SearcharxivSearch

arXiv subjects

E. Pachoud

Publications and source records attributed to E. Pachoud.

12 recordsLinked to original sources

Quantum spin liquid on a 3D bipartite lattice of spin trimers stabilized by enhanced effective anisotropy

Quantum spin liquids (QSLs) represent highly entangled states of matter in which frustration-induced quantum fluctuations suppress any symmetry-breaking phase transition down to absolute zero, giving rise to fractionalized excitations and emergent gauge fields. Theoretically, bond anisotropy can stabilize QSLs even on bipartite lattices, as exemplified by the Kitaev honeycomb model; however, no material has so far been established to realize such a state as its true ground state. Here we identify the three-dimensional spin-trimer magnet KBa$_3$Ca$_4$Cu$_3$V$_7$O$_{28}$ as a promising candidate for a bipartite quantum spin liquid persisting to the lowest temperatures. Strongly coupled Cu$^{2+}$ trimers form effective pseudospin-1/2 degrees of freedom upon cooling, which in turn constitute a three-dimensional bipartite network. Bulk thermodynamic measurements, neutron scattering, $\mu$SR, and NMR detect no spin freezing or symmetry-breaking phase transition down to 20 mK, but instead reveal a gapless dynamical ground state with algebraic spin autocorrelations. Complementary Monte Carlo and exact-diagonalization calculations show that this state is stabilized by a strong enhancement of effective anisotropy: a weak microscopic Cu-Cu exchange anisotropy of approximately 15 percent is generically amplified at the trimer level, producing effective pseudospin-pseudospin interaction anisotropies of 60 to 100 percent. Our results establish trimer-based networks as a promising platform for realizing anisotropy-stabilized quantum entangled states, even in three-dimensional bipartite systems with only weak microscopic anisotropy.

cond-mat.str-el

Slow Oscillations of the Transverse Magnetoresistance in HoTe3

Slow oscillations of the magnetoresistance periodic in the inverse magnetic field with a frequency of 3.4 T have been identified in HoTe3. The temperature dependence of the oscillation amplitude is close to exponential even at low temperatures. This may be attributed to the existence of soft modes in the system and allows the estimation of the electron scattering rate on these modes. In the region of magnetic fields exceeding 1 T, the oscillations can be described as interference oscillations associated with the splitting of the band structure due to the bilayer structure of HoTe3. The obtained data have allowed us to calculate the ratio tb/tz~7.7 of the hopping integrals between layers within each bilayer (tb) and between the adjacent bilayers (tz) to estimate these integrals as tb ~ 2 meV and tz ~ 0.26 meV.

cond-mat.str-el

Ferromagnetic fragmented state in the pyrochlore Ho$_2$Ru$_2$O$_7$

The consecutive magnetic ordering of the Ho and Ru ions in the pyrochlore Ho2Ru2O7 and their interplay are investigated by neutron scattering, magnetic and specific heat measurements. The Ru moments order at 95 K into a $\Gamma_5$ easy-plane antiferromagnetic state. At 1.55 K the Ho moments order into an unusual $\Gamma_9$ ferromagnetic state with extensive ground state entropy and structured spin dynamics. It is shown how the internal fields with $\Gamma_5$ and $\Gamma_9$ geometry allow for two symmetry breaking transitions. The lower temperature ordering is driven by ruthenium mediated interactions between holmium moments as spin ice correlations develop. The unsaturated order is compatible with a fragmented ferromagnetic state equivalent to pyrochlore kagome ice.

cond-mat.str-el

Comparative study of magnetic quantum oscillations in Hall and transverse magnetoresistance

Magnetic quantum oscillations (MQO) of Hall coefficient are measured in rare-earth tritelluride TmTe$_{3}$ and shown to be much stronger and persist to higher temperature than the Shubnikov oscillations. It is general for MQO in strongly anisotropic metals, and the combined measurements of Hall and diagonal magnetoresistance provide useful informations about the electronic structure. The ratio of their MQO amplitudes depends linearly on magnetic field, and its slope gives a simple and accurate measurement tool of the electron mean free time and its temperature dependence.

cond-mat.str-el

Collective magnetic state induced by charge disorder in the non-Kramers rare-earth pyrochlore Tb$_{2}$ScNbO$_{7}$

Geometrical frustration, as in pyrochlore lattices made of corner-sharing tetrahedra, precludes the onset of conventional magnetic ordering, enabling the stabilization of fluctuating spin states at low temperature. Disorder is a subtle ingredient that can modify the nature of these exotic non-ordered phases. Here, we study the interplay between disorder and magnetic frustration in the new pyrochlore Tb$_{2}$ScNbO$_{7}$ where the non magnetic site presents a charge disorder Nb$^{5+}$/Sc$^{3+}$. Its quantification with sophisticated diffraction techniques (electrons, X-rays, neutrons) allows us to estimate the distribution of the splitting of the magnetic Tb$^{3+}$ non-Kramers ground state doublets and to compare it with excitations measured in inelastic neutron scattering. Combining macroscopic and neutron scattering measurements, we show that a clear spin glass transition at 1 K stems out while retaining strong spin liquid correlations. Our results suggest that Tb$_{2}$ScNbO$_{7}$ stabilizes one of the novel disorder induced quantum spin liquid or topological glassy phases recently proposed theoretically.

cond-mat.str-el

Two-dimensional ferromagnetic spin-orbital excitations in the honeycomb VI$_{3}$

VI$_{3}$ is a ferromagnet with planar honeycomb sheets of bonded V$^{3+}$ ions held together by van der Waals forces. We apply neutron spectroscopy to measure the two dimensional ($J/J_{c} \approx 17$) magnetic excitations in the ferromagnetic phase, finding two energetically gapped ($\Delta \approx k_{B} T_{c} \approx$ 55 K) and dispersive excitations. We apply a multi-level spin wave formalism to describe the spectra in terms of two coexisting domains hosting differing V$^{3+}$ orbital ground states built from contrasting distorted octahedral environments. This analysis fits a common nearest neighbor in-plane exchange coupling ($J$=-8.6 $\pm$ 0.3 meV) between V$^{3+}$ sites. The distorted local crystalline electric field combined with spin-orbit coupling provides the needed magnetic anisotropy for spatially long-ranged two-dimensional ferromagnetism in VI$_{3}$.

cond-mat.str-el

Kitaev interactions in the Co honeycomb antiferromagnets Na$_3$Co$_2$SbO$_6$ and Na$_2$Co$_2$TeO$_6$

Co$^{2+}$ ions in an octahedral crystal field, stabilise a j$_{eff}$ = 1/2 ground state with an orbital degree of freedom and have been recently put forward for realising Kitaev interactions, a prediction we have tested by investigating spin dynamics in two cobalt honeycomb lattice compounds, Na$_2$Co$_2$TeO$_6$ and Na$_3$Co$_2$SbO$_6$, using inelastic neutron scattering. We used linear spin wave theory to show that the magnetic spectra can be reproduced with a spin Hamiltonian including a dominant Kitaev nearest-neighbour interaction, weaker Heisenberg interactions up to the third neighbour and bond-dependent off-diagonal exchange interactions. Beyond the Kitaev interaction that alone would induce a quantum spin liquid state, the presence of these additional couplings is responsible for the zigzag-type long-range magnetic ordering observed at low temperature in both compounds. These results provide evidence for the realization of Kitaev-type coupling in cobalt-based materials, despite hosting a weaker spin-orbit coupling than their 4d and 5d counterparts.

cond-mat.str-el

Metastable and localized Ising magnetism in $α$-CoV$_{2}$O$_{6}$ magnetization plateaus

$α$-CoV$_{2}$O$_{6}$ consists of $j_{\mathrm{eff}}={1 \over 2}$ Ising spins located on an anisotropic triangular motif with magnetization plateaus in an applied field. We combine neutron diffraction with low temperature magnetization to investigate the magnetic periodicity in the vicinity of these plateaus. We find these steps to be characterized by metastable and spatially short-range ($ξ\sim$ 10 $Å$) magnetic correlations with antiphase boundaries defining a local periodicity of $\langle \hat{T}^{2} \rangle =\ \uparrow \downarrow$ to $\langle \hat{T}^{3} \rangle =\ \uparrow \uparrow \downarrow$, and $\langle \hat{T}^{4} \rangle=\ \uparrow \uparrow \downarrow \downarrow$ or $\uparrow \uparrow \uparrow \downarrow$ spin arrangements. This shows the presence of spatially short range and metastable/hysteretic, commensurate magnetism in Ising magnetization steps.

cond-mat.str-el

Charge correlation in V$_2$OPO$_4$ probed by hard x-ray photoemission spectroscopy

Electronic properties of V$_2$OPO$_4$ have been investigated by means of hard x-ray photoemission spectroscopy (HAXPES) and subsequent theoretical calculations. The V 1$s$ and 2$p$ HAXPES spectra are consistent with the charge ordering of V$^{2+}$ and V$^{3+}$. The binding energy difference between the V$^{2+}$ and V$^{3+}$ components is unexpectedly large indicating large bonding-antibonding splitting between them in the final states of core level photoemission. The V 1$s$ HAXPES spectrum exhibits a charge transfer satellite which can be analyzed by configuration interaction calculations on a V$_2$O$_9$ cluster. The V 3$d$ spectral weight near the Fermi level is assigned to the 3$d$ $t_{2g}$ orbitals of the V$^{2+}$ site. The broad V 3$d$ spectral distribution is consistent with the strong hybridization between V$^{2+}$ and V$^{3+}$ in the ground state. The core level and valence band HAXPES results indicate substantial charge transfer from the V$^{2+}$ site to the V$^{3+}$ site.7 figure

cond-mat.str-el

Spin-Orbit Excitons in CoO

CoO has an odd number of electrons in its unit cell, and therefore is expected to be metallic. Yet, CoO is strongly insulating owing to significant electronic correlations, thus classifying it as a Mott insulator. We investigate the magnetic fluctuations in CoO using neutron spectroscopy. The strong and spatially far-reaching exchange constants reported in [Sarte et al. Phys. Rev. B 98 024415 (2018)], combined with the single-ion spin-orbit coupling of similar magnitude [Cowley et al. Phys. Rev. B 88, 205117 (2013)] results in significant mixing between $j_{eff}$ spin-orbit levels in the low temperature magnetically ordered phase. The high degree of entanglement, combined with the structural domains originating from the Jahn-Teller structural distortion at $\sim$ 300 K, make the magnetic excitation spectrum highly structured in both energy and momentum. We extend previous theoretical work on PrTl$_{3}$ [Buyers et al. Phys. Rev. B 11, 266 (1975)] to construct a mean-field and multi-level spin exciton model employing the aforementioned spin exchange and spin-orbit coupling parameters for coupled Co$^{2+}$ ions on a rocksalt lattice. This parameterization, based on a tetragonally distorted type-II antiferromagnetic unit cell, captures both the sharp low energy excitations at the magnetic zone center, and the energy broadened peaks at the zone boundary. However, the model fails to describe the momentum dependence of the excitations at high energy transfers, where the neutron response decays faster with momentum than the Co$^{2+}$ form factor. We discuss such a failure in terms of a possible breakdown of localized spin-orbit excitons at high energy transfers.

cond-mat.str-el

Ordered magnetism in the intrinsically decorated $j\rm{_{eff}}$ = $\frac{1}{2}$ $α$-CoV$_{3}$O$_{8}$

The antiferromagnetic mixed valence ternary oxide $α$-CoV$_{3}$O$_{8}$ displays disorder on the Co$^{2+}$ site that is inherent to the $Ibam$ space group. The zero field structural and dynamic properties of $α$-CoV$_{3}$O$_{8}$~have been investigated using a combination of neutron and x-ray diffraction, DC susceptibility, and neutron spectroscopy. The low temperature magnetic and structural properties are consistent with a random macroscopic distribution of Co$^{2+}$ over the 16$k$ metal sites. However, by applying the sum rules of neutron scattering we observe the collective magnetic excitations are parameterized with an ordered Co$^{2+}$ arrangement and critical scattering consistent with a three dimensional Ising universality class. The low energy spectrum is well-described by Co$^{2+}$ cations coupled $via$ a three dimensional network composed of competing ferromagnetic and stronger antiferromagnetic superexchange within the $ab$ plane and along $c$, respectively. While the extrapolated Weiss temperature is near zero, the 3D dimensionality results in long range antiferromagnetic order at $T\rm{_{N}}\sim$ 19 K. A crystal field analysis finds two bands of excitations separated in energy at $\hbar ω$ $\sim$ 5 meV and 25 meV, consistent with a $j\rm{_{eff}}=\frac{1}{2}$ ground state with little mixing between spin-orbit split Kramers doublets. A comparison of our results to the random 3D Ising magnets and other compounds where spin-orbit coupling is present indicate that the presence of an orbital degree of freedom, in combination with strong crystal field effects and well-separated $j\rm{_{eff}}$ manifolds may play a key role in making the dynamics largely insensitive to disorder.

cond-mat.str-el

Disentangling orbital and spin exchange interactions for Co$^{2+}$ on a rocksalt lattice

Neutron spectroscopy was applied to study the magnetic interactions of orbitally degenerate Co$^{2+}$ on a host MgO rocksalt lattice where no long range spin or orbital order exists. The paramagnetic nature of the substituted monoxide Co$_{0.03}$Mg$_{0.97}$O allows for the disentanglement of spin-exchange and spin-orbit interactions. By considering the prevalent excitations from Co$^{2+}$ spin pairs, we extract 7 exchange constants out to the fourth coordination shell. An antiferromagnetic next nearest neighbor 180$^{\circ}$ exchange interaction is dominant, however dual ferromagnetic and antiferromagnetic interactions are observed for pairings with other pathways. These interactions can be understood in terms of a combination of orbital degeneracy in the $t_{2g}$ channel and the Goodenough-Kanamori-Anderson (GKA) rules. Our work suggests that such a hierarchy of exchange interactions exists in transition metal-based oxides with a $t_{2g}$ orbital degeneracy.

cond-mat.str-el