Z2 Vortex Crystal Candidate in the Triangular S=1/2 Quantum Antiferromagnet
Abstract
The prospect of merging the paradigms of geometric frustration on a triangular lattice and bond anisotropies in the strong spin-orbit coupling limit holds tremendous promise in the ongoing hunt for exotic quantum materials. Here we identify a new candidate system to realize such physics, the organic quantum antiferromagnet (CD3ND3)2NaRuCl6. We report a combination of thermodynamic, magneto-elastic and neutron scattering experiments on single-crystals to determine the phase diagram in axial magnetic fields H c and propose a minimal model Hamiltonian. (CD3ND3)2NaRuCl6 displays an ideal triangular arrangement of Ru3+ ions adopting the spin-orbital entangled j eff = 1/2 state. It hosts residual magnetic order below T N = 0.23 K and a highly unusual H-T phase diagram including three different incommensurate states. Spin-waves in the high-field polarized regime are well described by a Heisenberg-like triangular lattice Hamiltonian with a potential sub-leading bond dependent anisotropy term J. We discuss possible candidate magnetic structures in the various observed phases and propose two mechanisms that could explain the field-dependent incommensurability, requiring either a small ferromagnetic Kitaev term or a tiny magneto-elastic J-J' isosceles distortion driven by pseudospin-lattice coupling. We argue that the multi-q ground state in zero magnetic field is a prime candidate for hosting the Z2 vortex crystal proposed on the triangular Heisenberg-Kitaev model. (CD3ND3)2NaRuCl6 is the first member in an extended family of quantum triangular lattice magnets, providing a new playground to study the interplay of geometric frustration and spin-orbit effects.
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