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Magnetism tuning in non-centrosymmetric chiral semiconductor CeRhC2

Subject Area Solid State and Surface Chemistry, Material Synthesis
Term from 2021 to 2024
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 467257848
 
Final Report Year 2025

Final Report Abstract

RRhC2 (R = La, Ce) semiconductors are the only rare-earth transition-metal dicarbides with a chiral crystal structure (space groups P41/P43). The project was focused on the determination of the structural and physical properties of these compounds at the enantiomorph resolution scale and on the study of the response of the magnetic properties of the Ce-based compound upon targeted iso- and non-isoelectronic substitutions in the R- (by La) and T- (by Co, Ir, Ru and Pd) sites. Anisotropy and handedness effects on the electrical transport, especially in the presence of a magnetic field, were of particular interest – beside the basic features - due to possible practically important properties. The combination of precise preparation, careful characterisation of the synthesised materials (in particular using state of the art metallographic techniques) with the fabrication of microdevices by focused ion beam technique is the unique feature of this project and bodes well for its originality. For the first time, EBSD-based precharacterisation of the sample material confirmed both enantiomorphs for LaRhC2, in full agreement with the results of single crystal X-ray structure determination. The semiconducting properties and anisotropy derived from electronic structure calculations are verified by electrical resistivity measurements on single crystalline enantiopure and crystallographically oriented microdevices. In contrast to semiconducting LaRhC2, CeRhC2 exhibits Kondo semimetal properties due to the smaller energy gap. The Ce-containing material showed properties derived from the localised nature of its 4f electronic state. For the first time, the TN of CeRhC2 was found to be independent of crystallographic direction and crystal handedness. Systematic studies of substitutions on the metals sites revealed either a complete suppression of the AFM ordering (Ce by La at x > ~0.5) or a significant decrease of the TN (in particular by substitution of Rh by T = Ru, Pd).

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