arXiv subjects

I. da Silva

Publications and source records attributed to I. da Silva.

3 recordsLinked to original sources

arXiv2025

Coexistence of static and dynamic local magnetic fields in an S = 3/2 honeycomb lattice antiferromagnet Co2Te3O8

Two-dimensional honeycomb lattices, characterized by their low coordination numbers, provide a fertile platform for exploring various quantum phenomena due to the intricate interplay between competing magnetic interactions, spin-orbit coupling, and crystal electric fields. Beyond the widely studied Jeff= 1/2 honeycomb systems, S = 3/2 honeycomb lattices present a promising alternative route to realizing the classical spin liquid-like state within the spin-S Kitaev models. Herein, we present crystal structure, thermodynamic, neutron diffraction and muon spin relaxation (muSR) measurements, complemented by density functional theory (DFT) calculations on an unexplored 3d transition metal based compound Co2Te3O8, where Co2+ (S = 3/2) ions form a distorted honeycomb lattice in the crystallographic bc-plane without any anti-side disorder between constituent atoms. A clear lambda type anomaly around 55 K in both magnetic susceptibility and specific heat data indicates the onset of a long-range ordered state below TN= 55 K. The dominant antiferromagnetic interaction between S = 3/2 moments is evidenced by a relatively large negative Curie-Weiss temperature of -103 K derived from magnetic susceptibility data and supported by DFT calculations. The signature of long-range antiferomagnetic order state in the thermodynamic data is corroborated by neutron diffraction and muSR results. Furthermore, muSR experiments reveal the coexistence of static and dynamic local magnetic fields below TN, along with a complex magnetic structure that can be associated with XY-like antiferromagnet, as confirmed by neutron diffraction experiments.

cond-mat.str-el↗

arXiv2018

Nuclear and Magnetic Structures of the Frustrated Quantum Antiferromagnet Barlowite, Cu$_{4}$(OH)$_{6}$FBr

Barlowite, Cu$_{4}$(OH)$_{6}$FBr, has attracted much attention as the parent compound of a new series of quantum spin liquid candidates, Zn$_{x}$Cu$_{4-x}$(OH)$_{6}$FBr. While it is known to undergo a magnetic phase transition to a long-range ordered state at $T_{N} = 15$ K, there is still no consensus over either its nuclear or magnetic structures. Here, we use comprehensive powder neutron diffraction studies on deuterated samples of barlowite to demonstrate that the only space group consistent with the observed nuclear and magnetic diffraction at low-temperatures is the orthorhombic $Pnma$ space group. We furthermore conclude that the magnetic intensity at $T < T_{N}$ is correctly described by the $Pn^\prime m^\prime a$ magnetic space group, which crucially allows the ferromagnetic component observed in previous single-crystal and powder magnetisation measurements. As such, the magnetic structure of barlowite resembles that of the related material clinoatacamite, Cu$_{4}$(OH)$_{6}$Cl$_{2}$, the parent compound of the well-known quantum spin liquid candidate hebertsmithite, ZnCu$_{3}$(OH)$_{6}$Cl$_{2}$.

cond-mat.str-el↗

arXiv2018

Evidence for $J_{\rm eff} = 0$ ground state and defect-induced spin glass behaviour in the pyrochlore osmate Y$_{2}$Os$_{2}$O$_{7}$

We present AC and DC magnetometry, heat capacity, muon spin relaxation ($μ$SR) and resonant inelastic X-ray scattering (RIXS) studies of the pyrochlore osmate Y$_2$Os$_2$O$_7$. We observe a non-zero effective moment governed by $\sqrt{f}μ_{\rm{eff}} = 0.417(1)\,μ_{\rm{B}}$ where $f$ is the fraction of Os sites which exhibit a spin, and spin freezing at temperature $T_{\rm f} \simeq 5\,$K, consistent with previous results. The field dependence of magnetisation data shows that the paramagnetic moment is most likely due to large moments $μ_{\rm eff} \simeq 3\,μ_{\rm B}$ on only a small fraction $f \simeq 0.02$ of Os sites. Comparison of single-ion energy level calculations with the RIXS data yields a non-magnetic $J_{\rm eff} = 0$ ground state on the Os$^{4+}$ sites. The spin-orbit interaction, Hund's coupling and trigonal distortion of OsO$_{6}$ octahedra are all important in modelling the experimentally observed spectra. We are able to rule out impurity effects, leaving disorder-related effects such as oxygen non-stoichiometry or site interchange between Os and Y ions as the most plausible explanation for the magnetic response in this material.

cond-mat.str-el↗