Begunovich Lyudmila V, Korshunov Maxim M, Ovchinnikov Sergey G
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, 660036 Krasnoyarsk, Russia.
Siberian Federal University, Svobodny Prospect 79, 660041 Krasnoyarsk, Russia.
Materials (Basel). 2022 Jun 29;15(13):4583. doi: 10.3390/ma15134583.
Electronic structure and magnetic properties of Fe3Se4 are calculated using the density functional approach. Due to the metallic properties, magnetic moments of the iron atoms in two nonequivalent positions in the unit cell are different from ionic values for Fe3+ and Fe2+ and are equal to M1=2.071μB and M2=-2.042μB, making the system ferrimagnetic. The total magnetic moment for the unit cell is 2.135μB. Under isotropic compression, the total magnetic moment decreases non-monotonically and correlates with the non-monotonic dependence of the density of states at the Fermi level N(EF). For 7% compression, the magnetic order changes from the ferrimagnetic to the ferromagnetic. At 14% compression, the magnetic order disappears and the total magnetic moment becomes zero, leaving the system in a paramagnetic state. This compression corresponds to the pressure of 114 GPa. The magnetic ordering changes faster upon application of an isotropic external pressure due to the sizeable anisotropy of the chemical bondings in Fe3Se4. The ferrimagnetic and paramagnetic states occur under pressures of 5.0 and 8.0 GPa, respectively. The system remains in the metallic state for all values of compression.
采用密度泛函方法计算了Fe3Se4的电子结构和磁性。由于其金属特性,晶胞中两个不等价位置的铁原子的磁矩不同于Fe3+和Fe2+的离子值,分别为M1 = 2.071μB和M2 = -2.042μB,使该体系呈现亚铁磁性。晶胞的总磁矩为2.135μB。在各向同性压缩下,总磁矩非单调减小,且与费米能级处的态密度N(EF)的非单调依赖关系相关。对于7%的压缩率,磁序从亚铁磁性转变为铁磁性。在14%的压缩率下,磁序消失,总磁矩变为零,体系处于顺磁状态。这种压缩对应于114 GPa的压力。由于Fe3Se4中化学键的显著各向异性,施加各向同性外部压力时磁序变化更快。亚铁磁性和顺磁状态分别出现在5.0 GPa和8.0 GPa的压力下。对于所有压缩值,该体系均保持金属态。