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Abstract Magnetic cooling technology based on the magneto-caloric effect (MCE) has emerged as a viable alternative to conventional vapor compression refrigeration technology. Exploring suitable magnetic solids with promising magneto-caloric performances is a key issue in this field. Here, we report a systematic characterization of the glass forming ability, microstructure, magnetism and MCE of Ho 57 Cu 25 Al 18 and Tm 57 Cu 25 Al 18 amorphous ribbons. Promising MCE performances were observed for both ribbons at low temperature. Compared with most of the rare earth-based amorphous alloys, both ribbons were found to have comparable or even larger values of -Δ S M max (maximum magnetic entropy change), RC (refrigeration capacity) and RCP (relative cooling power). These promising magneto-caloric performances make amorphousized RE 57 Cu 25 Al 18 ribbons attractive for active cryogenic magnetic refrigeration. Highlights • Magnetism and magnetocaloric effect (MCE) in RE 57 Cu 25 Al 18 ribbons were studied. • Promising MCE performance was observed in amorphous RE 57 Cu 25 Al 18 ribbons. • The origin of MCE in amorphous RE 57 Cu 25 Al 18 ribbons was 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]

Pyrochlore RE 2 TiMnO 7 ( RE = Dy and Ho) compounds were synthesized using a ceramic method, and their crystal structures, microstructures, and cryogenic magnetic properties were determined. Dy 2 TiMnO 7 and Ho 2 TiMnO 7 compounds belong to the Fd-3m space group with a cubic pyrochlore structure and show a considerable reversible magnetocaloric effect (MCE) in the vicinity of the second-order ferromagnetic-paramagnetic (FM-PM) phase transition at the Curie temperature ( T C ) of 7.6 and 7.5 K, respectively. The obtained maximal values of magnetic entropy change (-Δ S M max ) for Dy 2 TiMnO 7 and Ho 2 TiMnO 7 are 12.50 and 13.95 J/kg K under a magnetic field change (Δ H ) of 0–7 T, respectively. Correspondingly, the relative cooling power ( RCP ) values reach 530.3 and 573.2 J/kg, respectively. [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]

The magnetic properties and magnetic entropy change of amorphousized Tm 60 Co 20 Ni 20 ribbon were systematically studied. The results indicate that the Tm 60 Co 20 Ni 20 amorphous ribbon reveals a second order magnetic transition (paramagnetic to ferromagnetic state) based on the Arrott plots and rescaled magnetic entropy change curves. A large magnetic entropy change is achieved around its Curie temperature of T C ∼6.7 K. Under the magnetic field change (Δ Η ) of 0–5 T, the maximum values of magnetic entropy change (−Δ S M max ) and relative cooling power ( RCP ) are 17.1 J/kg K and 273 J/kg, respectively. In particular, under a relative low Δ Η of 0–2 T, a large magnetic entropy change of 11.8 J/kg K reaches, making it attractive in the field of low-temperature magnetic refrigeration. [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]

We present a detailed investigation of the crystal structure, magnetism and magneto-caloric performances of RE Co 2 B 2 C (RE = Gd, Tb and Dy) compounds. All compounds are described with a LuNi 2 B 2 C-type crystallographic structure (I 4/ mmm space group). A second-ordered paramagnetic to ferromagnetic (PM-FM) transition is observed in RE Co 2 B 2 C compounds around their Curie temperatures (T C) of 17.2, 5.3 and 7.7 K, and induced a considerable magneto-caloric effect (MCE) for GdCo 2 B 2 C, TbCo 2 B 2 C and DyCo 2 B 2 C, respectively. The magneto-caloric performances for RE Co 2 B 2 C were characterized by the isothermal magnetic entropy (- Δ S M max) , temperature averaged entropy change (TEC) with three different temperature lifts (3, 5 and 10 K), and relative cooling power (RCP). The corresponding values of - Δ S M max , TEC (3 K) and RCP under the magnetic field change (Δ H) of 0–5 T, are 10.34 J/kg-K, 10.23 J/kg-K, and 238.1 J/kg for GdCo 2 B 2 C, 18.09 J/kg-K, 17.83 J/kg-K, and 438.2 J/kg for TbCo 2 B 2 C, as well as 17.79 J/kg-K, 17.72 J/kg-K, and 480.1 J/kg for DyCo 2 B 2 C, respectively. • Magnetic properties and MCE in RE Co 2 B 2 C compounds were studied. • Large values of -ΔS M max, TEC, RC and RCP were observed at low temperature. • RE Co 2 B 2 C compounds are competitive for cryogenic magnetic cooling. [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]

In this paper, we reported on the magnetic properties and magneto-caloric effect (MCE) of the aluminium compounds Dy 2 CuAl 3 and Tm 2 CuAl 3 based on the magnetization and isothermal magnetization of various temperature measurements. Both compounds obey magnetic phase transition from a paramagnetic (PM) to ferromagnetic (FM) state (second order) around the Curie temperatures of T C  ∼ 24.5 and 4.7 K together with a considerable reversible MCE for Dy 2 CuAl 3 and Tm 2 CuAl 3 , respectively. The magnetic entropy change (-Δ S M ) and the relative cooling power ( RCP ) were estimated and discussed in terms of MCE. Maximum values of -Δ S M are 6.68 and 11.33 J/kg K for Dy 2 CuAl 3 and Tm 2 CuAl 3 , respectively, for a change in field of 0–5 T. Correspondingly, the values of RCP are 364 J/kg and 216 J/kg. [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]