and La0.7-xDyxSr0.3MnO3 （x=0.00, 0.10, 0.20, 0.30） samples were prepared by the solid-state reaction method. The influence of the substitution of Sm, Gd, and Dy for La on the magnetic and electric properties and on the magnetoresistance （MR） was studied through measurements of M-T curves and p-T curves. The results showed that： lattice distortion induced by substitution of Sm, Gd, and Dy for La and extra magnetism of substitution had great influence on the magnetic and electric properties of pcrovskite manganites; substitution of magnetic rare earth element for La was an effective way to change Curie temperature and to strengthen MR in perovskite manganites; and appropriate substitution proportion would generate large MR near room temperature.

Destruction of charge ordering phase in La_(0.4)Ca_(0.6)MnO_3 induced by low Cr doping

Polycrystalline samples of La0.4Cao.6Mn1-xCrxO3 （x = 0.00, 0.02, 0.04, 0.06） were prepared by the solid state reaction method. The influence of Cr3＋ substitution for Mn3＋ on the magnetic property and charge ordering phase of La0.4Ca0.6MnO3 was studied through the measurements of X-ray diffraction （XRD）, magnetization-temperature （M-T） curves and electron spin resonance （ESR） spectra. The experimental results indicate that the mother＇s body of La0.4Ca0.6MnO3 has very complicated magnetic structure, exhibits charge ordering phase at 258 K, and shows long-range strongly correlated charge ordering-antiferromagnetism （CO-AFM） phase from 175 to 50 K. Spin glass state appears when the temperature decreases to about 41 K. When the Cr substitution amount is x = 0.06, the charge ordering phase of the mother＇s body is de-stroyed, because the Cr3＋ substitution for Mn3＋ destroys the spin order of CE-type antiferromagnetism, and thus leads to the melting of charge ordering. It is verified experimentally that the strong coupling between charge order and spin order exists in the charge order system of CE-type antiferromagnetism.

Low-field magnetoresistance of (1-x)La_(0.6)Dy_(0.1)Sr_(0.3)MnO_3/0.5x (Sb_2O_3) composite system under different sintering temperatures of matrix

A series of (1-x)La0.6Dy0.1Sr0.3MnO3/0.5x(Sb2O3)(x=0.15) samples were prepared by the solid-state reaction method, and the influence of sintering temperature of the matrix on low-field magnetoresistance of (1-x)La0.6Dy0.1Sr0.3MnO3/0.5x (Sb2O3) was studied through the measurements of X-ray diffraction (XRD) patterns, scanning electron microscope (SEM) image, resistivity-temperature (ρ-T) curves, and magnetoresistance-temperature (MR-T) curves. The results indicate that for the samples with low sintering temperature of the matrix, lowfield magnetoresistance effect appears on the whole temperature range and can be explained by grain boundary effect; for the sample with high sintering temperature of the matrix, intrinsic magnetoresistance peak appears on the high-temperature range, low-field magnetore-sistance effect appears on low temperature range, and the magnetoresistance in the magnetic field of 0.2 T and on the comparatively large temperature range between 280 K and 225 K hardly changes with temperature and remains at 4.8%, which can be explained by the competition between the intrinsic magnetoresistance induced by double-exchange function inside grains and the tunneling magnetoresis-tance (TMR) induced by grain boundary effect. The temperature stability of magnetoresistance is beneficial to the practical applications of MR.

Electric transport properties and temperature stability of magnetoresistance of composite system between La_(8/9)Sr_(1/45)Na_(4/45)MnO_3 and Sb_2O_3

The samples ofLa8/9Sr1/45Na4/45MnO3 （LSNMO）/x/2（Sb2O3） were prepared by the solid-state reaction method. The electric transport properties and the temperature stabil-ity of magnetoresistance （MR） of the samples were studied through the measurements of X-ray diffraction patterns, resistivity-temperature （ρ-T） curves, mass magnetization-temperature （σ-T） curves, and magnetoresistance-temper-ature （MR-T） curves. The results indicate that the p-Tcurves of the original material LSNMO show two peaks, and the phenomenon of two peaks of ρ-T curves disappears for the composite samples, which can be explained by a competition between surface-phase resistivity induced by boundary-dependent scattering and body-phase resistivity induced by paramagnetism-ferromagnetism transition. For all the sam-ples in the low temperature range, MR increases continu-ously with the decrease of temperature, which shows a characteristic of low-field magnetoresistance. However, MR basically keeps the same in the high temperature range. The paramagnetism-ferromagnetism transition is observed in the high temperature range due to a composite between perov-skite manganite and insulator, which can enhance the tem-perature of MR appearance in the high temperature range and make it to appear near room temperature. For the sample with x = 0.12, MR remains constant at the value of 7.5 % in the temperature range of 300-260 K, which achieves a tem-perature stability of MR near room temperature. In addition,for the sample with x = 0.16, MR is above 6.8 % in the high temperature range of 318-252 K （△T = 66 K）. MR almost remains constant in this temperature range, which favors the practical application of MR.

Electric and magnetic behaviour in double doped La2/3＋4x/3Sr1/3-4x/3Mn1-xMgxO3

The double-doped La2/3＋4x/3Sr1/3-4x/3Mn1-xMgxO3 samples with fixed Mn^3＋/Mn^4＋ ratio equal to 2/1 are investigated by means of magnetism and transport measurements. Phase separation is observed at temperature higher than T^onset c for x = 0.10 and 0.15. For x = 0.10, rather strong phase separation induces drastic magnetic random potential and results in the localization of carriers. Thus, the varlable-range hopping process dominates. For other samples, there is no or only weak phase separation above T^onset c. Thus, thermal activation mechanism is responsible for the high temperature transport behaviour. For x = 0.20 and 0.25, unexpected AFM behaviour is observed at low temperature. All these results are well understood by considering the special role of the ＂double-doping＂.

Enhancement of room-temperature magnetoresistance in La_(0.6)Dy_(0.1)Sr_(0.3)MnO_3/Ag_x

The samples of La0.6Dy0.1Sr0.3MnO3/（Ag2O）x/2（x = 0.00, 0.02, 0.04, 0.06, 0.08, 0.10, 0.20, 0.25, and 0.30） were prepared by using the solid-state reaction method.Their magnetic property, transport behavior, transport mechanism and magnetoresistance effect were studied through the measurements of magnetization-temperature（M-T） curves, ρ-T curves and the fitting of ρ-T curves.The results indicated that Ag could take part in the reaction when the doping amount is small.However, when the doping amount is comparatively large, Ag as metallic state mainly deposits on the grain boundary of La0.6Dy0.1Sr0.3MnO3, and then the system forms a two-phase composite.When the Ag doping amount is 30% mole ratio, the resistivity of the sample is one order of magnitude smaller than that of low doped samples, and its peak of magnetoresistance at 292 K and in the magnetic field of 0.2 T strengthens apparently and reaches 16.3%, which is over 7 times as large as 2.2% of La0.6Dy0.1Sr0.3MnO3.The two-phase composite system of magnetoresistance based on perovskite manganite consists of two parts：intrinsic magnetoresistance and extrinsic magnetoresistance.However, extrinsic magnetoresistance comes from spin-dependent scattering（SDS） and spin-polarized tunneling（SPT）.Magnetoresistance near TC increases due to the contribution of intrinsic magnetoresistance and extrinsic magnetoresistance formed by SDS, and magnetoresistance at low temperature is extrinsic magnetoresistance formed by SPT.

Infrared Spectra of La_(0.65)Ba_xMnO_(3-δ) Oxides

The infrared spectra of La_(0.65)Ba_xMnO_(3-|?￡(c) (x = 0.35, 0.33 and 0.30) were investigated experimentally. The result shows that the sample La_(0.65)Ba_xMnO_(3-|?￡(c) has the largest Curie temperature and the smallest resistivity and wave number of the stretching vibration mode of MnO_6 octaheUron at 300 K among the investigated samples. However, the absorption strength for the stretching vibration mode of Mn0_6 octahedron in La_(0.65)Ba_xMnO_(3-|?￡(c) is stronger for parainagnetic phase than that for ferromagnelic phase, which may be connected with the reducing of the dynamic in- coherent Jahn-Teller distortion below Curie temperature. In addition, the large shift of wave number for the stretching mode at the temperatures from 293 to 423 K has been observed in La_(0.65)Ba_xMnO_(3-|?￡(c), which may be due to the in- crease of the Mn-O bond length with temperature increasing.

Temperature stability of magnetoresistance (MR) and MR enhancement in La_(1-x)(Sr_(1-y)Ag_y)_x MnO_3 system

Polycrystalline samples of Lal-x（Srl-yAgy）x MnO3 （y = 0.0, 0.2, 0.4, 0.6, 1.0） were prepared by the solid-state reaction method. The temperature stability of magnetoresistance and magnetoresistance enhancement in Lal_x（Srl_yAgy）~MnO3 system with both univalent and bivalent elements doped at A site and with unchanged value of Mn~＋/Mn4＋ ratio were explored through the measurements of X-ray diffraction patterns, magnetiza- tion-temperature （M-T） curves, resistivity-temperature （p-T） curves and magnetoresistance-temperature （MR-T） curves. The results are as follows： there are two peaks in the p-T curves of the samples with Ag doping, one is caused by resistance change during the paramagnetism- ferromagnetism transition, and the other is from boundary- dependent scattering of conduction electrons on the boundaries of grains. The peak value of MR increases with increasing Ag doping content, and it increases from 8.2 % for y ---- 0.2 to 29.6 % for y ---- 1.0 under the magnetic field of B = 0.8 T; MR remains a constant of 12 % in the temperature range of 218-168 K for the sample with y = 1.0, and the temperature stability of MR is in favor of the practical application of MR.

Electrical Transport and Giant Magnetoresistance in (1-x)La_(0.67)Ca_(0.33)MnO_3/xCuO Composites

Samples with nominal composition of （1 - x）La0.67Ca0.33MnO3 （LCMO）/xCuO （x = 0%, 2%, 4% and 20% ） were made using a special experimental method. The temperature dependence of the resistivity （ρ） of the composites was investigated in the temperature range of 10 - 300 K and different magnetic fields of H = 0, 0.1, 0.3, 0.5, 1.0 and 3.0 T. The results showed that CuO percentage x had important effects on metal-insulator transition temperature （Tp）, zero field peak resistivity （ρmax）, and magnetoresistance （MR） properties of the composites. Tp shifted sharply towards low temperature with the increase of x in the range of x ≤4%, but was almost independent of x at high level of CuO content. Composites with x = 4 % and 20 % exhibited similar electrical transmission behavior. Compared with pure LCMO, enhanced magnetoresistance could be clearly observed even in a quite low magnetic field of 0.3 T. For x =4% and 20% samples, the MR value at 0.3 T could reach as high as - 88% and - 90%, respectively. XRD and SEM analysis showed that the substantial enhancement of MR, especially near Tp, was because of local spin disorder between contiguous LCMO ferromagnetic particles caused by the addition of CuO.