Natural ferroelectric order near ambient temperature in HoFeO3: A member of RFeO3 orthoferrites
arXiv:1909.05002 · doi:10.1103/PhysRevB.100.214432
Abstract
Current scenario in multiferroics demands a breakthrough discovery of promising materials after BiFeO3. Recently, the controversial discovery of room temperature ferroelectricity (FE) in SmFeO3 [PRL 107, 117201 (2011); 113, 217203 (2014)] inspires the investigation of HoFeO3. Here, we report a natural ferroelectric order below 210 K (TFE) along c-axis with reasonably large polarization and low-field strong magnetoelectric coupling. Synchrotron and neutron diffraction results confirm that a shift of O atoms along c-axis of polar Pbn21 structure causes FE in HoFeO3. The exchange striction mechanism is suggested to elucidate the ferroelectric order. The results create a renewed attention for searching promising candidates with a natural ferroelectric order and higher TFE in the rest of the RFeO3 series.
References in corpus (7)
- k=0 magnetic structure and absence of ferroelectricity in SmFeO3
- Magnetic phase transitions and magnetoelectric coupling of GdFeO_3 single crystals probed by low-temperature heat transport
- Local inversion symmetry breaking and spin-phonon coupling in perovskite GdCrO3
- Exchange striction induced giant ferroelectric polarization in copper based multiferroic material -CuVO
- Non-resonant and Resonant X-ray Scattering Studies on Multiferroic TbMn2O5
- High-temperature ferroelectric order and magnetic field-cooled effect driven magnetoelectric coupling in R2BaCuO5 (R= Er, Dy, Sm)
- Single crystal polarized neutron diffraction study of the magnetic structure of HoFeO