Spontaneous lattice distortion and crystal field effects in HoB4

Abstract

The tetraboride HoB4 crystallizes in a tetragonal structure (space group P4/mbm), with the Ho atoms realizing a Shastry-Sutherland lattice. It orders antiferromagnetically at TN1 = 7.1 K and undergoes further magnetic transition at TN2 = 5.7 K. The complex magnetic structures are attributed to competing order parameters of magnetic and quadrupolar origin with significant magnetoelastic coupling. Here, we investigate the response of the lattice of HoB4 across the antiferromagnetic phase transitions by using low-temperature powder x-ray diffraction and ultrasound-velocity measurements, supported by crystal electric field (CEF) calculations. Below TN2, the crystal structure of HoB4 changes to monoclinic (space group P21/b) as a macroscopic manifestation of the quadrupolar ordering. Between 300 and 3.5 K, the total distortion amplitude is 0.46~Å and the relative volume change is $3.5\times 10^{-3}$. This structural phase transition is compatible with the huge softening of the modulus $C_{44}$ observed around TN2 due to ferroquadrupolar order. A lattice instability developing immediately below TN1 is seen consistently in x-ray and ultrasound data. CEF analysis suggests a quasi-degenerated ground state for the Ho${}^{3+}$ ions in this system.

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