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Partial up-up-down order with the continuously distributed order parameter in the triangular antiferromagnet TmMgGaO4

Published 5 Dec 2019 in cond-mat.str-el and cond-mat.mtrl-sci | (1912.02344v1)

Abstract: Frustrated quasidoublets without time-reversal symmetry can host highly unconventional magnetic structures with continuously distributed order parameters even in a single-phase crystal. Here, we report the comprehensive thermodynamic and neutron diffraction investigation on the single crystal of TmMgGaO<em>4<em>4, which entails non-Kramers Tm<sup>3+<sup>{3+} ions arranged on a geometrically perfect triangular lattice. The crystal electric field (CEF) randomness caused by the site-mixing disorder of the nonmagnetic Mg<sup>2+<sup>{2+} and Ga<sup>3+<sup>{3+} ions, merges two lowest-lying CEF singlets of Tm<sup>3+<sup>{3+} into a ground-state (GS) quasidoublet. Well below TcT_c ∼\sim 0.7 K, a small fraction of the antiferromagnetically coupled Tm<sup>3+<sup>{3+} Ising quasidoublets with small inner gaps condense into two-dimensional (2D) up-up-down magnetic structures with continuously distributed order parameters, and give rise to the \emph{columnar} magnetic neutron reflections below μ0Hc\mu_0H_c ∼\sim 2.6 T, with highly anisotropic correlation lengths, ξ</em>ab\xi</em>{ab} ≥\geq 250aa in the triangular plane and ξc\xi_c $&lt;$ cc/12 between the planes. The remaining fraction of the Tm<sup>3+<sup>{3+} ions remain nonmagnetic at 0 T and become uniformly polarized by the applied longitudinal field at low temperatures. We argue that the similar model can be generally applied to other compounds of non-Kramers rare-earth ions with correlated GS quasidoublets.

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