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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]

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]

We herein fabricated two gadolinium-transition metal-based high entropy (HE) oxides of Gd(Mn 0.25 Fe 0.25 Al 0.25 Cr 0.25)O 3 [denoted as Gd(4 TM 0.25)O 3 ] and Gd(Mn 0.2 Fe 0.2 Al 0.2 Co 0.2 Ni 0.2)O 3 [denoted as Gd(5 TM 0.2)O 3 ] and determined their structural, magnetic, and magnetocaloric properties. Both of present HE oxides are found to crystallize in the single-phase perovskite-type orthorhombic structure with a homogeneous microstructure and exhibit prominent cryogenic magnetocaloric performances. The values of magnetic entropy change, refrigerant capacity, and temperature-averaged entropy change (6K-lift) under the magnetic field change of 0–7 T are estimated to be 20.34 J/kgK, 295.4 J/kg, and 19.56 J/kgK for Gd(4 TM 0.25)O 3 , and to be 22.45 J/kgK, 258.2 J/kg, and 20.79 J/kgK for Gd(5 TM 0.2)O 3 , respectively, which are comparable with recently reported candidate materials for practical magnetic cooling. These findings not only indicate potential applications of present perovskite-type Gd(4 TM 0.25)O 3 and Gd(5 TM 0.2)O 3 HE oxides, but also provide meaningful clues for exploring HE oxides with prominent cryogenic magnetocaloric performances. [ABSTRACT FROM AUTHOR]

We herein fabricated the (Dy 0.25 Ho 0.25 Er 0.25 Tm 0.25) 2 Cu 2 In high-entropy (HE) compounds and systematically determined its structural, magnetic, and magnetocaloric properties. The (Dy 0.25 Ho 0.25 Er 0.25 Tm 0.25) 2 Cu 2 In HE compound was found to crystalize in a tetragonal Mo 2 B 2 Fe type structure (P4/ mbm space group) and undergoes typical second order type magnetic transition. Large MCE and prominent cryogenic magnetocaloric performances were observed in (Dy 0.25 Ho 0.25 Er 0.25 Tm 0.25) 2 Cu 2 In HE compound. The evaluated values of magnetic entropy change and refrigerant capacity of (Dy 0.25 Ho 0.25 Er 0.25 Tm 0.25) 2 Cu 2 In HE compound under magnetic field change of 0–7 T are 17.1 J/kgK and 398.0 J/kg which are comparable with the reported candidate materials for cryogenic magnetic cooling, making the present (Dy 0.25 Ho 0.25 Er 0.25 Tm 0.25) 2 Cu 2 In HE compound also considerable for practical applications. • The (Dy 0.25 Ho 0.25 Er 0.25 Tm 0.25) 2 Cu 2 In HE compound was fabricated. • The structural, magnetic, MPT and MC properties were investigated. • The present HE compound is considerable for cryogenic magnetic cooling. [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 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 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]