Field induced metamagnetism and large magnetic entropy change in RRhSi (R = Tb, Dy, Ho) rare earth intermetallics

被引:4
|
作者
Gupta, S. [1 ,2 ]
Lukoyanov, A. V. [3 ,4 ,5 ]
Knyazev, Yu. V. [3 ]
Kuz'min, Yu. I. [3 ]
Suresh, K. G. [2 ]
机构
[1] Univ Leeds, Leeds LS2 9JT, W Yorkshire, England
[2] Indian Inst Technol, Dept Phys, Mumbai 400076, Maharashtra, India
[3] Russian Acad Sci, MN Miheev Inst Met Phys, Ural Branch, Ekaterinburg 620108, Russia
[4] Ural Fed Univ, Ekaterinburg 620002, Russia
[5] Skolkovo Inst Sci & Technol, Moscow 121205, Russia
基金
俄罗斯科学基金会;
关键词
Rare-earth intermetallics; Large magnetocaloric effect; Magnetic properties; Electronic structure; Optical properties; ELECTRONIC-STRUCTURE; OPTICAL-PROPERTIES; PHASE-TRANSITIONS; CRYSTAL-STRUCTURE; TBRHSI; ER;
D O I
10.1016/j.jallcom.2021.161493
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report magnetic, magneto-caloric, electronic structure, and optical properties of rare earth intermetallics RRhSi (R=Tb, Dy, Ho). These compounds show antiferromagnetic ordering at low temperatures. The magnetization data reveal field-induced metamagnetic transition in DyRhSi and HoRhSi compounds, which results in large magnetocaloric effect (MCE) in these compounds. In the case of Dy, the MCE is found to be larger than those of other analogs of the RTX family. Theoretical calculations confirm anti ferromagnetic ordering in these compounds and show a negligible contribution of magnetic moment from Rh atom. The optical measurements carried out for these materials support the theoretical calculations. We uncover large magnetocaloric effect in DyRhSi and HoRhSi intermetallics attributed to metamagnetic transition and identify electronic states involved in the formation of magnetic and spectral properties based on DFT+U and optical studies. (c) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页数:6
相关论文
共 50 条
  • [41] Metamagnetism and giant magnetoresistance of the rare-earth intermetallic compounds R2Ni2Pb (R=Er,Ho,Dy) -: art. no. 020409
    Chinchure, AD
    Sandoval, EM
    Mydosh, JA
    PHYSICAL REVIEW B, 2002, 66 (02): : 1 - 4
  • [43] Neutron Larmor diffraction investigation of the rare-earth pyrochlores R2Ti2O7 (R = Tb, Dy, Ho)
    Ruminy, M.
    Groitl, F.
    Keller, T.
    Fennell, T.
    PHYSICAL REVIEW B, 2016, 94 (17)
  • [44] ANISOTROPIC MAGNETIC-SUSCEPTIBILITY AND CRYSTAL-FIELD EFFECT OF RZN(2) (R=TB, DY, HO AND ER)
    KITAI, T
    JOURNAL OF THE PHYSICAL SOCIETY OF JAPAN, 1995, 64 (09) : 3403 - 3408
  • [45] Raman scattering studies of hexagonal rare-earth RMnO3 (R = Tb, Dy, Ho, Er) thin films
    Nguyen Thi Minh Hien
    Oh, Su-Young
    Chen, Xiang-Bai
    Lee, D.
    Jang, S. -Y.
    Noh, T. W.
    Yang, In-Sang
    JOURNAL OF RAMAN SPECTROSCOPY, 2011, 42 (09) : 1774 - 1779
  • [46] REFINEMENT OF CRYSTAL-STRUCTURE OF SOME RARE-EARTH VANADATES RVO4 (R=DY, TB, HO, YB)
    FUESS, H
    KALLEL, A
    JOURNAL OF SOLID STATE CHEMISTRY, 1972, 5 (01) : 11 - &
  • [47] Magnetic hyperfine interactions on Cd sites of the rare-earth cadmium compounds RCd (R=Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, and Er)
    Cavalcante, F. H. M.
    Leite Neto, O. F. L. S.
    Saitovitch, H.
    Cavalcante, J. T. P. D.
    Carbonari, A. W.
    Saxena, R. N.
    Bosch-Santos, B.
    Pereira, L. F. D.
    Mestnik-Filho, J.
    Forker, M.
    PHYSICAL REVIEW B, 2016, 94 (06)
  • [48] Ab Initio Magnetic Properties Simulation of Nanoparticles Based on Rare Earth Trifluorides REF3 (RE = Tb, Dy, Ho)
    Saidakhmetov, Pulat
    Piyanzina, Irina
    Faskhutdinova, Amina
    Nedopekin, Oleg
    Adyrbekova, Gulmira
    Baiman, Gulzagira
    Suyerkulova, Zhamilya
    Romanova, Irina
    CRYSTALS, 2023, 13 (10)
  • [49] Magnetic properties of heavy rare-earth metallofullerenes M@C82 (M = Gd, Tb, Dy, Ho, and Er)
    Huang, HJ
    Yang, SH
    Zhang, XX
    JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (07): : 1473 - 1482
  • [50] MAGNETIC-STRUCTURES OF THE RARE-EARTH ORTHOTITANITES RTIO3 R=TB,DY,TM AND YB
    TURNER, CW
    COLLINS, MF
    GREEDAN, JE
    JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS, 1981, 23 (03) : 265 - 273