Competing rhombohedral and monoclinic crystal structures in MnPn2Ch4 compounds: An ab-initio study

• Published in: Journal of alloys and compounds Vol. 709; pp. 172 - 178
• Main Authors: Eremeev, S.V., Otrokov, M.M., Chulkov, E.V.
• Format: Journal Article
• Language: English
• Published: Lausanne Elsevier B.V 30.06.2017; Elsevier BV
• Subjects: Antiferromagnetism; Antimony; Atomic structure; Bonding strength; Coupling; Crystal structure; Density; Density functional theory; Electron spin; Ferromagnetism; Interlayers; Magnetic ordering; Magnetic properties; Magnetism; Theory; Magnetic ordering; Density functional theory; Crystal structure
• ISSN: 0925-8388; 1873-4669
• DOI: 10.1016/j.jallcom.2017.03.121

Based on the relativistic spin-polarized density functional theory calculations we investigate the crystal structure, electronic and magnetic properties of a family MnPn2Ch4 compounds, where pnictogen metal atoms (Pn) are Sb and Bi; chalcogens (Ch) are Se, Te. We show that in the series the compounds of this family with heavier elements prefer to adopt rhombohedral crystal structure composed of weakly bonded septuple monoatomic layers while those with lighter elements tend to be in the monoclinic structure. Irrespective of the crystal structure all compounds of the MnPn2Ch4 series demonstrate a weak energy gain (of a few meV per formula unit or even smaller than meV) for antiferromagnetic (AFM) coupling for magnetic moments on Mn atoms with respect to their ferromagnetic (FM) state. For rhombohedral structures the interlayer AFM coupling is preferable while in monoclinic phases intralayer AFM configuration with ferromagnetic ordering along the Mn chain and antiferromagnetic ordering between the chains has a minimum energy. Over the series the monoclinic compounds are characterized by substantially wider bandgap than compounds with rhombohedral structure. •DFT calculations show the structure of MnPn2Ch4 compounds depends on composition.•Irrespective of the structure all compounds demonstrate antiferromagnetic ordering.•The type of crystal structure significantly influences the bandgap width.