Počet záznamů: 1  

Chemical and physical pressure effects in the A-site spinel antiferromagnets CoM.sub.2./sub.O.sub.4./sub. (M = Al, Co, and Rh)

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    0538257 - FZÚ 2021 RIV GB eng J - Článek v odborném periodiku
    Naka, T. - Valenta, J. - Kaštil, Jiří - Míšek, Martin - Prchal, J. - Sechovský, V. - Abe, H. - Nakane, T. - Nakayama, M. - Uchikoshi, T.
    Chemical and physical pressure effects in the A-site spinel antiferromagnets CoM2O4 (M = Al, Co, and Rh).
    Materials Research Express. Roč. 7, č. 5 (2020), s. 1-14, č. článku 056105. E-ISSN 2053-1591
    Grant CEP: GA MŠMT(CZ) LM2018096
    Institucionální podpora: RVO:68378271
    Klíčová slova: magnetic transition * pressure effects * diamond lattice * antiferromagnetism * magnetic frustration
    Obor OECD: Condensed matter physics (including formerly solid state physics, supercond.)
    Impakt faktor: 1.620, rok: 2020
    Způsob publikování: Open access

    Magnetic phase transitions under high pressure are reported for the diamond lattice antiferromagnet Co3-xRhxO4 in the range of 0 <= x <= 2.0, which is an isostructural S = 3/2 system for the well-known frustrated antiferromagnet CoAl2O4. In the Co3-xRhxO4 system, magnetic and specific-heat measurements at ambient pressure revealed that a second-order antiferromagnetic transition occurred at the Neel temperature (T-N) which exhibits a nonmonotonic x-variation. The physical pressure variations of T-N were determined by ac-calorimetry under hydrostatic pressures up to p = 2.6 GPa for Co2RhO4 and CoRh2O4. The rates of change of T-N with pressure (i.e., the pressure coefficients), 1.93 and 1.61 K GPa(-1), respectively, were comparable to those for CoAl2O4 and Co3O4, respectively. The pressure coefficients of magnetic ordering temperature for these A-site spinel compounds were considerably larger than those for other spinel and iron-garnet compounds which follow the empirical '10/3 law'. Simple analysis of the chemical and physical pressure coefficients of T-N revealed that T-N depended on both the lattice volume and the oxygen positional parameter u.
    Trvalý link: http://hdl.handle.net/11104/0316096

     
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