Spin-gap opening accompanied by a strong magnetoelastic response in the S=1 magnetic dimer system Ba3BiRu2O9
arXiv:1112.0420 · doi:10.1103/PhysRevB.84.220406
Abstract
Neutron diffraction, magnetization, resistivity, and heat capacity measurements on the 6H-perovskite Ba3BiRu2O9 reveal simultaneous magnetic and structural dimerization driven by strong magnetoelastic coupling. An isostructural but strongly displacive first-order transition on cooling through T*=176 K is associated with a change in the nature of direct Ru-Ru bonds within Ru2O9 face-sharing octahedra. Above T*, Ba3BiRu2O9 is an S=1 magnetic dimer system with intradimer exchange interactions J0/kB=320 K and interdimer exchange interactions J'/kB=-160 K. Below T*, a spin-gapped state emerges with Δ\approx220 K. Ab initio calculations confirm antiferromagnetic exchange within dimers, but the transition is not accompanied by long range-magnetic order.
5 pages, 5 figures, accepted by Physical Review B
References in corpus (2)
Cited by in corpus (6)
- Hexagonal Perovskites as Quantum Materials
- Magnetodielectric coupling in a Ru-based 6H-perovskite, Ba3NdRu2O9
- A Spin Glass State in Ba3TiRu2O9
- X-ray crystal structure analysis and the Ru valence of Ba4Ru3O10 single crystals
- Cooperative Ru(4d)-Ho(4f) magnetic orderings and phase coexistence in the 6H-perovskite multiferroic Ba3HoRu2O9
- Unconventional S-orbital state of Tb and cooperative Ru(4d)-Tb(4f) spin-ordering in strongly correlated 4d-4f system, Ba3TbRu2O9