Multiferroicity in an organic charge-transfer salt that is suggestive of electric-dipole-driven magnetism
- Materials Science Division
Multiferroics, showing simultaneous ordering of electrical and magnetic degrees of freedom, are remarkable materials as seen from both the academic and technological points of view. A prominent mechanism of multiferroicity is the spin-driven ferroelectricity, often found in frustrated antiferromagnets with helical spin order. There, as for conventional ferroelectrics, the electrical dipoles arise from an off-centre displacement of ions. However, recently a different mechanism, namely purely electronic ferroelectricity, where charge order breaks inversion symmetry, has attracted considerable interest. Here we provide evidence for ferroelectricity, accompanied by antiferromagnetic spin order, in a two-dimensional organic charge-transfer salt, thus representing a new class of multiferroics. We propose a charge-order-driven mechanism leading to electronic ferroelectricity in this material. Quite unexpectedly for electronic ferroelectrics, dipolar and spin order arise nearly simultaneously. This can be ascribed to the loss of spin frustration induced by the ferroelectric ordering. Hence, here the spin order is driven by the ferroelectricity, in marked contrast to the spin-driven ferroelectricity in helical magnets.
- Research Organization:
- Argonne National Laboratory (ANL)
- Sponsoring Organization:
- SC
- DOE Contract Number:
- AC02-06CH11357
- OSTI ID:
- 1050812
- Report Number(s):
- ANL/MSD/JA-72070
- Journal Information:
- Nature Materials, Journal Name: Nature Materials Journal Issue: 9 Vol. 11; ISSN 1476-1122
- Country of Publication:
- United States
- Language:
- ENGLISH
Similar Records
Evidence for a single-layer van der Waals multiferroic
Electric modulation of conduction in multiferroic Ca-doped BiFeO3 films