arXiv subjects

Kaushick K. Parui

Publications and source records attributed to Kaushick K. Parui.

7 recordsLinked to original sources

arXiv2026

Disorder-driven magnetic duality in the spin-$\frac{1}{2}$ system ktenasite, Cu$_\text{2.7}$Zn$_\text{2.3}$(SO$_\text{4}$)$_\text{2}$(OH)$_\text{6}\cdot$6H$_\text{2}$O

Disorder in frustrated quantum systems can critically influence their magnetic ground states and drive exotic correlated behavior. In the $S = \frac{1}{2}$ system ktenasite, Cu$_\text{2.7}$Zn$_\text{2.3}$(SO$_\text{4}$)$_\text{2}$(OH)$_\text{6}\cdot$6H$_\text{2}$O, we show that structural disorder drives an unexpected dimensional crossover and stabilizes a rare coexistence of distinct magnetic states. Neutron diffraction reveals significant Cu/Zn mixing at the Cu2 site, which tunes the Cu$^{2+}$ sublattice from a two-dimensional scalene-distorted triangular lattice into a one-dimensional spin-chain network. Magnetic susceptibility, neutron diffraction, ac susceptibility, and specific heat measurements collectively indicate magnetic duality: a coexistence of incommensurate long-range magnetic order below $T_\text{N} = 4\,$K and a cluster spin-glass state with $T_\text{f} = 3.28\,$K at $ν= 10\,$Hz. Our findings highlight ktenasite as a rare platform where structural disorder tunes the effective dimensionality and stabilizes coexisting ordered and glassy magnetic phases, offering a unique opportunity to explore the interplay of frustration, disorder, and dimensional crossover in quantum magnets.

cond-mat.str-el↗

arXiv2026

Spin-liquid-like ground states in the double hydroxyperovskites CuSn(OD)6 and MnSn(OD)6 evidenced by μSR spectroscopy

Double hydroxide perovskites with magnetic transition-metal ions were recently identified as a unique class of materials that combine magnetic frustration with correlated proton disorder-a prerequisite for quantum-disordered fluctuating magnetic ground states resembling spin liquids. Here we present the results of muon spin relaxation (μSR) measurements carried out on fully deuterated samples of the double hydroxyperovskites CuSn(OH)6 (S = 1/2) and MnSn(OH)6 (S = 5/2) over the temperature range 0.053-50 K. The absence of any long-range magnetic order is confirmed down to 0.053 K. We observe no oscillations of the muon asymmetry down to the lowest temperature. The muon relaxation rates show a continuous increase with decreasing temperature, indicating persistent spin fluctuations in both compounds. Spin correlations are consistent with homogeneous spin dynamics. These observations reinforce the assertion that both compounds have a quantum-dynamic magnetic ground state that is consistent with a spin-liquid-like phase stabilized by proton disorder.

cond-mat.str-el↗

arXiv2025

Spin Liquid Mimicry in the Hydroxide Double Perovskite CuSn(OH)$_6$ Induced by Correlated Proton Disorder

The face-centered-cubic lattice is composed of edge-sharing tetrahedra, making it a leading candidate host for strongly frustrated magnetism, but relatively few face-centered frustrated materials have been investigated. In the hydroxide double perovskite CuSn(OH)$_6$, magnetic frustration of the Cu$^{2+}$ quantum spins is partially relieved by strong Jahn-Teller distortions. Nevertheless, the system shows no signs of long-range magnetic order down to 45 mK and instead exhibits broad thermodynamic anomalies in specific heat and magnetization, indicating short-range dynamical spin correlations-a behavior typical of quantum spin liquids. We propose that such an unusual robustness of the spin-liquid-like state is a combined effect of quantum fluctuations of the quantum spins $S=\frac{1}{2}$, residual frustration on the highly distorted face-centered Cu$^{2+}$ sublattice, and correlated proton disorder. Similar to the disorder-induced spin-liquid mimicry in YbMgGaO$_4$ and herbertsmithite, proton disorder destabilizes the long-range magnetic order by introducing randomness into the magnetic exchange interaction network. However, unlike the quenched substitutional disorder on the magnetic sublattice, which is difficult to control, proton disorder can in principle be tuned through pressure-driven proton ordering transitions. This opens up the prospect of tuning the degree of disorder in a magnetic system to better understand its influence on the magnetic ground state.

cond-mat.str-el↗

arXiv2025

Disordered ground state in the three-dimensional face-centred frustrated spin-$\frac{5}{2}$ system MnSn(OH)$_\text{6}$

Frustrated magnetism in face-centred cubic (fcc) magnetic sublattices remains underexplored but holds considerable potential for exotic magnetic behaviour. Here we report on the crystal structure, magnetic and thermodynamic properties of the $A$-site-vacant double hydroxide perovskite MnSn(OH)$_6$. Despite dominant antiferromagnetic interactions among Mn$^{2+}$ moments, evidenced by a negative Curie-Weiss temperature, the lack of a sharp thermodynamic transition down to 350$\,$mK implies the absence of long-range magnetic order. However, a broad hump in the specific heat at 1.6$\,$K suggests short-range correlations. Neutron diffraction at low temperatures confirms the presence of three-dimensional antiferromagnetic correlations, manifested as diffuse magnetic scattering with a correlation length $ξ= 24.66\,$Å and magnetic propagation vectors $\mathbf{k}=(\frac{1}{2}\,\frac{1}{2}\,\frac{1}{2})$ and $(0\,0.625\,0)$ at 20$\,$mK.

cond-mat.str-el↗

arXiv2025

Stacking disorder in novel ABAC-stacked brochantite, Cu$_4$SO$_4$(OH)$_6$

In geometrically frustrated magnetic systems, weak interactions or slight changes to the structure can tip the delicate balance of exchange interactions, sending the system into a different ground state. Brochantite, Cu$_4$SO$_4$(OH)$_6$, has a copper sublattice composed of distorted triangles, making it a likely host for frustrated magnetism, but exhibits stacking disorder. The lack of synthetic single crystals has limited research on the magnetism in brochantite to powders and natural mineral crystals. We grew crystals which we find to be a new polytype with a tendency toward ABAC stacking and some anion disorder, alongside the expected stacking disorder. Comparison to previous results on natural mineral specimens suggests that cation disorder is more deleterious to the magnetism than anion and stacking disorder. Our specific heat data suggest a double transition on cooling into the magnetically ordered state.

cond-mat.str-el↗

arXiv2025

Correlated proton disorder in the crystal structure of the double hydroxide perovskite CuSn(OH)$_6$

CuSn(OH)$_6$ is a quantum spin system from the family of magnetic double perovskite hydroxides, having a frustrated magnetic sublattice. It is also known as the natural mineral mushistonite, whose crystal structure has remained elusive for decades. Here we employ x-ray and neutron powder diffraction to solve the crystal structure of CuSn(OH)$_6$ and propose a structure model in the orthorhombic space group $Pnnn$ with correlated proton disorder. The occupation of the hydrogen sites in the structure is constrained by ``ice rules'' similar to those known for water ice. The resulting frustration of the hydrogen bonding network is likely to have a complex and interesting interplay with the strong magnetic frustration expected in the face-centred magnetic sublattice. Structural distortions, which are quite pronounced in Cu$^{2+}$ compounds due to the Jahn-Teller effect, partially alleviate both types of frustration. We also show that hydrostatic pressure tends to suppress proton disorder through a sequence of proton-ordering transitions, as some of the split hydrogen sites merge already at 1.75 GPa while others show a tendency toward possible merging at higher pressures.

cond-mat.mtrl-sci↗

arXiv2024

Magnetic Phase Diagram of Rouaite, Cu$_2$(OH)$_3$NO$_3$

Spinon-magnon mixing was recently reported in botallackite Cu$_2$(OH)$_3$Br with a uniaxially compressed triangular lattice of Cu$^{2+}$ quantum spins [Zhang et al., Phys. Rev. Lett. 125, 037204 (2020)]. Its nitrate counterpart rouaite, Cu$_2$(OH)$_3$NO$_3$, has a highly analogous structure and might be expected to exhibit similar physics. To lay a foundation for research on this material, we clarify rouaite's magnetic phase diagram and identify both low-field phases. The low-temperature magnetic state consists of alternating ferro- and antiferromagnetic chains, as in botallackite, but with additional canting, leading to net moments on all chains which rotate from one chain to another to form a 90$^\circ$ cycloidal pattern. The higher-temperature phase is a helical modulation of this order, wherein the spins rotate from one Cu plane to the next. This extends to zero temperature for fields perpendicular to the chains, leading to a set of low-temperature field-induced phase transitions. Rouaite may offer another platform for spinon-magnon mixing, while our results suggest a delicate balance of interactions and high tunability of the magnetism.

cond-mat.str-el↗