Rare-earth tuning of magnetic entropy and interaction scales in K 3 Ln (PO 4) 2 (Ln = Yb, Gd) for adiabatic demagnetization refrigeration

arXiv:2610.28038 · cond-mat.str-el, cond-mat.mtrl-sci · Submitted 2026-10-20 · Read on arXiv

cond-mat.str-el, cond-mat.mtrl-sci

Submitted: 2026-10-20

Updated: 2026-10-20

Comments: 11 pages, 4 figures

Journal ref: Physical Review B 114, 214419 (2026)

DOI: 10.1103/gnh9-srtk

License: http://creativecommons.org/licenses/by/4.0/

The gist: Adiabatic demagnetization refrigeration (ADR) based on frustrated rare-earth magnets provides a promising route toward helium-free sub-Kelvin cooling, while balancing magnetic entropy and interaction

Abstract

Adiabatic demagnetization refrigeration (ADR) based on frustrated rare-earth magnets provides a promising route toward helium-free sub-Kelvin cooling, while balancing magnetic entropy and interaction scales is essential for optimizing the ADR functionalities. Here we investigate the low-temperature magnetic and ADR properties of the alkali rare-earth double phosphates K 3 Ln (PO 4) 2 (Ln = Yb, Gd), which crystallize in a monoclinic P2 1/m structure containing distorted isosceles triangular lattices of rare-earth ions. Magnetization and specific heat measurements confirm the absence of long-range magnetic ordering down to 0.1 K in both compounds. Direct quasi-ADR measurements demonstrate strongly contrasting refrigeration behaviors: K 3 Yb(PO 4) 2 reaches a minimum temperature of 29.8 mK from an initial state of 2 K and 6 T, whereas K 3 Gd(PO 4) 2 exhibits extended hold times below 150 mK associated with its larger magnetic entropy reservoir. Crystal-electric-field calculations confirm a J eff = 1/2 ground-state doublet in K 3 Yb(PO 4) 2, while thermodynamic analysis based on magnetic entropy and interaction scales accounts for the distinct ADR performance of the two compounds. These results identify K 3 Ln (PO 4) 2 as a chemically robust platform for rare-earth-tunable solid-state ADR.

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