Spin dynamics and 1/3 magnetization plateau in a coupled distorted diamond chain compound K2Cu3(MoO4)4 (2504.15216v1)

Abstract: We investigate magnetic properties of the $s$ = 1/2 compound K${2}$Cu${3}$(MoO${4}$)${4}$ by combining magnetic susceptibility, magnetization, specific heat, and electron spin resonance (ESR) with density functional calculations. Its monoclinic structure features alternating Cu$^{2+}$ ($s$ = 1/2) monomers and edge-shared dimers linked by MoO${4}$ units, forming a distorted diamond chain along the $a$-axis. Antiferromagnetic order occurs at $T{\rm N}$ = 2.3 K, as evident from a $\lambda$-type anomaly in specific heat and magnetic susceptibility derivatives. Inverse magnetic susceptibility reveals coexisting ferro- and antiferromagnetic interactions. Specific heat and ESR data show two characteristic temperatures: one at 20 K, associated with spin-singlet formation in Cu${2}$O${9}$ dimers, and another at 3.68 K, indicating short-range correlations between dimers and monomers. Magnetization measurements reveal a metamagnetic transition at 2.6 T and a critical magnetic field $\mu_{0}H_{c}$ = 3.4 T, where a 1/3 magnetization plateau emerges with saturation near 0.35 $\mu_{\rm B}$. Low-temperature specific heat and magnetization data reveal the suppression of long-range order at $\mu_{0}H_{c}$, enabling the construction of a temperature-magnetic field phase diagram showing multiple magnetic phases near the $\mu_{0}H_{c}$. Density functional theory confirms a distorted diamond chain with $J_{1}$ dimers and competing $J_2$, $J_4$, $J_3$, and $J_5$ interactions with monomer spins as an effective low-temperature spin model.