Heusler合金Mn50–xCrxNi42Sn8的相变、磁性与交换偏置效应

研究了Mn50–xCrxNi42Sn8 (x=0, 0.4, 0.6, 0.8)多晶样品的相变、磁性和交换偏置效应.结果表明,该系列合金在室温下都具有非调制的四方马氏体结构.马氏体逆相变温度随Cr含量增加而逐渐降低. 20 k Oe磁场下的M-T曲线表明,该系列合金的磁性比较弱.两相之间的磁性差最大为△M=7.61 emu/g.磁性的变化主要与Mn-Mn间距的变化以及Ni(A位)-Mn(D位)间杂化作用的强弱有关.在低温下,马氏体相的磁性随着Cr含量增加而增强.在500 Oe的外加磁场作用下,从室温冷却到5 K,在Mn50Ni42Sn8合金中观察到高达2624 Oe的交换偏置场.随着Cr含量的增加,交换偏置场逐渐减小.当Cr含量x=0.8时,随着冷却场的增加, 5 K时的交换偏置场先迅速增加然后逐渐减小.当冷却场为500 Oe时,交换偏置场最大.这主要归因于自旋玻璃态与反铁磁性区域的界面交换耦合作用的变化.     

Influence of Ni/Mn ratio on magnetostructural transformation and magnetocaloric effect in Ni_(48-x)Co_2Mn_(38+x)Sn_(12)(x = 0, 1.0, 1.5, 2.0,and 2.5) ferromagnetic shape memory alloys

An investigation on the magnetostructural transformation and magnetocaloric properties of Ni_(48-x)Co_2Mn_(38+x)Sn_(12)(x = 0, 1.0, 1.5, 2.0, and 2.5) ferromagnetic shape memory alloys is carried out. With the partial replacement of Ni by Mn in the Ni_(48)Co_2Mn_(38)Sn_(12) alloy, the electron concentration decreases. As a result, the martensitic transformation temperature is decreased into the temperature window between the Curie-temperatures of austenite and martensite. Thus, the samples with x = 1.5 and 2.0 exhibit the magnetostructural transformation between the weak-magnetization martensite and ferromagnetic austenite at room temperature. The structural transformation can be induced not only by the temperature,but also by the magnetic field. Accompanied by the magnetic-field-induced magnetostructural transformation, a considerable magnetocaloric effect is observed. With the increase of x, the maximum entropy change decreases, but the effective magnetic cooling capacity increases.     

Correlation between reentrant spin glass behavior and the magnetic order-disorder transition of the martensite phase in Ni-Co-Mn-Sb Heusler alloys

We have performed ac susceptibility and dc magnetization measurements in Ni(50-x)Co(x)Mn(38)Sb(12) Heusler alloys. From the ac susceptibility measurements, the existence of reentrant spin glass (RSG) state is observed for x=0-5. It is found that the signature of RSG behavior diminishes with increase in x. This behavior is in contrast to the fact that the exchange bias field increases with x, which reveals that the origins of RSG and exchange bias are different in the present system. It is found that the system enters a frustrated ferromagnetic state just below the Curie temperature of the martensite phase (T(M)(C)) and then the RSG state at low temperature. The strength of the RSG state is critically dependent on the sharpness of the magnetic transition at (T(M)(C)). This proposition is further supported by the thermo-remanent magnetization and low field thermomagnetic measurements.     

Effects of Cu on the martensitic transformation and magnetic properties of Mn_(50)Ni_(40)In_(10) alloy

The structures, the martensitic transformations, and the magnetic properties are studied systematically in Mn50Ni40-xCuxIn10, Mn50-xCuxNi40In10, and Mn50Ni40In10-xCux alloys. The partial substitution of Ni by Cu reduces the martensitic transformation temperature, but has little influence on the Curie temperature of austenite. Comparatively, the martensitic transformation temperature increases and the Curie temperature of austenite decreases with the partial replacement of Mn or In by Cu. The magnetization difference between the austenite phase and the martensite phase reaches 70 emu/g in Mn50Ni39Cu1In10; a field-induced martensite-to-austenite transition is observed in this alloy.     

Effects of R-site compositions on the meta-magnetic behavior of Tb_(1-x)Pr_x(Fe_(0.4)Co_(0.6))_(1.88)C_(0.05)(x=0, 0.8, and 1)

We investigate the low-temperature magnetic properties of intermetallic compounds Tb1-xPrx(Fe0.4Co0.6)1.88C0.05(x = 0, 0.8, and 1) by detailed magnetization measurements. Obvious temperature- and field-induced irreversibilities suggest the coexistence of multiple magnetic phases. Sharp magnetization jumps across the antiferromagnetic to ferromagnetic transition are observed only in the Pr-containing samples, indicating that the behavior of the avalanche-like growth of ferromagnetic clusters is mainly related to the light lanthanide Pr ions. In addition, the time relaxation, field sweep rate, and cooling field dependence of magnetization jumps in the sample with x = 1 are consistent with those in the martensitic scenario.     

Strain glass behaviour of Ni–Co–Mn–Sn ferromagnetic shape memory alloys

We report the direct experimental observations of the glassy behaviour in Ni–Co–Mn–Sn ferromagnetic shape memory alloys by doping sufficient substitutional point defect Co into the Ni sites (9 at%). The results showed that high level of Co doping had caused the complete suppression of the martensitic transformation and introduction of a strain glass transition in Ni–Co–Mn–Sn alloys. The strain glass transition was definitively characterized by the dynamic mechanical anomalies following the Vogel–Fulcher relationship and the signature nonergodicity of the frozen glass using a zero‐field‐cooled/field‐cooled heating measurement of static strain. The findings clarified the cause of vanishing of the martensitic transformation in Ni–Co–Mn–Sn alloy with high Co doping levels and the generality of glassy state in Ni–Mn based ferromagnetic shape memory alloys with high level of foreign elements doping. (© 2015 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

The magnetic properties across the martensitic transition in the Co38Ni34Al28 alloy

The magnetic properties of the Co₃₈Ni₃₄Al₂₈ alloy have been studied. The alloy exhibits a first order austenite-martensite phase transition in the temperature region between 155 and 247 K. A strain of 0.07% is produced across this phase transition. The Arrott plots obtained from the isothermal magnetic field dependence of magnetization indicate the presence of spontaneous magnetization both in the austenite and martensite phases, confirming the ferromagnetic character of the alloy up to room temperature. The temperature dependence of the high field magnetization indicates the presence of spin wave excitations, spin wave excitation gap and spin wave-spin wave interactions in the martensite phase. The magnetic anisotropy energy constant for the Co₃₈Ni₃₄Al₂₈ alloy is estimated both with the help of the standard law of approach to saturation of magnetization, and also from the field dependence of magnetization using the field for technical saturation of magnetization. The temperature dependences of these energy terms are compared. The estimated values of the magnetic anisotropy constant seem to be in agreement with the magnitude of the spin wave excitation gap estimated from the temperature dependence of high field magnetization.     

Metastability and inverse magnetocaloric effect in doped manganite (Nd(0.25)Sm(0.25)Sr(0.5)MnO(3)) and ferromagnetic shape memory alloy (Ni(2)Mn(1.36)Sn(0.64)): a comparison

The manganite Nd(0.25)Sm(0.25)Sr(0.5)MnO(3) (NSSMO) shows a first-order metal to insulator transition on cooling, which is concomitant with a magnetic transition from the ferromagnetic to antiferromagnetic state. In some respect the sample shows a striking similarity with Ni-Mn-Sn based ferromagnetic shape memory alloys (FSMAs) undergoing a first-order magneto-structural transition, and efforts have been made to highlight the similarities and dissimilarities of the studied manganite with one such FSMA of composition Ni(2)Mn(1.36)Sn(0.64). From our transport and magnetic investigations, the region of transition in the NSSMO is found to be highly metastable, with a clear indication of a magnetically arrested state which persists even when the sample is cooled down to the lowest temperature of measurement. Interestingly, the studied manganite shows an inverse magnetocaloric effect similar to the FSMA. However, a striking difference between the two compositions is evident in the low-temperature magneto-transport behavior: while a clear signature of tunneling magnetoresistance is present in NSSMO due to the coexisting metallic and insulating clusters of nanometer dimension, the studied FSMA do not show such behavior due to the absence of any insulating phase in the intermetallic alloy.     

Phase transformation in Ni–Mn–Sn ferromagnetic shape memory alloy thin films induced by dense ionization

The effects of 200 MeV Au ions irradiation on the structural and magnetic properties of Ni–Mn–Sn ferromagnetic shape memory alloy (FSMA) thin films have been systematically investigated. In order to understand the role of initial microstructure and phase of the film with respect to high energy irradiation, the two types of Ni–Mn–Sn FSMA films having different phases at room temperature were irradiated, one in martensite phase (Ni_58.9Mn_28.0Sn_13.1) and other in austenite phase (Ni₅₀Mn_35.6Sn_14.4). Transmission electron microscope (TEM) and scanning electron microscope (SEM) images along with the diffraction patterns of X-rays and electrons confirm that martensite phase transforms to austenite phase at a fluence of 6×10¹² ions/cm² and a complete amorphization occurs at a fluence of 3×10¹³ ions/cm², whereas ion irradiation has a minimal effect on the austenitic structure (Ni₅₀Mn_35.6Sn_14.4). Thermo-magnetic measurements also support the above mentioned behaviour of Ni–Mn–Sn FSMA films with increasing fluence of 200 MeV Au ions. The results are explained on the basis of thermal spike model considering the core and halo regions of ion tracks in FSMA materials.     

NMR and magnetization study of the mixed systems (Pd1-xCux)2 MnIn and (Pd1-xNix)2 MnIn

Systematic NMR and magnetization data with concentration show that for decreasing x these systems go from ferromagnetic (F) to anti-ferromagnetic (AF) order by passing a mixed phase region where both magnetic orders coexist in different domains. The magnetic phase diagrams for both alloy series are nearly coincident. The NMR spectra show that the Cu or Ni atoms substitute randomly onto Pd sites and we find no evidence that the participation of Mn atoms in F or AF domains is at all correlated with their nearest neighbour environments. In the limit where the AF order becomes largely dominant the samples exhibit a magnetic anisotropy after field cooling.     

Transformation behavior of Ni-Mn-Ga in the low-temperature limit

The magnetic, magnetocaloric and thermal characteristics have been studied in a Ni(50.3)Mn(20.8)Ga(27.6)V(1.3) ferromagnetic shape memory alloy (FSMA) transforming martensitically at around 40?K. The alloy shows first a transformation from austenite to an intermediate phase and then a partial transformation to an orthorhombic martensite, all the phases being ferromagnetically ordered. The thermomagnetization dependences enabled observation of the magnetocaloric effect in the vicinity of the martensitic transformation (MT). The Debye temperature and the density of states at the Fermi level are equal to θ(D)?=?(276?±?4)?K and 1.3?states/atom?eV , respectively, and scarcely dependent on the magnetic field. The MT exhibited by Ni-Mn-Ga FSMAs at very low temperatures is distinctive in the sense that it is accompanied by a hardly detectable entropy change as a sign of a small driving force. The enhanced stability of the cubic phase and the low driving force of the MT stem from the reduced density of states near the Fermi level.     

The field and temperature dependence of the magnetic and structural properties of the shape memory compound Ni(1.84)Mn(1.64)In(0.52)

Magnetization and high resolution neutron powder diffraction measurements have been made on the magnetic shape memory alloy Ni(1.84)Mn(1.64)In(0.52). The compound undergoes a broad structural phase transition, which on heating starts at ～150?K and finishes at ～215?K. On cooling there is a ～20?K hysteresis. The high temperature parent phase is cubic (a?=?5.988??) with the L2(1) structure in which the excess Mn atoms occupy the vacancies on the Ni and In sites. The magnetic moment is located mainly on the Mn atoms with the same magnitude on both the 4a (Mn) and 4b (In) sites. The low temperature martensite is monoclinic with parameters a?=?4.405(2), b?=?5.553(2), c?=?12.950(2)??, β?=?86.47(10)°?and space group P2/m. The magnetic properties of the martensitic phase are complex and indicate metamagnetic behaviour.     

Ni2MnGa(100) ferromagnetic shape memory alloy: A surface study

Ni₂MnGa(100) single crystal studied using low energy electron diffraction (LEED) and ultraviolet photoemission spectroscopy (UPS) exhibits interesting modification of the surface properties that are mainly influenced by surface composition as well as intrinsic effects. In the martensite phase, the LEED spot profiles show presence of an incommensurate modulation for the stoichiometric surface. In contrast, a commensurate modulation is observed for Mn-excess Ni–Mn–Ga surface. A pre-martensite phase is identified at the surface. Both the surface martensitic and pre-martensitic transition temperatures decrease as the Mn content increases. The UPS spectra in the austenite phase exhibit systematic change in shape as a function of surface composition that can be related to changes in the hybridization between Ni and Mn 3d states. The spectra in the martensite phase exhibit interesting modifications near the Fermi level, which has been compared to density of states calculated for a modulated structure by ab-initio density functional theory. Intrinsic surface properties dissimilar from the bulk are enhanced hysteresis width of the martensite transition and increased pre-martensitic transition temperature.     

Tuning the phase transition dynamics by variation of cooling field and metastable phase fraction in Al doped Pr(0.5)Ca(0.5)MnO(3)

We report the effect of field, temperature and thermal history on the time dependence in resistivity and magnetization in the phase separated state of Al doped Pr(0.5)Ca(0.5)MnO(3). The rate of time dependence in resistivity is much higher than that of magnetization and it exhibits a different cooling field dependence due to percolation effects. Our analysis shows that the time dependence in physical properties depends on the phase transition dynamics, which can be effectively tuned by variation of temperature, cooling field and metastable phase fraction. The phase transition dynamics can be broadly divided into the arrested and unarrested regimes, and in the arrested regime this dynamics is mainly determined by time taken in the growth of critical nuclei. An increase in cooling field and/or temperature shifts this dynamics from the arrested to unarrested regime, and in this regime, this dynamics is determined by the thermodynamically allowed rate of formation of critical nuclei, which in turn depends on the cooling field and available metastable phase fraction. At a given temperature, a decrease in metastable phase fraction shifts the crossover from arrested to unarrested regimes towards lower cooling field. It is rather significant that in spite of the metastable phase fraction calculated from resistivity being somewhat off that of magnetization, their cooling field dependence exhibits a striking similarity, which indicates that the dynamics in arrested and unarrested regimes are so different that it comes out vividly provided that the measurements are performed around the percolation threshold.     

Magnetic domains perpendicular to the AC demagnetizing field in ordered Ni3Mn

Stripe domains with walls perpendicular to the AC demagnetizing field (PACD) are observed in atomically ordered, ferromagnetic NiMn with slightly more than 25 at.% Mn. Based on Lorentz microscopy and magnetic measurements. PACD is explained in terms of an inhomogeneity in the magnetic phase and coherent rotation of the magnetization in the domain.     

Effects of the Mn/Co ratio on the magnetic transition and magnetocaloric properties of Mn1+xCo1-xGe alloys

We have investigated the magnetic transition and magnetocaloric effects of Mn 1+x Co 1 x Ge alloys by tuning the ratio of Mn/Co.With increasing Mn content,a series of first-order magnetostructural transitions from ferromagnetic to paramagnetic states with large changes of magnetization are observed at room temperature.Further increasing the content of Mn (x=0.11) gives rise to a single second-order magnetic transition.Interestingly,large low-field magnetic entropy changes with almost zero magnetic hysteresis are observed in these alloys.The effects of Mn/Co ratio on magnetic transition and magnetocaloric effects are discussed in this paper.     

Optimization of Pr(0.9)Ca(0.1)MnO(3) thin films and observation of coexisting spin-glass and ferromagnetic phases at low temperature

Optimization of thin films of small bandwidth manganite, Pr(1-x)Ca(x)MnO3 (for x = 0.1), and their magnetic properties are investigated. Using different pulsed laser deposition (PLD) conditions, several films were deposited from the stoichiometric target material on SrTiO3 (001) substrate and their thorough structural and magnetic characterizations were carried out using x-ray diffraction, atomic force microscopy, x-ray photoelectron spectroscopy (XPS), SQUID magnetometry and ac susceptibility measurements. A systematic investigation shows that irrespective of the growth temperature (between 550 and 750?°C), all the as-deposited films have twin boundaries and magnetic double phases. Post-annealing in partial or full oxygen pressure removes the extra phase and the twin boundaries. Zero-field-cooled magnetization data show an antiferromagnetic to paramagnetic transition at around 100 K whereas the field-cooled magnetization data exhibit a paramagnetic to ferromagnetic transition close to 120 K. However, depending on the oxygen treatments, the saturation magnetization and Curie temperature of the films change significantly. Redistribution of oxygen vacancies due to annealing treatments leading to a change in ratio of Mn3+ and Mn4+ in the films is observed from XPS measurements. Low temperature (below 100 K) dc magnetization of these films shows metamagnetic transition, high coercivity and irreversibility magnetizations, indicating the presence of a spin-glass phase at low temperature. The frequency dependent shift in spin-glass freezing temperature from ac susceptibility measurement confirms the coexistence of spin-glass and ferromagnetic phases in these samples at low temperature.     

Structure, magneto-structural transitions and magnetocaloric properties in Ni50−xMn37+xIn13 melt spun ribbons

Melt spun Ni_50−xMn_37+xIn₁₃ (2≤x≤5) ribbons were investigated for the structure, microstructure, magneto-structural transitions and inverse magnetocaloric effect (IMCE) associated with the first-order martensitic phase transition. The influence of excess Mn in Ni site (or Ni/Mn content) on the martensite transition and the associated magnetic and magnetocaloric properties are discussed. It was found that with the increase in Mn content, the martensitic transition shifted from 325 to 240 K as x is varied from 2 to 4, and the austenite phase was stabilized at room temperature. The x=5 ribbon did not show the martensitic transition. For the x=3 ribbon, the structural and magnetic transitions are close together unlike in the x=4 ribbon in which they are far (∼60 K) apart. The zero field cooled and field cooled curves support the presence of exchange bias blocking temperature due to antiferromagnetic interactions in the ribbons. A large change in the magnetization between the martensite and austenite phases was observed for a small variation in the Ni/Mn content, which resulted in large IMCE. A large positive magnetic entropy change (ΔS_M) of 32 J/kg K at room temperature (∼ 300 K) for a field change of 5 T with a net refrigeration capacity of 64 J/kg was obtained in the Ni₄₇Mn₄₀In₁₃ ribbon.     

Large low-field inverse magnetocaloric effect near room temperature in Ni50−x Mn37+x In13 Heusler alloys

Low field inverse magnetocaloric effect (IMCE) associated with first-order martensitic transition in Ni_50−x Mn_37+x In₁₃ (x=3,4,5) alloys was investigated. By tuning the composition of Ni/Mn, large change in the magnetization occurring between martensite and austenite phases in a narrow temperature interval was achieved, which results in large IMCE. Under low magnetic field change of 2 T, a large positive magnetic entropy change (ΔS _M ) of 23.5 J/kg K with a net refrigeration capacity of 53 J/kg was obtained near room temperature (308 K) in the x=3 alloy. The results show that a small variation in Ni/Mn ratio significantly influences the martensitic transition temperature and the associated magnetic and magnetocaloric properties.     

Tunneling anisotropic magnetoresistance in multilayer-(Co/Pt)/AlO_(x)/Pt structures

We report observations of tunneling anisotropic magnetoresitance (TAMR) in vertical tunnel devices with a ferromagnetic multilayer-(Co/Pt) electrode and a nonmagnetic Pt counterelectrode separated by an AlOx barrier. In stacks with the ferromagnetic electrode terminated by a Co film the TAMR magnitude saturates at 0.15% beyond which it shows only weak dependence on the magnetic field strength, bias voltage, and temperature. For ferromagnetic electrodes terminated by two monolayers of Pt we observe order(s) of magnitude enhancement of the TAMR and a strong dependence on field, temperature and bias. The discussion of experiments is based on relativistic ab initio calculations of magnetization orientation dependent densities of states of Co and Co/Pt model systems.