Magnetic properties and magnetocaloric effects in amorphous and crystalline Gd55Co35Ni10 ribbons

The magnetic properties and magnetocaloric effects of amorphous and crystalline Gd55Co35Ni10 ribbons are investigated.A main phase with a Ho 12 Co 7-type monoclinic structure(space group P21/c) and a minor phase with a Ho4Co3-type hexagonal structure(space group P63/m) are obtained for crystalline ribbon after annealing.The amorphous ribbons order ferromagnetically and undergo a second-order transition at 192 K.For crystalline Gd55Co35Ni10 ribbons,two magnetic phase transitions occur at 158 and 214 K,respectively.The peak value of-△SM under a field change of 0-5 T is 6.5 J/kg K at 192 K for amorphous Gd55Co35Ni10 ribbons.A relatively large magnetic entropy change(～5.0 J/kg K) under a field change of 0-5 T for the crystalline Gd55Co35Ni10 ribbons is obtained in the temperature interval range of 154-214 K.The large platform of magnetic entropy change and the negligible thermal/magnetic hysteresis loss mean the crystalline Gd55Co35Ni10 compound can satisfy the requirement of the Ericsson-type refrigerator working in the temperature range from 154K to 214K.     

Structure,magnetic properties and magnetocaloric effects of Fe50Mn15−x Co x Ni35 alloys

Fe50Mn15-xCoxNi35(x=0,1,3,5,7)alloys were prepared by arc melting under purified argon atmosphere.The ingots were homogenized at 930°C for 90h followed by water quenching.The crystal structure,magnetic properties and magnetocaloric effects of the alloys were studied by X-ray diffraction(XRD)and MPMS-7-type SQUID.The results show that all samples still maintained a single-(Fe,Ni)-type phase structure.With the increase of the content of Co,the Curie temperatures of these alloys increased and exhibited a second-order magnetic transition from ferromagnetic(FM)to paramagnetic(PM)state near Curie temperature.The maximum magnetic entropy change and the relative cooling power of Fe50Mn10Co5Ni35alloy was 2.55 J/kg·K and 181 J/kg,respectively,for an external field change of 5T.Compared with rare earth metal Gd,Fe50Mn15-xCoxNi35 series of alloys have obvious advantage in resource price;their Curie temperatures can be tuned to near room temperature,maintain a relatively large magnetic entropy change at the same time and they are a type of potential magnetic refrigeration materials near room temperature.     

Magnetic entropy change and magnetic phase transition of LaFe11.4Al1.6Cx （x=0-0.8） compounds

The unit cell volume and phase transition temperature of LaFe11.4Al1.6Cx compounds have been studied. The magnetic entropy change, refrigerant capacity and the type of magnetic phase transition are investigated in detail for LaFe11.4Al1.6Cx with x=0.1, All the LaFe11.4Al1.6Cx （x=0-0.8） compounds have the cubic NaZn13-type structure. The addition of carbon atoms brings about a considerable increase in the lattice parameter. The bulk expansion results in the change of phase transition temperature （Tc）, Tc increases from 187K to 269 K with x varying from 0.1 to 0.8, Meanwhile an increase in the lattice parameter can also cause a change of the magnetic ground state from antiferromagnetic to ferromagnetic. Large magnetic entropy change IASI is found over a large temperature range around Tc and the refrigerant capacity is about 322J/kg for LaFe11.4Al1.6C0.1. The magnetic phase transition belongs in weakly first-order one for x=0.1.     

Giant magnetocaloric effect in the Gd5Ge2.025Si1.925In0.05 compound

The magnetocaloric properties of the Gd 5 Ge 2.025 Si 1.925 In 0.05 compound have been studied by x-ray diffraction,magnetic and heat capacity measurements.Powder x-ray diffraction measurement shows that the compound has a dominant phase of monoclinic Gd5Ge2Si2-type structure and a small quantity of Gd 5(Ge,Si) 3-type phase at room temperature.At about 270 K,this compound shows a first order phase transition.The isothermal magnetic entropy change(△SM) is calculated from the temperature and magnetic field dependences of the magnetization and the temperature dependence of MCE in terms of adiabatic temperature change(△Tad) is calculated from the isothermal magnetic entropy change and the temperature variation in zero-field heat-capacity data.The maximum S M is 13.6 J·kg-1·K-1 and maximum △Tad is 13 K for the magnetic field change of 0-5 T.The Debye temperature(θD) of this compound is 149 K and the value of DOS at the Fermi level is 1.6 states/eV·atom from the low temperature zero-field heat-capacity data.A considerable isothermal magnetic entropy change and adiabatic temperature change under a field change of 0-5 T jointly make the Gd5Ge2.025Si1.925 In 0.05 compound an attractive candidate for a magnetic refrigerant.     

Large magnetoresistance in metamagnetic CoMnSi0.88Ge0.12 alloy

The magneto-transport properties are investigated in metamagnetic CoMnSi0.88Ge0.12 alloy.By applying a magnetic field or increasing temperature,a metamagnetic phase transition from antiferromagnetic to ferromagnetic is observed in this alloy.Around the metamagnetic phase transition,CoMnSi0.88Ge0.12 alloy exhibits a large and negative magnetoresistance effect(～32%) under a magnetic field of 20 kOe(1 Oe = 79.5775 A/m),which is ascribed to the spin-dependent scattering of conduction electrons.     

Large Barocaloric Effect with High Pressure-Driving Efficiency in a Hexagonal MnNi_(0.77)Fe_(0.23)Ge Alloy

The hydrostatic pressure is expected to be an effective knob to tune the magnetostructural phase transitions of hexagonal MM'X alloys(M and M' denote transition metals and X represents main group elements).We perform magnetization measurements under hydrostatic pressure on an MM'X martensitic MnNi_(0.77)Fe_(0.23)Ge alloy.The magnetostructural transition temperature can be efficiently tuned to lower temperatures by applying moderate pressures,with a giant shift rate of-151 K/GPa.A temperature span of 30 K is obtained under the pressure,within which a large magnetic entropy change of-23 J·kg~(-1)K~(-1) in a field change of 5 T is induced by the mechanical energy gain due to the large volume change.Meanwhile,a decoupling of structural and magnetic transitions is observed at low temperatures when the martensitic transition temperature is lower than the Curie temperature.These results show a multi-parameter tunable caloric effect that benefits the solid-state cooling.     

Effect of Dy substitution on magnetic properties and magnetocaloric effects of Tb6Co1.67Si3 compounds

The magnetic and magnetocaloric properties of(Tb1-xDyx) 6 Co 1.67 Si 3(0 ≤ x ≤ 0.8) have been experimentally investigated.The compounds exhibit a Ce6Ni2Si3-type hexagonal structure and undergo a second-order magnetic transition.The Curie temperature decreases from ～ 187 K to 142 K as the content of Dy grows from 0 to 0.8.The maximal magnetic entropy change,for a field change of 0-5 T,varies between ～ 6.2 and ～ 7.4 J/kg.K,slightly decreasing when Dy is introduced.The substitution of Dy leads to a remarkable increase in refrigeration capacity(RC).A large RC value of ～ 626 J/kg is achieved for x = 0.4 under a field change of 0-5 T.     

Magnetic entropy change and large refrigerant capacity of Ce6Ni2Si3-type GdCoSiGe compound

Magnetic entropy change (△S M) and refrigerant capacity (RC) of Ce 6 Ni 2 Si 3-type Gd 6 Co 1.67 Si 2.5 Ge 0.5 compounds have been investigated.The Gd 6 Co 1.67 Si 2.5 Ge 0.5 undergoes a reversible second-order phase transition at the Curie temperature T C=296 K.The high saturation magnetization leads to a large △S M and the maximal value of △S M is found to be 5.9 J/kg · K around T C for a field change of 0-5 T.A broad distribution of the △S M peak is observed and the full width at half maximum of the △S M peak is about 101 K under a magnetic field of 5 T.The large RC is found around T C and its value is 424 J/kg.     

Magnetic properties and magnetocaloric effect in compound PrFe12B6

Magnetic properties and magnetocaloric effect of compound PrFe 12 B 6 are investigated.The coexistence of hard phase PrFe 12 B 6 and soft phase α-Fe causes interesting phenomena on the curves for the temperature dependence of magnetization.PrFe 12 B 6 experiences a first order phase transition at the Curie temperature 200 K,accompanied by an obvious lattice contraction,which in turn results in a large magnetic entropy change.The Maxwell relation fails to give the correct information about magnetic entropy change due to the first order phase transition nature.The large magnetic entropy changes of PrFe 12.3 B 4.7 obtained from heat capacity method are 11.7 and 16.2 J/kg.K for magnetic field changes of 0-2 T and 0-5 T respectively.     

Magnetic properties and in compound magnetocaloric effect PrFe12B6

Magnetic properties and magnetocaloric effect of compound PrFe12B6 are investigated. The coexistence of hard phase PrFe12B6 and soft phase α-Fe causes interesting phenomena on the curves for the temperature dependence of magnetization. PrFe12B6 experiences a first order phase transition at the Curie temperature 206 K, accompanied by an obvious lattice contraction, which in turn results in a large magnetic entropy change. The Maxwell relation fails to give the correct information about magnetic entropy change due to the first order phase transition nature. The large magnetic entropy changes of PrFe12.3B4.7 obtained from heat capacity method are 11.7 and 16.2 J/kg.K for magnetic field changes of 0-2 T and 0-5 T respectively.     

Pressure effects on magnetic properties and martensitic transformation of Ni–Mn–Sn magnetic shape memory alloys

The mechanism for the effects of pressure on the magnetic properties and the martensitic transformation of Ni-Mn- Sn shape memory alloys is revealed by first-principles calculations. It is found that the total energy difference between paramagnetic and ferromagnetic austenite states plays an important role in the magnetic transition of Ni-Mn-Sn under pressure. The pressure increases the relative stability of the martensite with respect to the anstenite, leading to an increase of the martensitic transformation temperature. Moreover, the effects of pressure on the magnetic properties and the martensitic transformation are discussed based on the electronic structure.     

Evolution of magnetic domain structure of martensite in Ni–Mn–Ga films under the interplay of the temperature and magnetic field

Ferromagnetic shape memory Ni-Mn-Ga films with 7M modulated structure were prepared on MgO （001） substrates by magnetron sputtering. Magnetization process with a typical two-hysteresis loop indicates the occurrence of the reversible magnetic field-induced reorientation. Magnetic domain structure and twin structure of the film were controlled by the in- terplay of the magnetic and temperature field. With cooling under an out-of-plane magnetic field, the evolution of magnetic domain structure reveals that martensitic transformation could be divided into two periods： nucleation and growth. With an in-plane magnetic field applied to a thermomagnetic-treated film, the evolution of magnetic domain structure gives evidence of a reorientation of twin variants of martensite. A microstructural model is described to define the twin structure and to produce the magnetic domain structure at the beginning of martensitic transformation; based on this model, the relationship between the twin structure and the magnetic domain structure for the treated film under an in-plane field is also described.     

Transformation behaviors,structural and magnetic characteristics of Ni-Mn-Ga films on MgO （001）

Ferromagnetic Ni-Mn-Ga films were fabricated by depositing on MgO （001） substrates at temperatures from 673 K to 923 K. Microstructure, crystal structure, martensitic transformation behavior, and magnetic properties of the films were studied. With increasing deposition temperature, the surface morphology of the films transforms from granular to continu- ous. The martensitic transformation temperature is not dependent on deposition temperature; while transformation behavior is affected substantially by deposition temperature. X-ray analysis reveals that the film deposited at 873 K has a 7M marten- site phase, and its magnetization curve provides a typical step-increase, indicating the occurrence of magnetically induced reorientation （MIR）. In situ magnetic domain structure observation on the film deposited at 873 K reflects that the marten- sitic transformation could be divided into two periods： nucleation and growth, in the form of stripe domains. The MIR occurs at the temperature at which martensitic transformation starts, and the switching field increases with the decrease of temperature due to damped thermal activation. The magnetically induced martensitic transformation is related to the difference of magnetization between martensite and austenite. A shift of martensite temperature of dT/dH = 0.43 K/T is observed, consistent with the theoretical value, 0.41 K/T.     

The influence of Al substitution on the phase transitions and magnetocaloric effect in Ni43Mn46Sn11−xAlx alloys

The effects of Al substitution on the phase transitions and magnetocaloric effect of Ni₄₃Mn₄₆Sn_11−xAl_x (x=0-2) ferromagnetic shape memory alloys were investigated by X-ray diffraction and magnetization measurements. With the increase of Al content, the cell volume decreases due to the smaller radius of Al, and the martensitic transformation temperature increases rapidly, while the Curie temperature of austenitic phase shows a small increase. A large positive and a negative magnetic entropy change were observed near the first-order martensitic transition and the second-order magnetic transition, respectively. The magnetic entropy changes, hysteresis behavior, and refrigerant capacity near the two transitions are compared.     

Effect of Sb-doping on martensitic transformation and magnetocaloric effect in Mn-rich Mn_(50)Ni_(40)Sn_(10-x)Sb_x(x=1,2,3,and 4) alloys

We investigate the influence of Sb-doping on the martensitic transformation and magnetocaloric effect in Mn_(50)Ni_(40)Sn_(10-x)Sb_x(x = 1, 2, 3, and 4) alloys. All the prepared samples exhibit a B2-type structure with the space group F m3 m at room temperature. The substitution of Sb increases the valence electron concentration and decreases the unit cell volume. As a result, the magnetostructural transformation shifts rapidly towards higher temperatures as x increases.The changes in magnetic entropy under different magnetic field variations are explored around this transformation. The isothermal magnetization curves exhibit typical metamagnetic behavior, indicating that the magnetostructural transformation can be induced by a magnetic field. The tunable martensitic transformation and magnetic entropy changes suggest that Mn_(50)Ni_(40)Sn_(10-x)Sb_x alloys are attractive candidates for applications in solid-state refrigeration.     

Giant low-field magnetocaloric effect in EuTi(1-x)NbxO3(x = 0.05, 0.1, 0.15, and 0.2) compounds

The magnetic properties and magnetocaloric effect(MCE)of EuTi(1-x)NbxO3(x=0.05,0.1,0.15,and 0.2)compounds are investigated.Owing to electronic doping,parts of Ti ions are replaced by Nb ions,the lattice constant increases and a small number of Ti⁴⁺(3d^0)ions change into Ti³⁺(3d^1).It is the ferromagnetism state that is dominant in the derivative balance.The values of the maximum magnetic entropy change(-?SM^max)are 10.3 J/kg·K,9.6 J/kg·K,13.1 J/kg·K,and 11.9 J/kg·K for EuTi(1-x)NbxO3(x=0.05,0.1,0.15,and 0.2)compounds and the values of refrigeration capacity are 36,33,86,and 80 J/kg as magnetic field changes in a range of 0 T–1 T.The EuTi(1-x)NbxO3(x=0.05,0.1,0.15,and 0.2)compounds with giant reversible MCE are considered as a good candidate for magnetic refrigerant working at lowtemperature and low-field.     

Effects of pre-deformation on the martensitic transformation and magnetocaloric property in Ni-Mn-Co-Sn ribbons

This paper investigates the martensitic transformation and magnetocaloric effect in pre-deformed Ni-Mn-Co-Sn ribbons.The experimental results show that the reverse martensitic transformation temperature T M increases with the increasing pre-pressure,suggesting that pre-deformation is another effective way to adjust T M in ferromagnetic shape memory alloys.Large magnetic entropy changes and refrigerant capacities are obtained in these ribbons as well.It also discusses the origin of the enhanced martensitic transformation temperature and magnetocaloric property in pre-deformed Ni-Mn-Co-Sn ribbons.     

Relation between martensitic transformation temperature range and lattice distortion ratio of NiMnGaCoCu Heusler alloys

In order to study the relation between martensitic transformation temperature range AT （where AT is the difference between martensitic transformation start and finish temperature） and lattice distortion ratio （c/a） of martensitic transforma~ tion, a series of Ni46Mnz8_xGa22Co4Cux （x = 2-5） Heusler alloys is prepared by arc melting method. The vibration sample magnetometer （VSM） experiment results show that AT increases when x 〉 4 and decreases when x 〈 4 with x increasing, and the minimal AT （about 1 K） is found at x = 4. Ambient X-ray diffraction （XRD） results show that AT is proportional to c/a for non-modulated Ni46Mn28_xGa22Co4Cux （x = 2-5） martensites. The relation between AT and c/a is in agreement with the analysis result obtained from crystal lattice mismatch model. About 1000-ppm strain is found for the sample at x = 4 when heating temperature increases from 323 K to 324 K. These properties, which allow a modulation of AT and temperature-induced strain during martensitic transformation, suggest Ni46Mn24Ga22Co4Cu4 can be a promising actuator and sensor.