Superposition of ferromagnetic and antiferromagnetic spin chains in the quantum magnet BaAg2Cu[VO4]2

Abstract

Based on density functional theory band structure calculations, quantum Monte-Carlo simulations, and high-field magnetization measurements, we address the microscopic magnetic model of BaAg2Cu[VO4]2 that was recently proposed as a spin-1/2 anisotropic triangular lattice system. We show that the actual physics of this compound is determined by a peculiar superposition of ferromagnetic and antiferromagnetic uniform spin chains with nearest-neighbor exchange couplings of Ja(1) ~ -19 K and Ja(2) ~ 9.5 K, respectively. The two chains featuring different types of the magnetic exchange perfectly mimic the specific heat of a triangular spin lattice, while leaving a clear imprint on the magnetization curve that is incompatible with the triangular-lattice model. Both ferromagnetic and antiferromagnetic spin chains run along the crystallographic 'a' direction, and slightly differ in the mutual arrangement of the magnetic CuO4 plaquettes and non-magnetic VO4 tetrahedra. These subtle structural details are, therefore, crucial for the ferromagnetic or antiferromagnetic nature of the exchange couplings, and put forward the importance of comprehensive microscopic modeling for a proper understanding of quantum spin systems in transition-metal compounds.

9 pages, 9 figures, 2 tables (published version, few citations added)

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