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arXiv · 2406.02928

Unveiling a Family of Dimerized Quantum Magnets in Ternary Metal Borides

Zhen Zhang·Andrew P. Porter·Yang Sun·Kirill D. Belashchenko·Gayatri Viswanathan·Arka Sarkar·Kirill Kovnir·Kai-Ming Ho·Vladimir Antropov
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Abstract

Dimerized quantum magnets are exotic crystalline materials where Bose-Einstein condensation of magnetic excitations can happen. However, known dimerized quantum magnets are limited to only a few oxides and halides. Here, we unveil 9 dimerized quantum magnets and 11 conventional antiferromagnets in ternary metal borides MTB$_4$ (M = Sc, Y, La, Ce, Lu, Mg, Ca, Al; T = V, Cr, Mn, Fe, Co, Ni). In this type of structure, 3d transition-metal atoms T are arranged in dimers. Quantum magnetism in these compounds is dominated by strong antiferromagnetic interactions between Cr (both Cr and Mn for M = Mg and Ca) atoms within the structural dimers, with much weaker interactions between the dimers. These systems are proposed to be close to a quantum critical point between a disordered singlet spin-dimer phase, with a spin gap, and the ordered conventional Néel antiferromagnetic phase. This new family of dimerized quantum magnets greatly enriches the materials inventory that allows investigations of the spin-gap phase. All the quantum-, conventionally-, and non-magnetic systems identified, together with experimental synthesis methods of a phase suitable for characterization, provide a platform with abundant possibilities to tune the magnetic exchange coupling by doping and study this unconventional type of quantum phase transition. This work opens up new avenues for studying the quantum magnetism of spin dimers in borides and establishes a theoretical workflow for future searches for dimerized quantum magnets in other families or types of materials.

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Zhen Zhang, Andrew P. Porter, Yang Sun, Kirill D. Belashchenko, Gayatri Viswanathan, Arka Sarkar, Kirill Kovnir, Kai-Ming Ho, Vladimir Antropov. 2024-06-05. Unveiling a Family of Dimerized Quantum Magnets in Ternary Metal Borides. https://doi.org/10.1021/jacs.4c05478

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