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Magnetic refrigeration technology based on the magnetocaloric effect (MCE) of magnetic substances has been considered a prominent, energy‐efficient, and environmentally benign cooling method. Exploring suitable magnetic substances is a prerequisite for practical applications. A family of rare‐earth‐free magnetocaloric materials called Mn30Fe20−xCuxAl50 alloys is identified room‐temperature refrigeration, which are derived from the well‐known MnAl‐based permanent magnets. As expected from experimental and theoretical investigations, all of the Mn30Fe20−xCuxAl50 alloys are crystallized in a stable cubic CsCl‐type crystal structure, revealing a single second‐order type magnetic phase transition (MPT) with tunable MPT temperature. They also exhibit a large reversible MCE and good magnetocaloric performances in a wide temperature range. Crucially, these Mn30Fe20−xCuxAl50 alloys represent a rare case of magnetic materials belonging to a large family that can be fabricated from low‐price, earth‐abundant, and non‐toxic elements. They could provide new choices for practical room‐temperature magnetic refrigeration applications. [ABSTRACT FROM AUTHOR]

Rare-earth based amorphous alloys with promising glass forming ability (GFA) and considerable magnetocaloric effect (MCE) are extensively exploited for magnetic refrigeration (MR) materials. Here, the GFA, magnetic properties, MCE, and refrigeration performance of RE60Al20Ni20 (RE = Tm, Er, and Ho) amorphous ribbons were investigated. A magnetic phase transition (paramagnetic to ferromagnetic, second-order) with ignorable field and thermal hysteresis was found around TC ∼ 4.4 K for Tm60Al20Ni20, ∼9.5 K for Er60Al20Ni20, and ∼17.9 K for Ho60Al20Ni20. For a field change ΔH = 50 kOe, the MCE parameters of the maximal magnetic entropy change (around their own TC) and relative cooling power are 14.1 J/kg K and 235 J/kg for Tm60Al20Ni20, 14.3 J/kg K and 372 J/kg for Er60Al20Ni20, and 12.4 J/kg K and 460 J/kg for Ho60Al20Ni20. In addition, the temperature averaged entropy change at ΔTlift (temperature span) of 2 K and 5 K is investigated, very close values and similar field dependence with magnetic entropy change indicating that RE60Al20Ni20 (RE = Tm, Er, and Ho) has potential applications in cryogenic magnetic refrigeration. [ABSTRACT FROM AUTHOR]

The intermetallic gallium compounds RE2Co2Ga with different rare earths (RE = Dy, Ho, Er, and Tm) were synthesized, and their crystal structure, microstructure, magnetic, and cryogenic magneto-caloric performances were investigated. The RE2Co2Ga compounds crystallize with an ordered orthorhombic W2B2Co-type structure (space group Immm). All the RE2Co2Ga compounds undergo ferromagnetic (FM) ordering (second-order) from a paramagnetic to FM transition which induces reversible magneto-caloric effects (MCE). The Curie temperatures (TC) in RE2Co2Ga compounds are determined to be 55.0, 38.5, 25.5, and 11.6 K for RE = Dy, Ho, Er, and Tm, respectively, which fulfill the de Gennes scaling. The RE2Co2Ga compounds show relatively small MCE (i.e., −ΔSM, isothermal magnetic entropy change) around their own phase transition temperatures, and the maximal values of −ΔSM are 7.5, 14.6, 11.2, and 13.2 J/kg K in the field change (ΔH) of 7 T for RE = Dy, Ho, Er, and Tm, respectively. Accordingly, the values of the relative cooling power are 212, 335, 304, and 239 J/kg, respectively. [ABSTRACT FROM AUTHOR]

In this paper, a detailed investigation with respect to the structural, cryogenic magnetic properties and magnetocaloric performances of RE 2 CuMnO 6 (RE = Gd, Dy, Ho and Er) double perovskite (DP) compounds has been performed. All the RE 2 CuMnO 6 compounds are confirmed to B -site disordered and crystallized in the GdFeO 3 -type structure (Pnma space group, N 62, oP20). The magnetic transition temperatures (T M) are found to be ~7.5 K for Gd 2 CuMnO 6 , ~12.1 K for Dy 2 CuMnO 6 , ~12.2 K for Ho 2 CuMnO 6 , and ~3.6 K for Er 2 CuMnO 6 , respectively. Moreover, for checking the magnetocaloric performances several vital parameters including -Δ S M max (peak value of magnetic entropy change, -Δ S M), TEC (3) (temperature averaged -Δ S M) and RCP (relative cooling powers) are evaluated to be 7.84, 7.73 J/kgK and 151.1 J/kg for Gd 2 CuMnO 6 , 5.69, 5.59 J/kgK and 180.9 J/kg for Dy 2 CuMnO 6 , 7.12, 7.05 J/kgK and 192.4 J/kg for Ho 2 CuMnO 6 , as well as 9.92, 9.60 J/kgK and 195.9 J/kg for Er 2 CuMnO 6 under the magnetic field change Δ H = 5 T, respectively. [ABSTRACT FROM AUTHOR]

The magnetic cooling utilizing magneto-caloric effect is recognized as promising energy efficiency and environmentally friendly technology. Here we report a systematical study on the microstructures, magnetic properties and cryogenic magneto-caloric performances of the Gd20Ho20Tm20Cu20Ni20 amorphous ribbons. It is found that the ribbons reveal a second-order phase transition and are accompanied by a table-shaped magneto-caloric effect. The calculated magnetic-entropy-change maximum |ΔSM|, temperature averaged entropy change (i.e., TEC(10)), and refrigerant capacity reach 13.9 J/kg⋅K, 13.84 J/kg⋅K and 740 J/kg with magnetic field change of 0–7 T, respectively, indicating that the present Gd20Ho20Tm20Cu20Ni20 amorphous ribbons are good candidates for magnetic cooling. [ABSTRACT FROM AUTHOR]

Nowadays, magnetic cooling (MC) technology by using the magnetocaloric effect (MCE) has attracted extensive research interest for its promising practical applications. A constant large/giant MCE covers wide refrigeration temperatures (denote as table-like shape) is beneficial for obtaining high efficiency performance for MC. In this paper, the HoNi/HoNi2 composite was successfully synthesized by arc-melting method and proved to be composed of HoNi and HoNi2 crystalline phases with weight ratios of 52.4 wt.% and 47.6 wt.%, respectively. The maximum magnetic entropy change () is 18.23 J/(kg⋅K), and the refrigerant capacity values RC1, RC2, and RC3 are 867.9 J/kg, 676.4 J/kg, and 467.8 J/kg with ΔH = 0–70 kOe, respectively. The table-like shape MCE and large refrigerant capacity values make the composite attractive for cryogenic MC using the Ericsson cycle. [ABSTRACT FROM AUTHOR]

The microstructure, cryogenic magnetic properties, magneto-caloric effect (MCE) and refrigeration performance of equi-atomic HoErGdCuNi ribbons have been investigated. Fully amorphousized structure with uniform distribution for all constituent elements is obtained. A table-like MCE that covers the temperature region from liquid nitrogen to liquid hydrogen is observed, which leads to a giant refrigerant capacity. Accordingly, the maximum magnetic entropy change (- Δ S M max) , temperature-averaged entropy change [ TEC (10)] and refrigerant capacity (RC) are 15.8 J/kgK, 15.7 J/kgK and 903 J/kg, respectively, at the magnetic field change (Δ H) of 0–7 T. The equi-atomic HoErGdCuNi amorphous ribbons with good MCE parameters especially those with large RC values, are an attractive candidate for cryogenic magnetic refrigeration materials. • Magnetism and magnetocaloric effect (MCE) of HoErGdCuNi ribbons were investigated. • A giant refrigerant capacity (RC) in HoErGdCuNi ribbons was obtained. • The origin of MCE and its potential application in HoErGdCuNi were discussed. [ABSTRACT FROM AUTHOR]

Abstract It is well known that rare earth (RE) based intermetallic compounds reveal various interesting magnetic properties depending on the crystallized structures and the constituent elements, paving the way for potential applications in different fields. Recent progresses regarding magnetic properties and magnetocaloric effect (MCE) in ternary rare earth RE 2 T 2 X (RE = Gd-Tm; T = Cu, Ni, Co; and X = Cd, In, Ga, Sn, Al) intermetallic compounds are reviewed in this paper. Some of them exhibit excellent MCE performances which make them attractive in the field of magnetic refrigeration at low temperature. With the aim of understanding the magnetocaloric characteristics of RE 2 T 2 X compounds, the crystal structure, magnetism and magnetic phase transition are also focused. The origin of the MCE together with the physics behind and the potential application of RE 2 T 2 X compounds are thoroughly considered. Highlights • Magnetic and magnetocaloric properties in RE 2 T2X compounds are reviewed. • The RE 2 T2X compounds show four types of crystallize structures. • Some of them exhibit excellent cryogenic magnetocaloric performances. • The origin of magnetocaloric effect in RE 2 T2X compounds is discussed. [ABSTRACT FROM AUTHOR]

Abstract Double perovskite Pr 2 NiMnO 6 (PNMO) and Pr 2 CoMnO 6 (PCMO) ceramics have been synthesized and their crystal structure, microstructure, as well as cryogenic magnetic properties and magnetocaloric performance have been investigated. The crystal structure of PNMO and PCMO ceramics was determined to be monoclinic with space group of P21/n at room temperature. A ferromagnetic to paramagnetic (FM-PM) phase transition (second-order) occurred in PNMO and PCMO around 208 and 170 K, respectively. Significant reversible magnetocaloric effect (MCE) was found and the values of the maximum magnetic entropy change (-Δ S M max) were 3.15 and 3.91 J/kg-K under the magnetic field change (Δ H) of 0–7 T in PNMO and PCMO, respectively. The corresponding relative cooling power (RCP) values were 241.9 and 229.9 J/kg. [ABSTRACT FROM AUTHOR]

[Display omitted] • Ferromagnetic Al-Mn-Fe-Co-Cr high-entropy (HE) alloys were fabricated. • Structural, magnetic and magnetocaloric (MC) properties were reported. • Combined experimentally determined and theoretically analyzed was performed. • Excellent MC properties were achieved at room temperature. • These HE alloys have potential for room temperature magnetic refrigeration. In the present study, the structure, magnetic phase transition, and magnetocaloric performance of Al 20 Mn 20 Fe 20 Co 14.5+ x Cr 25.5- x (x = 0, 1, and 2), a series of typical rare-earth-free high-entropy (HE) alloys, were experimentally determined and theoretically analyzed based on first-principle calculation. Ferromagnetic behavior was established and their Curie temperature could be tuned in a wide temperature range, which correlated with Co content; specifically, it increased from 282.8 K for Co 14.5 Cr 25.5 to 345.8 K for Co 16.5 Cr 23.5. In addition, the electronic density of states and magnetic moments associated with each consistent element were analyzed in the HE alloys. Maximum magnetic entropy changes of 1.135, 1.150, and 1.096 J/kgK were obtained for an x of 0, 1, and 2 under a magnetic field change of 5 T. These values are comparable or superior to those of reported 3 d metal-based HE alloys. Furthermore, the experimental characterizations and theoretical predications agreed well, which provided an in-depth understanding of the rare-earth-free HE Al-Mn-Co-Fe-Cr alloy system, which is expected to be expanded to other systems in the future. [ABSTRACT FROM AUTHOR]

The structure, magnetic transition and magnetocaloric properties in the ternary gallium intermetallic compounds of Ho 2 Ni 2 Ga and Tm 2 Ni 2 Ga have been systematically investigated by using X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive spectroscopy (EDS) and magnetization measurements. As found from powder XRD and Rietveld refinement, Ho 2 Ni 2 Ga and Tm 2 Ni 2 Ga crystallized in an orthorhombic structure of the W 2 B 2 Co type belonging to the Immm space group. Both compounds are ordering antiferromagnetically at low temperatures and under low magnetic fields together with a field-induced metamagnetic transition from antiferromagnetic (AFM) to ferromagnetic (FM). Peculiar and similar magnetocaloric properties are observed for both compounds, i. e., an inverse magnetocaloric effect (positive magnetic entropy change, Δ S M ) under low magnetic field changes (Δ H ) and at low temperatures together with a large normal reversible magnetocaloric effect under high Δ H . The positive Δ S M below/at the Néel temperatures ( T N ) is ascribed to first order transition from antiferromagnetic (AFM) to ferromagnetic (FM) states, whereas the negative Δ S M above T N is due to the fact of the magnetic transition from paramagnetic (PM) to ferromagnetic (FM) states. Based on the field-dependent magnetization data, the maximum magnetic entropy change (−Δ S M max ), relative cooling power ( RCP ) and refrigerant capacity ( RC ) are established, and the corresponding values are 9.6 J/kg K, 276 J/kg and 206 J/kg for Ho 2 Ni 2 Ga, and are 4.3 J/kg K, 60 J/kg and 46 J/kg for Tm 2 Ni 2 Ga, respectively, for a magnetic field change of 0–70 kOe. [ABSTRACT FROM AUTHOR]

Two single-phased aluminide RE NiAl 2 ( RE = Ho and Er) compounds have been synthesized by an arc-melting method. The magnetic properties and magnetocaloric effect (MCE) of HoNiAl 2 and ErNiAl 2 have been studied by magnetization measurements. A second-order paramagnetic (PM) to ferromagnetic (FM) phase transition together with a considerable reversible MCE were observed around the Curie temperature T C ∼7.5 K and 5.0 K for HoNiAl 2 and ErNiAl 2 , respectively. Under the magnetic field change (Δ H ) of 0–5 T, the maximal values of magnetic entropy change, refrigerant capacity and relative cooling power are 14.0 J/kg K, 171 J/kg, 213 J/kg for HoNiAl 2 and 21.2 J/kg K, 267 J/kg, 357 J/kg for ErNiAl 2 , respectively. [ABSTRACT FROM AUTHOR]

We reported the magnetism, magnetic phase transition behavior and magnetocaloric effect of the ternary Dy 2 CuSi 3 and Ho 2 CuSi 3 compounds. A second order magnetic phase transition from a paramagnetic (PM) to ferromagnetic (FM) state around their respective Curie temperatures were confirmed by using the magnetic measurements and rescaled magnetic entropy change curves in both compounds. A large magnetic entropy change was obtained with the absence of thermal and magnetic hysteresis loss in both compounds. The maximal magnetic entropy change (-Δ S M max ) reach 18.3 and 28.3 J/kg K for a magnetic field change of 0–70 kOe in Dy 2 CuSi 3 and Ho 2 CuSi 3 , respectively. The corresponding values of relative cooling power ( RCP ) are evaluated to be 460 J/kg and 627 J/kg, respectively. [ABSTRACT FROM AUTHOR]

The magnetic properties, magnetocaloric effect (MCE) and universal behaviour of ternary Cadmium compounds Gd 2 Cu 2 Cd and Er 2 Cu 2 Cd have been investigated systematically. A second order magnetic phase transition from a paramagnetic to ferromagnetic state is observed for Gd 2 Cu 2 Cd and Er 2 Cu 2 Cd at their own Curie temperatures of T C ∼120 and 36 K, respectively. A large reversible MCE occurs near its own T C for both compounds. The maximum values of magnetic entropy change (−Δ S M max ) are 10.1 and 19.1 J/kg K under a magnetic field change of 0–7 T with no obviously hysteresis loss for Gd 2 Cu 2 Cd and Er 2 Cu 2 Cd, respectively. The corresponding values of refrigerant capacity ( RC ) and relative cooling power ( RCP ) are evaluated to be 386 and 373 J/kg, and to be 525 and 489 J/kg, respectively. The rescaled magnetic entropy change curves collapse onto a single curve for various magnetic fields, further confirming the Gd 2 Cu 2 Cd and Er 2 Cu 2 Cd compounds with the second order phase transition. [ABSTRACT FROM AUTHOR]

The magnetic properties and magnetocaloric effect (MCE) in antiferromagnetic non-superconducting TbNiBC compound have been investigated in detail. Under low magnetic field changes and at low temperatures, the studied compound shows an inverse MCE which is due to the fact of antiferromagnetic ground state, whereas a normal reversible MCE under high magnetic field changes is observed which is related to the field-induced first-order metamagnetic transition from antiferromagnetic to ferromagnetic states. For the magnetic field change of 0-7 T the values of maximal magnetic entropy change ( $-\Delta S_{\mathrm {M}}^{\max } )$ , refrigerant capacity (RC) and relative cooling power (RCP) for the present TbNiBC are evaluated to be 11.1 J/kg/K, 225 J/kg and 296 J/kg, respectively. [ABSTRACT FROM AUTHOR]

The magnetic properties and magnetocaloric effect (MCE) in the ternary intermetallic compound of EuAuGe have been investigated. The compound undergoes a second-order magnetic phase transition at its own Curie temperatures T∼33 K. A large reversible table-like MCE has been observed from 1 to 40 K, which is related to the magnetic field-sensitive magnetic phase transition. For the magnetic field changes of 0-5 and 0-7 T, the maximum values of magnetic entropy change ( $-{\Delta } S_{\mathrm {M}}^{\max }$) are evaluated to be 7.6 and 10.1 J kg K, respectively; the corresponding relative cooling power ( RCP) are 358 and 499 J kg. The present results indicate that the EuAuGe compound is a considerable candidate for low-temperature refrigeration. [ABSTRACT FROM AUTHOR]

The Heusler type Ni–Mn- Z (Z = Ga, ln, Sn, or Sb) alloys with magneto-structural transformations (MSTs) have received widespread research interests due to the exhibition of multifunctional characters. To further understand MSTs and improve the magnetocaloric performance of these alloys, in this work, the Ti doped Ni 48 Cu 2 Mn 36 Sn 14-x Ti x (x = 0, 1, 2, 3) ribbons have been fabricated and systematically determined with regard to the structural, magnetic, and magnetocaloric properties by means of X-ray diffraction (XRD), scanning electron microscope (SEM), differential scanning calorimetry (DSC), and magnetization measurements. All the ribbons are found to crystallize in the ordered cubic L2 1 austenite phases at room temperature and with the equiaxed austenite morphology. With the increasing Ti content, the average grain size and the MST temperature increase but the austenite Curie temperature (T A C) decrease gradually. Moreover, the thermal hysteresis and magnetic hysteresis loss are greatly reduced with the Ti doping. The value of average hysteresis loss (AHL) is reduced from 86 Jkg−1 for Ti0 to 25.5 Jkg−1 for Ti3 ribbon under 7 T. Additionally, enhanced magnetocaloric effect has been observed by Ti-doping. With the magnetic field change (ΔH) of 0–7 T, the largest value of magnetic entropy change reaches 15.4 Jkg−1K−1 (Ti2) among the Ni 48 Cu 2 Mn 36 Sn 14-x Ti x ribbons. The present work indicates that reasonable Ti doping could be a useful way to regulation the MSTs and improve the magnetocaloric performance of the Heusler type Ni–Mn–Sn-based alloys. • The Hesuler type Ni 48 Cu 2 Mn 36 Sn 14-x Ti x (x = 0, 1, 2, 3) ribbons are fabricated. • The structural, magnetic and magnetocaloric properties were investigated. • Ti doping could be a useful way to regulation the MSTs. • Enhanced magnetocaloric performances has been observed by Ti-doping. [ABSTRACT FROM AUTHOR]

The magnetic properties and magnetocaloric effect (MCE) in Dy 2 Cu 2 In compound have been investigated. Dy 2 Cu 2 In undergoes two magnetic phase transitions, a paramagnetic to ferromagnetic (FM) at T C ∼ 49.5 K followed by a spin reorientation (SR) at T SR ∼ 19.5 K. For a magnetic field change of 0–7 T, the maximum values of the magnetic entropy change (−Δ S M max ) are estimated to be 16.5 around T C and 6.7 J/kg K around T SR with a large relative cooling power ( RCP ) value of 617 J/kg. The modified Arrott plots and universal curves of the rescaled Δ S M confirmed that the magnetic phase transitions in Dy 2 Cu 2 In compound belongs the second order phase transitions. The present results may provide some clues to search for new magnetocaloric materials belonging to RE 2 T 2 X system. [ABSTRACT FROM AUTHOR]

The magnetic and magnetocaloric properties in the equiatomic intermetallic compounds of TmZnAl and TmAgAl have been investigated. The compounds undergo a second order magnetic transition from paramagnetic to ferromagnetic state around its own Curie temperatures T C ∼2.8 K and 3.3 K for TmZnAl and TmAgAl, respectively. A considerable reversible magnetocaloric effect (MCE) was observed at low temperature. For a magnetic field change of 7 T, the maximum values of magnetic entropy change (−Δ S M max ) and relative cooling power ( RCP ) are 11.8 J/kg K and 289 J/kg for TmZnAl, respectively, and the corresponding values for TmAgAl are 14.1 J/kg K and 315 J/kg. [ABSTRACT FROM AUTHOR]

The magnetic and magnetocaloric properties in GdNiBC compound have been investigated by magnetization and heat capacity measurements. The compound exhibits a paramagnetic to ferromagnetic transition at TC\sim 15 K. A large reversible magnetocaloric effect has been observed and accompanied by a second-order magnetic phase transition at TC . The maximum magnetic entropy change ( -\Delta SM^{\mathrm {max}} ) and adiabatic temperature change ( \Delta T\mathrm {ad}^{\mathrm {max}} ) are 24.9 J/kg K and 13 K, for a magnetic field change of 0–7 T, respectively. The corresponding relative cooling power is 801 J/kg. [ABSTRACT FROM AUTHOR]

Magnetic properties and magnetocaloric effect (MCE) in ErFeAl and HoFeAl intermetallic compounds have been studied systematically. Both compounds undergo a second order magnetic phase transition from paramagnetic to ferromagnetic state together with a probable spin reorientation transition at low temperature. A considerable reversible magnetocaloric effect was observed around its own Curie temperatures T C ∼55 K and 80 K for ErFeAl and HoFeAl, respectively. For a magnetic field change of 0–7 T, the maximum values of magnetic entropy change (−Δ S M max ) are found to be 8.3 and 9.9 J/kg K for RE = Er and Ho, respectively. The corresponding values of refrigerant capacity ( RC ) are evaluated to be 384 and 647 J/kg. [ABSTRACT FROM AUTHOR]

The magnetocaloric effect (MCE) of quaternary intermetallic compound ErNiBC has been investigated by magnetization and heat capacity measurements. The compound undergoes a paramagnetic (PM) to ferromagnetic (FM) transition at T C ~5 K and the ground state of Er ion forms a Kramer's doublet state. The magnetic transition is found to be second order in nature. The maximum magnetic entropy change (−Δ S M max ) and adiabatic temperature change (Δ T ad max ) of ErNiBC are 24.8 J/kg K and 8.6 K, respectively, for a magnetic field change of 0–50 kOe, and the corresponding refrigerant capacity ( RC ) is 312 J/kg. [ABSTRACT FROM AUTHOR]

Magnetism and magnetocaloric effect in RE AgAl ( RE = Er and Ho) intermetallic compounds have been studied. Both compounds undergo a second order magnetic phase transition from paramagnetic to ferromagnetic state. A large reversible magnetocaloric effect was observed around its own Curie temperatures T C ∼ 14 and 18 K for ErAgAl and HoAgAl, respectively. For a field change of 0–7 T, the maximum magnetic entropy change reaches 13.7 and 13.8 J/kg K for RE = Er and Ho, respectively. The corresponding relative cooling powers are evaluated to be 398 and 525 J/kg. [ABSTRACT FROM AUTHOR]

The magnetic refrigeration (MR) technology by utilizing the magnetocaloric (MC) effects of magnetic solids have been realized to be a promising energy efficiency and environmentally friendly technology. Developing or discovering proper magnetic solids with promising MC performances is one of the most important tasks at present stage since a huge gap still exists between the requirement of practical MR application and the MC performances of the magnetic solids. Herein, we reported a combined theoretical and experimental investigation of the crystal structure together with the magnetic properties, magnetic phase transition (MPT) and MC performances in Gd 2 MgTiO 6 oxide. The Gd 2 MgTiO 6 is confirmed to crystalize in a B -site ordered monoclinic double perovskite (DP) crystal structure. A rather unstable antiferromagnetic (AFM) interaction with large magnetic moment and semi-conductor characteristic with the band gap of 2.977 eV have been confirmed in Gd 2 TiMgO 6 DP oxide at ground state. Giant reversible cryogenic MC effect together with excellent MC performances have been confirmed by a series of the figure of merits including the values of maximum magnetic entropy change (-Δ S M) and refrigerant capacity (RC), which are evaluated to be 46.21 J/kgK and 300.27 J/kg around 3.3 K with the magnetic change of 0–7 T, these values are much better than most of the recently reported famous cryogenic MC materials and the commercialized magnetic refrigerants gadolinium gallium garnet (GGG) as well. The observed excellent MC performances suggest that Gd 2 TiMgO 6 DP oxide is a promising candidate material for cryogenic MR applications. Graphical abstract [Display omitted]. [ABSTRACT FROM AUTHOR]

The rare-earths (RE) based amorphous materials with large magnetocaloric (MC) effects and excellent glass forming ability (GFA) have been recognized as promising candidates for magnetic refrigeration (MR). In this work, the RE 60 Co 20 Al 20 (RE = Ho, Er, Tm) amorphous ribbons were successfully fabricated and systematically determined with respect to the GFA, magnetic properties and MC effects. A second order magnetic phase transition (MPT) from ferromagnetic to paramagnetic (FM to PM) without noticeable field or thermal hysteresis has been observed around the Curie temperatures, T C ~ 22.3 K for Ho 60 Co 20 Al 20 , ~ 10.3 K for Er 60 Co 20 Al 20 , and ~ 5.0 K for Tm 60 Co 20 Al 20 , respectively. The MC parameters including the maximum magnetic entropy change (| Δ S M max |), temperature-averaged entropy change with 3 K lift [ TEC (3 K)], and relative cooling powder/refrigerant capacity (RCP/RC) have been determined to check the MC performances, and the corresponding values are determined to be 14.16, 15.57 and 15.06 J/kgK, to be14.04, 15.38 and 14.78 J/kgK, and to be 625.0/478.7, 505.7/391.8 and 334.0/243.4 J/kg for Ho 60 Co 20 Al 20 , Er 60 Co 20 Al 20 and Tm 60 Co 20 Al 20 under the field change Δμ 0 H = 5 T, respectively. The present results indicate that RE 60 Co 20 Al 20 (RE = Ho, Er, Tm) amorphous ribbons are considerable for cryogenic MR application. • The RE 60 Co 20 Al 20 (RE = Ho, Er, Tm) amorphous ribbons are fabricated. • The glass forming ability in RE 60 Co 20 Al 20 amorphous ribbons was investigated. • Large magnetocaloric effect in RE 60 Co 20 Al 20 has been observed. • RE 60 Co 20 Al 20 ribbons are considerable for cryogenic magnetic refrigeration. [ABSTRACT FROM AUTHOR]

We herein provided a systematical determination of the structural and magnetic properties, especially of the magnetocaloric effect (MCE) and magnetocaloric performances of four rare-earth oxychlorides, i. e., the RE OCl (RE = Ho, Dy, Tb and Gd) compounds. The studied RE OCl compounds are all crystallized in the tetragonal matlockite structure (P 4/ nmm space group) and the RE , O, and Cl elements are with the RE 3+, O2−, and Cl− valence states, respectively. The DyOCl, TbOCl and GdOCl compounds reveal an antiferromagnetic transition at around approximate 9.5, 3.7 and 4.8 K, respectively. The magnetocaloric performances are checked by the maximum magnetic entropy change, relative cooling power, and temperature-averaged entropy change with 5 K lift, which are found to be 14.16 J/kgK, 375.55 J/kg and 13.89 J/kgK for HoOCl, to be 14.88 J/kgK, 488.14 J/kg, and 14.60 J/kgK for DyOCl, to be 14.59 J/kgK, 419.67 J/kg, and 14.42 J/kgK for TbOCl, and to be 16.16 J/kgK, 213.68 J/kg, and 14.39 J/kgK for GdOCl, with the magnetic field change of 0–7 T, respectively. [ABSTRACT FROM AUTHOR]

The ternary rare earth RE CoSi 2 (RE = Er and Tm) intermetallic compounds were synthesized by means of arc-melting technique and their crystal structure, magnetism and magneto-caloric effect (MCE) were studied systematically. Both ErCoSi 2 and TmCoSi 2 crystallize in a CeNiSi 2 -type structure (Cmcm space group) confirmed by FULLPROF Rietveld refinement. Magnetization data indicates the antiferromagnetic (AFM) ground state for both RE CoSi 2 compounds, and a magnetic field-induced ferromagnetic (FM) transition occurs below the Neel temperature T N ∼6.9 K for ErCoSi 2 and ∼5.4 K for TmCoSi 2. Considerable reversible MCE in ErCoSi 2 and TmCoSi 2 was observed. The MCE performances of RE CoSi 2 are evaluated by -Δ S M max (maximal magnetic entropy change), TEC (3) (temperature averaged entropy change), and RCP (relative cooling power) with the values of 7.1 J/kg K, 6.8 J/kg K and 165.9 J/kg for ErCoSi 2 , as well as 8.7 J/kg K, 8.5 J/kg K and 152.9 J/kg for TmCoSi 2 , respectively, under Δ H (field change) of 0–50 kOe. Image 1 • CeNiSi 2 -type RE CoSi 2 (RE = Er and Tm) compounds were fabricated. • AFM ordering at T N ∼6.9 K for ErCoSi 2 and ∼5.4 K for TmCoSi 2. • A field-induced AFM to FM transition for both compounds occur below T N. • Considerable values of -Δ S M max, TEC , RC and RCP were found. • RE CoSi 2 compounds are also considerable for cryogenic magnetic cooling. [ABSTRACT FROM AUTHOR]

We herein investigated four rare earth (RE)-based oxides, the RE 2 SiO 5 (RE = Gd, Dy, Ho, and Er) silicates, regarding their structural and cryogenic magnetic properties. All the RE 2 SiO 5 silicates are found to crystallized in a monoclinic structure. X-ray photoemission spectroscopy spectra illustrate that RE , Si and O elements in RE 2 SiO 5 silicates are present as RE 3+, Si4+, and O2−, respectively. The Dy 2 SiO 5 reveals a first-order magnetic transition around 4.5 K. The magnetic phase transition temperatures are probably below 2 K for the RE 2 SiO 5 (RE = Gd, Ho, and Er) silicates. Large cryogenic magnetocaloric effects (MCE) and good magnetocaloric performances were observed in the RE 2 SiO 5 silicates. The MCE parameters in terms of the maximum magnetic entropy changes, the temperature-averaged entropy change (5 K-lift) and refrigerant capacity under a magnetic field change of 0–5 T are determined to be 35.5, 30.4 J/kgK, and 215.7 J/kg for Gd 2 SiO 5 , to be 13.3, 12.9 J/kgK, and 190.5 J/kg for Dy 2 SiO 5 , to be 15.3, 15.1 J/kgK, and 274.1 J/kg for Ho 2 SiO 5 and to be 17.9, 16.5 J/kgK, and 181.14 J/kg for Er 2 SiO 5 , respectively. These derived values of MCE parameters of the RE 2 SiO 5 silicates, especially for Gd 2 SiO 5 , are at similarly high level with or better than those of the updated candidate materials, making them also of potential for practical magnetic refrigeration applications. [ABSTRACT FROM AUTHOR]

The crystal structure, magnetism, and magnetocaloric effect (MCE) were investigated in ternary Er2Ni2Ga compound. The Er2Ni2Ga belongs to W2B2Co-type structure (orthorhombic, space group Immm). The magnetization measurements indicate that Er2Ni2Ga suffers a field-induced metamagnetic transition (antiferromagnetic–ferromagnetic) below Néel temperature (TN) of 7.1 K. Inverse MCE occurs with magnetic field change ($\Delta H$) lower than 0–30 kOe and at low temperatures, whereas normal reversible MCE happens with higher $\Delta \text{H}$. The calculated $-\Delta S_{M}$ (magnetic entropy change) has a peak value of 12.93 J/kg K (~9 K) with refrigerant capacity value of 265 J/kg (5–30 K) for Er2Ni2Ga under $\Delta H$ of 0–70 kOe. [ABSTRACT FROM AUTHOR]

[Display omitted] • The Er 2 BaCu 1- x Ni x O 5 oxides were fabricated. • The structural and magnetic properties were investigated. • Large magnetocaloric effects were observed. • The Er 2 BaCu 1- x Ni x O 5 oxides may considerable for magnetic cooling. The solid-state magnetic cooling based on the magnetocaloric (MC) effects was recognized as one of the most prospective alternative cooling methods to the gas compression technology. Exploring suitable candidate materials with prominent MC performances remains an urgent research priority in this field. Thus, we herein investigated fabricated the Er 2 BaCu 1- x Ni x O 5 oxides (x = 1/3, 1/2, and 2/3) and experimentally determined their structural and magnetic properties together with their MC performances. All the present studied Er 2 BaCu 1- x Ni x O 5 oxides are crystallized in the RE -211 type oxide structure (space group: Pnma). Considerable reversible low-temperature MC effects and good MC performances have been observed in present studied Er 2 BaCu 1- x Ni x O 5 oxides which were assessed by determination the parameters including the magnetic entropy changes, temperature-averaged entropy changes, and relative cooling power. [ABSTRACT FROM AUTHOR]

The crystal structure, microstructure, magnetic phase transitions and magnetocaloric effect (MCE) in KNaSnF6-type GdCrWO 6 and ErCrWO 6 oxides have been investigated. Both GdCrWO 6 and ErCrWO 6 oxides are confirmed to crystalize in a polar aeschynite type structure with the space group of Pna 2 1 (No.33, oP36). The grain size remains relatively average according to the SEM graph. Under low magnetic field of 0.1 T, the ErCrWO 6 oxide undergoes two successive magnetic transitions around 22 and 7 K, whereas only a weak magnetic transition around 6 K can be noticed. The paramagnetic Curie temperatures θ p are fitted to be −17.0 and −16.6 K for GdCrWO 6 and ErCrWO 6 oxides, respectively, suggesting that the antiferromagnetic (AFM) interaction is dominant at ground state. With the magnetic field change (ΔH) of 0–7 T, the peak value of magnetic entropy change (-ΔS M), refrigeration capacity (RC), relative cooling power (RCP) and 5 K lift temperature-averaged ΔS M (TEC) are figured to be 9.13 J/kg-K, 152 J/kg, 190 J/kg and 9.07 J/kg-K for GdCrWO 6 as well as to be 5.3 J/kg-K, 128 J/kg, 161 J/kg and 5.09 J/kg-K for ErCrWO 6 , respectively. The MCE parameters for GdCrWO 6 and ErCrWO 6 oxides are comparable with recently reported RE -based MCE oxides, indicating present GdCrWO 6 and ErCrWO 6 oxides also considerable for cryogenic magnetic refrigeration (MR). [ABSTRACT FROM AUTHOR]

• The RE 2 Ga 2 Mg (RE = Tm, Er, Ho) compounds were fabricated. • The magnetic and magnetocaloric properties were investigated. • Large conventional and inverse magnetocaloric effects were observed. • The Tm 2 Ga 2 Mg is considerable for cryogenic magnetic cooling. The Mo 2 FeB 2 -type compounds RE 2 Ga 2 Mg (RE = Tm, Er, Ho) (space group P 4/ mbm) exhibit a large magnetocaloric (MC) effect which makes them promising for use in cryogenic magnetic cooling applications. They exhibit low temperature metamagnetic nature below their Néel temperatures of 6.8, 11.7 and 18.4 K for Tm 2 Ga 2 Mg, Er 2 Ga 2 Mg and Ho 2 Ga 2 Mg, respectively. The magnetic entropy change, the temperature-averaged entropy change (3 K-lift), and the relative cooling power under a magnetic field change of 0–7 T are 15.6, 15.4 J/kgK and 275.8 J/kg for Tm 2 Ga 2 Mg; 13.2, 13.0 J/kgK and 268.0 J/kg for Er 2 Ga 2 Mg; as well as 9.1, 9.0 J/kgK and 223.0 J/kg for Ho 2 Ga 2 Mg, respectively. [ABSTRACT FROM AUTHOR]

In this work, polycrystalline oxides viz., Ho 2 CrMnO 6 (HCMO) and Er 2 CrMnO 6 (ECMO), were prepared using the sol-gel process, and their crystal structure, magnetic properties, and magnetocaloric effects (MCEs) were studied. X-ray refinement results demonstrate that both oxides exhibited the B -site disordered perovskite type structure (Pbnm space group). A ferromagnetic-paramagnetic phase transition as well as large reversible MCEs was also observed at Curie temperatures (T C) of ~6.1 and ~5.2 K for HCMO and ECMO, respectively. For a magnetic field change (ΔH) of 0–7 T, the maximum magnetic entropy change (-Δ S M), temperature-averaged entropy change (TEC 3), and relative cooling power (RCP) were estimated to be 11.03 J/kgK, 11.02 J/kgK, and 322.7 J/kg for HCMO, and 12.94 J/kgK, 12.80 J/kgK and 277.5 J/kg for ECMO. [ABSTRACT FROM AUTHOR]

The magnetic refrigeration (MR) by utilizing the magnetocaloric effect (MCE) of magnetic solids has been considered a promising, environmentally benign, energy-efficient cooling technology. However, the lack of promising magnetic substances has slowed the development of its active application. To identify suitable candidate materials, we herein identified the structural and magnetic properties together with the MCE and magnetocaloric performances of rare earth (RE) rich RE 6 Ni 2.25 Al 0.75 (RE = Dy, Ho and Er) compounds. All the RE 6 Ni 2.25 Al 0.75 compounds are confirmed to crystallized in orthogonal Ho 6 Co 2 Ga-type structure and underwent paramagnetic to antiferromagnetic magnetic transitions. Moreover, large direct (conventional) and inverse MCEs have been observed in all the RE 6 Ni 2.25 Al 0.75 compounds. The values of peak magnetic entropy changes, temperature-averaged magnetic entropy changes with 5 K-lift and relative cooling powers under magnetic field change of 0–7 T are evaluated to be − 4.44 J/kg-K, − 4.38 J/kg-K and 230.6 J/kg for Dy 6 Ni 2.25 Al 0.75 , to be − 12.68 J/kg-K, − 12.26 J/kg-K and 378.2 J/kg for Ho 6 Ni 2.25 Al 0.75 , and to be − 17.52 J/kg-K, − 17.33 J/kg-K and 465.7 J/kg for Er 6 Ni 2.25 Al 0.75 , respectively. • The RE6Ni2.25Al0.75 (RE = Dy, Ho and Er) compounds are fabricated. • The structural and magnetic properties were investigated. • Large direct and inverse magnetocaloric effects were observed. • The Er6Ni2.25Al0.75 is considerable for cryogenic magnetic refrigeration. [ABSTRACT FROM AUTHOR]

The glass forming ability, magnetism and magneto-caloric effect have been investigated in Er 60 Ni 30 Co 10 melt-spun alloy by using X-ray diffraction, differential scanning calorimetry and magnetization measurements. The amorphousized Er 60 Ni 30 Co 10 exhibits a relatively wide supercooled liquid region of 40 K and a second-order ferromagnetic transition around Curie temperature of 11.5 K. Under Δ Η (magnetic field change) of 0–5 T, the values of −Δ S M max (maximum magnetic entropy change) and RCP (relative cooling power) are 12.1 J/kg K and 342 J/kg, respectively. Furthermore, the field dependence of the magnetic entropy change for Er 60 Ni 30 Co 10 obeys the phenomenological universal curve and corresponds to a field independent exponent of n  = 0.58 ± 0.03. [ABSTRACT FROM AUTHOR]

Rare earth (RE) based RE - TM - X (TM = transition metal elements; X = P - block elements) materials have received continuous attention due to the exhibition of various intriguing magnetic functional characteristics. In this work, a combined experimental and theoretical investigation has been conducted in detail for RE Co 12 B 6 (RE = Ce, Pr, Nd) compounds with regard to their structural and magnetic properties, particularly the magnetocaloric effect and magnetic phase transition (MPT). All of the present RE Co 12 B 6 compounds are found to crystalize in the SrNi 12 B 6 -type structure and with a ferrimagnetic ground state, which is confirmed by density functional theory calculations and magnetization measurements. The magnetic moments of RE atoms and Co atoms tend to be in antiparallel alignment, and the MPT of these materials originates primarily from the spin-polarized 3 d electrons of the Co atoms, which can be greatly affected by the 4 f electrons of RE atoms. Considerable magnetocaloric effects have been observed around its own T C of 130, 157, and 160 K, for CeCo 12 B 6 , PrCo 12 B 6 , and NdCo 12 B 6 , respectively, which is related to a typical second-order MPT. The corresponding maximum magnetic entropy change and relative cooling power values,with field changes of 0–70 kOe, are determined to be 2.54, 2.84, and 2.77 J/kg K and 116.8, 156.2, and 155.1 J/kg, respectively. The MPT properties of present RE Co 12 B 6 compounds were studied in further detail by critical analysis using the modified Arrott Plot and Kouvel-Fisher methods, which can be explained within the frame of the 3D Heisenberg model with short-range magnetic interaction. [Display omitted] [ABSTRACT FROM AUTHOR]

The magnetic properties and magnetocaloric effect (MCE) in dysprosium zinc binary DyZn compound were studied. The compound reveals a paramagnetic-to-ferromagnetic transition together with a spin reorientation phenomenon at Curie temperatures of T C ∼135 and T SR ∼50 K, respectively. A large reversible MCE was observed in DyZn around T C . For the magnetic field change of 0–7 T, the values of maximum magnetic entropy change (–Δ S M max ), relative cooling power ( RCP ), and refrigerant capacity ( RC ) were 12.2 J/kg K, 895 J/kg, and 672 J/kg, respectively. [ABSTRACT FROM AUTHOR]

The structural, magnetic, and magnetocaloric properties of Ni 44 Mn 45-x Sn 11 Fe x (x = 0, 1, 2 and 3) Heusler alloys have been studied detailly by means of X-ray diffraction, differential scanning calorimetry, and magnetization measurements. The martensitic transition temperature (T M) and austenite Curie temperature (T A C) increase gradually with increasing Fe content. Large differences in magnetization between the ferromagnetic austenite and weakly magnetic martensite phases and obvious thermal hysteresis have also been observed during the martensite transformation. With the magnetic field change up to 0–7 T, the maximum value of magnetic entropy changes reaches 26.7 and 23 J kg−1K−1 for x = 1 and 2, respectively, which are much larger than the undoped sample (9.8 J kg−1K−1). Whereas, the effective refrigerant capacity RC eff reduced due to Fe doping increased the hysteresis loss. The alloy for x = 1 has highest RC value of 172 (255) J kg−1 for a magnetic field change of 0–5 T (0–7 T), furthermore, a large magnetic entropy change and moderate RC eff has been obtained around room temperature. • Fe-doped Ni44Mn45-xSn11Fex (x = 0, 1, 2 and 3) Heusler alloys were fabricated. • Structural and magnetic properties of Ni44Mn45-xSn11Fex were investigated. • Considerable magnetocaloric performances in Ni44Mn44Sn11Fe were realized. [ABSTRACT FROM AUTHOR]

• The magnetism and magnetocaloric effect (MCE) were investigated in Er 4 CoCd compound. • A large magnetocaloric effect in Er 4 CoCd compound was observed. • The origin of MCE and its potential application in Er 4 CoCd were discussed. The Er-based compound Er 4 CoCd was synthesized successfully and its structural, magnetic together with magnetocaloric properties were investigated in detail. The Er 4 CoCd crystallized in a Gd 4 RhIn-type structure with the space group of F 4 ¯ 3 m , which was confirmed by Rietveld refinement. A ferromagnetic transition was observed around its Curie temperature (T C) of 12.5 K accompanied by a large magnetocaloric effect (MCE). The performance of MCE for Er 4 CoCd was evaluated by the isothermal maximal magnetic entropy (- Δ S M max) , the temperature averaged entropy change (TEC) at 10 K temperature lift [ TEC (10 K)], and the relative cooling power (RCP). The values of - Δ S M max , TEC (10 K), and RCP of Er 4 CoCd are 20.4 J/kg K, 19.2 J/kg K, and 503 J/kg under the magnetic field change (Δ H) of 0–5 T, respectively. [ABSTRACT FROM AUTHOR]