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Register a new userMagnetic and transport anomalies in R2RhSi3 (R= Gd, Tb, and Dy), resembling those of an exotic magnetic skyrmion Gd2PdSi3
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E. V. Sampathkumaran Professor
Publication date
2020
fields
Physics
and research's language is
English
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We have carried out magnetization, heat capacity, electrical and magnetoresistance measurements (2-300 K) for the polycrystalline form of intermetallic compounds, R2RhSi3 (R= Gd, Tb, and Dy), forming in a AlB2 derived hexagonal structure with a triangular R network. This work was primarily motivated by a revival of interest on Gd2PdSi3 after about two decades in the field of Toplogical Hall Effect due to magnetic skyrmions. We report here that these compounds are characterized by double antiferromagnetic transitions (T_N= 13.5 and 12 K for Gd, 13.5 and 6.5 K for Tb; 6.5 and 2.5 for Dy), but antiferromagnerism seems to be complex. The most notable observations common to all these compounds are: (i) There are many features in the data mimicking those seen for Gd2PdSi3, including the two field-induced changes in isothermal magnetization as though there are two metamagnetic transitions well below T_N. In view of such a resemblance of the properties, we speculate that these Rh-based materials offer a good playground to study toplogical Hall effect in a centrosymmetric structure, with its origin lying in triangular lattice of magnetic R ions; (ii) There is an increasing contribution of electronic scattering with decreasing temperature towards T_N in all cases, similar to Gd2PdSi3, thereby serving as examples for a theoretical prediction for a classical spin-liquid phase in metallic systems due to geometrical frustration.
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We investigated the electronic structure of multiferroic hexagonal RMnO3 (R = Gd, Tb, Dy, and Ho) thin films using both optical spectroscopy and first-principles calculations. Using artificially stabilized hexagonal RMnO3, we extended the optical spectroscopic studies on the hexagonal multiferroic manganite system. We observed two optical transitions located near 1.7 eV and 2.3 eV, in addition to the predominant absorption above 5 eV. With the help of first-principles calculations, we attribute the low-lying optical absorption peaks to inter-site transitions from the oxygen states hybridized strongly with different Mn orbital symmetries to the Mn 3d3z2-r2 state. As the ionic radius of the rare earth ion increased, the lowest peak showed a systematic increase in its peak position. We explained this systematic change in terms of a flattening of the MnO5 triangular bipyramid.
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