arXiv subjects

D. P. Sari

Publications and source records attributed to D. P. Sari.

5 recordsLinked to original sources

arXiv2026

Non-magnetic ground state in A$_2$WCl$_6$ (A = Cs, Rb, K): A face-centered cubic system of spin-orbit-entangled $J$ = 2 states

Heavy transition metal compounds with strong spin-orbit coupling appeared as a platform for $d$-electron multipolar physics. We report the electronic, magnetic, and structural properties of antifluorite-type tungsten chloride A$_2$WCl$_6$ (A = Cs, Rb, and K), comprising a face-centered cubic lattice of W$^{4+}$ ions. The 5$d^2$ configuration of W$^{4+}$ ions in a cubic environment yields a spin-orbit-entangled $J$ = 2 state, which has been discussed to give rise to multipolar ordering such as charge quadrupolar or magnetic octupolar ordering. We found that K$_2$WCl$_6$ undergoes a cubic-to-tetragonal structural transition which lifts the degeneracy of the $J$ = 2 state, leading to a non-magnetic singlet ground state. By contrast, Rb$_2$WCl$_6$ and Cs$_2$WCl$_6$ show no signs of phase transition and remain non-magnetic down to the lowest temperature measured. At low temperatures, signatures of weak structural anomalies were revealed, which may point to the presence of local distortions of the WCl$_6$ octahedra. We argue that the subtle structural distortion arises from the local quadrupolar component of the $J$ = 2 state but the frustrated quadrupolar interaction, together with chemical disorder, inhibits the formation of long-range quadrupolar ordering.

cond-mat.str-el↗

arXiv2024

Field-Induced Criticality in YbCu4Au

YbCu4Au is a unique material exhibiting multiple quantum fluctuations simultaneously. In this study, we investigated the field-induced criticality in YbCu4Au, based on comprehensive micro and macro measurements, including powder X-ray diffraction (XRD), neutron powder diffraction (NPD), nuclear magnetic resonance, magnetization, resistivity, specific heat, muon spin rotation relaxation (muSR), and X-ray absorption spectroscopy (XAS). Single crystals of YbCu4Au were grown, and their crystal structure was determined using XRD, and NPD measurements. Magnetic successive transitions were observed below 1 T by specific heat, resistivity, NPD, and muSR measurements. XAS measurements further indicate that the valence of Yb ions (+2.93) remained unchanged above 2 T. Moreover, the change in quadrupole frequency observed in the previous study is attributable to the electric quadrupole, as the expected value of the electric quadrupole was finite under magnetic fields [S. Wada et al., Journal of Physics: Condensed Matter, 20, 175201 (2008).]. These experimental results suggest that YbCu4Au exhibited bicritical behavior near 1 T, arising from the competition between RKKY interaction, accounting for the magnetic phases, and the Zeeman effect.

cond-mat.str-el↗

arXiv2022

Antiferromagnetic ordering of organic Mott insulator $λ$-(BEDSe-TTF)$_2$GaCl$_4$

The band structure and magnetic properties of organic charge-transfer salt $λ$-(BEDSe-TTF)$_2$GaCl$_4$ (BEDSe-TTF: bis(ethylenediseleno)tetrathiafulvalene; abbreviated as $λ$-BEDSe) are investigated. The reported crystal structure is confirmed using X-ray diffraction measurements, and the transfer integrals are calculated. The degree of electron correlation $U/W$ ($U$: on-site Coulomb repulsion, $W$: bandwidth) of $λ$-BEDSe is larger than one and comparable to that of the isostructural Mott insulator $λ$-(ET)$_2$GaCl$_4$ (ET: bis(ethylenedithio)tetrathiafulvalene, abbreviated as $λ$-ET), whereas the $U/W$ of the superconducting salt $λ$-(BETS)$_2$GaCl$_4$ (BETS: bis(ethylenedithio)tetraselenafulvalene) is smaller than one. $^{13}$C-NMR and $μ$SR measurements revealed that $λ$-BEDSe undergoes an antiferromagnetic (AF) ordering below $T_{\rm N} = 22$~K. In the AF state, discrete $^{13}$C-NMR spectra with a remaining central peak are observed, indicating the commensurate AF spin structure also observed in $λ$-ET. The similarity between the structural and magnetic properties of $λ$-BEDSe and $λ$-ET suggests that both salts are in the same electronic phase, i.e., the physical properties of $λ$-BEDSe can be understood by the universal phase diagram of bandwidth-controlled $λ$-type organic conductors obtained by donor molecule substitution.

cond-mat.str-el↗

arXiv2022

Competing spin-orbital singlet states in the 4$d^4$ honeycomb ruthenate Ag$_3$LiRu$_2$O$_6$

When spin-orbit-entangled $d$-electrons reside on a honeycomb lattice, rich quantum states are anticipated to emerge, as exemplified by the $d^5$ Kitaev materials. Distinct yet equally intriguing physics may be realized with a $d$-electron count other than $d^5$. We found that the layered ruthenate Ag$_3$LiRu$_2$O$_6$ with $d^4$ Ru$^{4+}$ ions at ambient pressure forms a honeycomb lattice of spin-orbit-entangled singlets, which is a playground for frustrated excitonic magnetism. Under pressure, the singlet state does not develop the expected excitonic magnetism but experiences two successive transitions to other nonmagnetic phases, first to an intermediate phase with moderate distortion of honeycomb lattice, and eventually to a high-pressure phase with very short Ru-Ru dimer bonds. While the strong dimerization in the high-pressure phase originates from a molecular orbital formation as in the sister compound Li$_2$RuO$_3$, the intermediate phase represents a spin-orbit-coupled $J$-dimer state which is stabilized by the admixture of upper-lying $J_{\rm eff} = 1$-derived states. We argue that the $J$-dimer state is induced by a pseudo-Jahn-Teller effect associated with the low-lying spin-orbital excited states and is unique to spin-orbit-entangled $d^4$ systems. The discovery of competing singlet phases demonstrates rich spin-orbital physics of $d^4$ honeycomb compounds and paves the way for realization of unconventional magnetism.

cond-mat.str-el↗

arXiv2021

Formation of orbital molecules on a pyrochlore lattice induced by A-O bond covalency

The pyrochlore ruthenate In$_2$Ru$_2$O$_7$ displays a subtle competition between spin-orbital entanglement and molecular orbital formation. At room temperature, a spin-orbit-entangled singlet state was identified. With decreasing temperature, In$_2$Ru$_2$O$_7$ undergoes multiple structural transitions and eventually forms a nonmagnetic ground state with semi-isolated Ru$_2$O units on the pyrochlore lattice. The dominant hopping through the Ru-O-Ru linkage leads to molecular orbital formation within the Ru$_2$O units. This molecular orbital formation is unique in that it involves the O$^{2-}$ anions, unlike the transition-metal dimers observed in systems with edge-sharing octahedra. We argue that the covalent character of In-O bonds plays a pivotal role in the structural transitions and molecular orbital formation and such bonding character of "$A$-site" ions is an important ingredient for electronic phase competition in complex transition metal oxides.

cond-mat.str-el↗