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Elsa Lhotel

Publications and source records attributed to Elsa Lhotel.

At least 19 recordsLinked to original sources

Ultralow-Field Triplon Condensation in a Spin-Ladder Magnet

We realise the first ultralow-field Bose-Einstein condensation of triplons in a spin-ladder magnet, uncovering a quantum critical point at only $\mu_0 H_{c1}=0.17$ T in Henmilite ($\mathrm{Ca_2Cu(OH)_4[B(OH)_4]_2}$). Unlike dimer magnets, a ladder retains extended one-dimensional correlations in its gapped parent state, making this limit strongly fluctuation dominated. Thermodynamic, magnetoelastic, $\mu$SR, and neutron-diffraction measurements overturn the previous assignment of zero-field antiferromagnetic order, establishing a quantum-disordered coupled-ladder parent state with persistent low-energy dynamics. The weak low-temperature anomaly instead marks a gap-controlled crossover from the correlated ladder regime into the activated quantum-disordered state. These measurements further reveal an exceptionally asymmetric ordered dome extending to $\mu_0 H_{c2}\simeq 8.2$ T. Quantum Monte Carlo simulations for the relevant spin Hamiltonian place Henmilite just on the gapped side of the zero-field ladder-ordering instability, naturally accounting for the strong separation between the exchange and residual-gap scales and the tiny critical field. Our findings extend ultralow-field triplon condensation beyond the dimer paradigm and establish Henmilite as a platform for controlled tuning across quantum criticality in a fluctuation-dominated spin ladder.

cond-mat.str-el

Complex magnetic interactions in geometrically frustrated TbOF

We have identified TbOF as a unique frustrated and mixed-anion lattice, hosting unconventional magnetism. By means of magnetization, specific heat and neutron diffraction measurements down to 90 mK, as well as DFT calculations, we present a comprehensive study of the magnetic and structural properties of TbOF. We show that at 9.7 K, TbOF undergoes a structural phase transition accompanied by short-range magnetic correlations, in contrast to previously proposed long-range antiferromagnetic order. At lower temperatures, we observe two magnetic ordering transitions, consisting of incommensurate spin density waves and antiferromagnetic and ferromagnetic correlations. Furthermore, we observe metastable and hysteresis behavior below 2.0 K, highlighting the richness of complex magnetic interactions in TbOF. These results uniquely clarify the magnetic phase diagram of TbOF and highlight the intricate interplay between structure and magnetism in rare-earth oxyfluorides.

cond-mat.str-el

An inelastic neutron scattering study of the magnetic field dependence of the quantum dipolar garnet: Yb$_3$Ga$_5$O$_{12}$

The garnet compound Yb$_3$Ga$_5$O$_{12}$ is a fascinating material that is considered highly suitable for low-temperature refrigeration, via the magnetocaloric effect, in addition to enabling the exploration of quantum states with long-range dipolar interactions. It has previously been theorized that the magnetocaloric effect can be enhanced, in Yb$_3$Ga$_5$O$_{12}$ , via magnetic soft mode excitations which in the hyperkagome structure would be derived from an emergent magnetic structure formed from nanosized 10-spin loops. We study the magnetic field dependence of bands of magnetic soft mode excitations in the effective spin $S = 1/2$ hyperkagome compound Yb$_3$Ga$_5$O$_{12}$ using single crystal inelastic neutron scattering. We probe the magnetically short ranged ordered state, in which we determine magnetic nanoscale structures coexisting with a fluctuating state, and the magnetically saturated state. We determine that Yb$_3$Ga$_5$O$_{12}$ can be described as a quantum dipolar magnet with perturbative weak near-neighbor and inter-hyperkagome exchange interaction. The magnetic excitations, under the application of a magnetic field, reveal highly robust soft modes with distinctive signatures of the quantum nature of the Yb3+ spins. Our results enhance our understanding of soft modes in topological frustrated magnets that drive both the unusual physics of quantum dipolar systems and future refrigerant material design.

cond-mat.str-el

Thermodynamics of the dipole-octupole pyrochlore magnet Ce$_2$Hf$_2$O$_{7}$ in applied magnetic fields

The recently discovered dipole-octupole pyrochlore magnet Ce$_2$Hf$_2$O$_7$ is a promising three-dimensional quantum spin liquid candidate which shows no signs of ordering at low temperature. The low energy effective pseudospin-1/2 description in a magnetic field is characterized by the XYZ Hamiltonian and a Zeeman term where the dipolar local $z$-component of the pseudospin couples to the local $z$-component of the applied magnetic field, while the local $x$- and $y$-components of the pseudospin remain decoupled as a consequence of their octupolar character. Using effective Hamiltonian parameters determined in V. Poree et al., arXiv:2305.08261 (2023), remarkable experimental features can be reproduced, as for instance the specific heat and magnetization data as well as the continuum of states seen in neutron scattering. Here we investigate the thermodynamic response to magnetic fields applied along the global [110] direction using specific heat measurements and fits using numerical methods, and solve the corresponding magnetic structure using neutron diffraction. Specific heat data in moderate fields are reproduced well, however, at high fields the agreement is not satisfactory. We especially observe a two-step release of entropy, a finding that demands a review of both theory and experiment. We address it within the framework of three possible scenarios, including an analysis of the crystal field Hamiltonian not restricted to the two-dimensional single-ion doublet subspace. We conclusively rule out two of these scenarios and find qualitative agreement with a simple model of field misalignment with respect to the crystalline direction. We discuss the implications of our findings for [111] applied fields and for future experiments on Ce$_2$Hf$_2$O$_7$ and its sister compounds.

cond-mat.str-el

Impact of disorder in Nd-based pyrochlore magnets

We study the stability of the antiferromagnetic all-in--all-out state observed in dipolar-octupolar pyrochlores that have neodymium as the magnetic species. Different types of disorder are considered, either affecting the immediate environment of the Nd$^{3+}$ ion, or substituting it with a non-magnetic ion. Starting from the well studied Nd$_2$Zr$_2$O$_7$ compound, Ti substitution on the Zr site and dilution on the Nd magnetic site with La substitution are investigated. The recently discovered entropy stabilized compound NdMox, which exhibits a high degree of disorder on the non magnetic site is also studied. Using a range of experimental techniques, especially very low-temperature magnetization and neutron scattering, we show that the all-in--all-out state is very robust and withstands substitutional disorder up to large rates. From these measurements, we estimate the Hamiltonian parameters and discuss their evolution in the framework of the phase diagram of dipolar-octupolar pyrochlore magnets.

cond-mat.str-el

Dipolar-octupolar correlations and hierarchy of exchange interactions in Ce$_2$Hf$_2$O$_7$

High-resolution neutron spectroscopy on Ce$_2$Hf$_2$O$_7$ reveals a correlated state characterized by distinct dipolar scattering signals -- quasi-elastic and inelastic contributions consistent with `photon' and `spinon' excitations in quantum spin ice. These signals coexist with weak octupolar scattering. Fits of thermodynamic data using numerical methods indicate a dominant octupolar exchange, $J_{x}$ or $J_{y}$, with substantial dipolar $J_{z}$ and minute dipole-octupole $J_{xz}$ couplings. The $J_{xz}$ value is corroborated by an independent fit of the neutron scattering amplitude balance between dipolar and octupolar `photon' contributions, highlighting its importance to understand neutron scattering results in this family. Ce$_2$Hf$_2$O$_7$ enriches the landscape of dipole-octupole pyrochlore physics, and reveals a `quantum multipolar liquid' where hybrid correlations involve multiple terms in moment series expansion, opening questions on their intertwining and hierarchy in quantum phases.

cond-mat.str-el

Fractional matter coupled to the emergent gauge field in a quantum spin ice

Electronic spins can form long-range entangled phases of condensed matter named quantum spin liquids. Their existence is conceptualized in models of two- or three-dimensional frustrated magnets that evade symmetry-breaking order down to zero temperature. Quantum spin ice (QSI) is a theoretically well-established example described by an emergent quantum electrodynamics, with excitations behaving like photon and matter quasiparticles. The latter are fractionally charged and equivalent to the `spinons' emerging from coherent phases of singlets in one dimension, where clear experimental proofs of fractionalization exist. However, in frustrated magnets it remains difficult to establish consensual evidence for quantum spin liquid ground states and their fractional excitations. Here, we use backscattering neutron spectroscopy to achieve extremely high resolution of the time-dependent magnetic response of the candidate QSI material Ce$_2$Sn$_2$O$_7$. We find a gapped spectrum featuring a threshold and peaks that match theories for pair production and propagation of fractional matter excitations (spinons) strongly coupled to a background gauge field. The multiple peaks are a specific signature of the $\pi$-flux phase of QSI, providing spectroscopic evidence for fractionalization in a three-dimensional quantum spin liquid.

cond-mat.str-el

Geometric frustration on the trillium lattice in a magnetic metal-organic framework

In the dense metal-organic framework Na[Mn(HCOO)$_3$], Mn$^{2+}$ ions ($S=\frac{5}{2}$) occupy the nodes of a `trillium' hyperkagome net. We show that this material exhibits a variety of behaviour characteristic of geometric frustration: the Néel transition is suppressed well below the characteristic magnetic interaction strength; short-range magnetic order persists far above the Néel temperature; and the magnetic susceptibility exhibits a pseudo-plateau at $\frac{1}{3}$-saturation magnetisation. We demonstrate that a simple nearest-neighbour Heisenberg antiferromagnet model accounts quantitatively for each observation, and hence Na[Mn(HCOO)$_3$] is the first experimental realisation of this model on the trillium net. We develop a mapping between this trillium model and that on the two-dimensional Shastry-Sutherland lattice, and demonstrate how both link geometric frustration within the classical spin liquid regime to a strong magnetocaloric response at low fields.

cond-mat.str-el

Vibronic collapse of ordered quadrupolar ice in the pyrochore magnet Tb$_{2+x}$Ti$_{2-x}$O$_{7+y}$

While the spin liquid state in the frustrated pyrochlore Tb$_{2+x}$Ti$_{2-x}$O$_{7+y}$ has been studied both experimentally and theoretically for more than two decades, no definite description of this unconventional state has been achieved. Using synchrotron based THz spectroscopy in combination with quantum numerical simulations, we highlight a significant link between two previously unrelated features: the existence of a quadrupolar order following an ice rule and the presence of strong magneto-elastic coupling in the form of hybridized Tb$^{3+}$ crystal-field and phonon modes. The magnitude of this so-called vibronic process, which involves quadrupolar degrees of freedom, is significantly dependent on small off-stoichiometry $x$ and favors all-in all-out like correlations between quadrupoles. This mechanism competes with the long range ordered quadrupolar ice, and for slightly different stoichiometry, is able to destabilize it.

cond-mat.str-el

Crystal-field states and defect levels in candidate quantum spin ice Ce$_{2}$Hf$_{2}$O$_{7}$

We report the synthesis of powder and single-crystal samples of the cerium pyrohafnate and their characterization using neutron diffraction, thermogravimetry and X-ray absorption spectroscopy. We evaluate the amount of non-magnetic Ce$^{4+}$ defects and use this result to interpret the spectrum of crystal-electric field transitions observed using inelastic neutron scattering. The analysis of these single-ion transitions indicates the dipole-octupole nature of the ground state doublet and a significant degree of spin-lattice coupling. The single-ion properties calculated from the crystal-electric field parameters obtained spectroscopically are in good agreement with bulk magnetic susceptibility data down to about 1 K. Below this temperature, the behavior of the magnetic susceptibility indicates a correlated regime without showing any sign of magnetic long-range order or freezing down to 0.08 K. We conclude that Ce$_2$Hf$_2$O$_{7}$ is another candidate to investigate exotic correlated states of quantum matter such as the octupolar quantum spin ice recently argued to exist in the isostructural compounds Ce$_2$Sn$_2$O$_7$ and Ce$_2$Zr$_2$O$_7$.

cond-mat.str-el

Spin dynamics of the director state in frustrated hyperkagome systems

We present an experimental study of the magnetic structure and dynamics of two frustrated hyperkagome compounds, Gd3Ga5O12 and Gd3Al5O12. It has previously been shown that Gd3Ga5O12 exhibits long-range correlations of multipolar directors, that are formed from antiferromagnetic spins on loops of ten ions. Using neutron diffraction and Reverse Monte Carlo simulations we prove the existence of similar magnetic correlations in Gd3Al5O12, showing the ubiquity of these complex structures in frustrated hyperkagome materials. Using inelastic neutron scattering we shed further light on the director state and the associated low lying magnetic excitations. In addition we have measured quasielastic dynamics that show evidence of spin diffusion. Finally, we present AC susceptibility measurements on both Gd3Ga5O12 and Gd3Al5O12, revealing a large difference in the low frequency dynamics between the two otherwise similar compounds.

cond-mat.str-el

Neutron scattering by magnetic octupoles of a quantum liquid

Neutron scattering is a powerful tool to study magnetic structures and dynamics, benefiting from a precisely established theoretical framework. The neutron dipole moment interacts with electrons in materials via their magnetic field, which can have spin and orbital origins. Yet in most experimentally studied cases the individual degrees of freedom are well described within the dipole approximation, sometimes accompanied by further terms of a multipolar expansion that usually act as minor corrections to the dipole form factor. Here we report a unique example of neutrons diffracted mainly by magnetic octupoles. This unusual situation arises in a quantum spin ice where the electronic wavefunction becomes essentially octupolar under the effect of correlations. The discovery of such a new type of quantum spin liquid that comes with a specific experimental signature in neutron scattering is remarkable, because these topical states of matter are notoriously difficult to detect.

cond-mat.str-el

Strong quantum fluctuations due to competition between magnetic phases in a pyrochlore iridate

We report neutron diffraction measurements of the magnetic structures in two pyrochlore iridates, Yb2Ir2O7 and Lu2Ir2O7. Both samples exhibit the all-in-all-out magnetic structure on the Ir4+ sites below TN~ 150,K, with a low temperature moment of around 0.45 muB/Ir. Below 2\,K, the Yb moments in Yb2Ir2O7 begin to order ferromagnetically. However, even at 40 mK the ordered moment is only 0.57(3)muB/Yb, well below the saturated moment of the ground state doublet of Yb3+ (1.9 muB/Yb), deduced from magnetization measurements and from a refined model of the crystal field environment, and also significantly smaller than the ordered moment of Yb in Yb2Ti2O7 (0.9 muB/Yb). A mean-field analysis shows that the reduced moment on Yb is a consequence of enhanced phase competition caused by coupling to the all-in-all-out magnetic order on the Ir sublattice.

cond-mat.str-el

A quantum liquid of magnetic octupoles on the pyrochlore lattice

Spin liquids are highly correlated yet disordered states formed by the entanglement of magnetic dipoles$^1$. Theories typically define such states using gauge fields and deconfined quasiparticle excitations that emerge from a simple rule governing the local ground state of a frustrated magnet. For example, the '2-in-2-out' ice rule for dipole moments on a tetrahedron can lead to a quantum spin ice in rare-earth pyrochlores - a state described by a lattice gauge theory of quantum electrodynamics$^{2-4}$. However, f-electron ions often carry multipole degrees of freedom of higher rank than dipoles, leading to intriguing behaviours and 'hidden' orders$^{5-6}$. Here we show that the correlated ground state of a Ce$^{3+}$-based pyrochlore, Ce$_2$Sn$_2$O$_7$, is a quantum liquid of magnetic octupoles. Our neutron scattering results are consistent with the formation of a fluid-like state of matter, but the intensity distribution is weighted to larger scattering vectors, which indicates that the correlated degrees of freedom have a more complex magnetization density than that typical of magnetic dipoles in a spin liquid. The temperature evolution of the bulk properties in the correlated regime below 1 Kelvin is well reproduced using a model of dipole-octupole doublets on a pyrochlore lattice$^{7-8}$. The nature and strength of the octupole-octupole couplings, together with the existence of a continuum of excitations attributed to spinons, provides further evidence for a quantum ice of octupoles governed by a '2-plus-2-minus' rule. Our work identifies Ce$_2$Sn$_2$O$_7$ as a unique example of a material where frustrated multipoles form a 'hidden' topological order, thus generalizing observations on quantum spin liquids to multipolar phases that can support novel types of emergent fields and excitations.

cond-mat.str-el

Coulomb spin liquid in anion-disordered pyrochlore Tb$_2$Hf$_2$O$_7$

The charge ordered structure of ions and vacancies characterizing rare-earth pyrochlore oxides serves as a model for the study of geometrically frustrated magnetism. The organization of magnetic ions into networks of corner-sharing tetrahedra gives rise to highly correlated magnetic phases with strong fluctuations, including spin liquids and spin ices. It is an open question how these ground states governed by local rules are affected by disorder. In the pyrochlore Tb$_2$Hf$_2$O$_7$, we demonstrate that the vicinity of the disordering transition towards a defective fluorite structure translates into a tunable density of anion Frenkel disorder while cations remain ordered. Quenched random crystal fields and disordered exchange interactions can therefore be introduced into otherwise perfect pyrochlore lattices of magnetic ions. We show that disorder can play a crucial role in preventing long-range magnetic order at low temperatures, and instead induces a strongly-fluctuating Coulomb spin liquid with defect-induced frozen magnetic degrees of freedom.

cond-mat.str-el

Candidate quantum spin ice in the pyrochlore Pr$_2$Hf$_2$O$_7$

We report the low temperature magnetic properties of the pyrochlore Pr$_2$Hf$_2$O$_7$. Polycrystalline and single-crystal samples are investigated using time-of-flight neutron spectroscopy and macroscopic measurements, respectively. The crystal-field splitting produces a non-Kramers doublet ground state for Pr$^{3+}$, with Ising-like anisotropy. Below 0.5 K ferromagnetic correlations develop, which suggests that the system enters a spin ice-like state associated with the metamagnetic behavior observed at $μ_0H_c\sim2.4$~T. In this regime, the development of a discrete inelastic excitation in the neutron spectra indicates the appearance of spin dynamics which are likely related to cooperative quantum fluctuations.

cond-mat.str-el

Candidate Quantum Spin Liquid in the Ce\textsuperscript{3+} Pyrochlore Stannate Ce$_2$Sn$_2$O$_7$

We report the low temperature magnetic properties of Ce$_2$Sn$_2$O$_7$, a rare-earth pyrochlore. Our susceptibility and magnetization measurements show that due to the thermal isolation of a Kramers doublet ground state, Ce$_2$Sn$_2$O$_7$ has Ising-like magnetic moments of $\sim1.18$ $μ_\mathrm{B}$. The magnetic moments are confined to the local trigonal axes, as in a spin ice, but the exchange interactions are antiferromagnetic. Below 1 K the system enters a regime with antiferromagnetic correlations. In contrast to predictions for classical $\langle 111 \rangle$-Ising spins on the pyrochlore lattice, there is no sign of long-range ordering down to 0.02 K. Our results suggest that Ce$_2$Sn$_2$O$_7$ features an antiferromagnetic liquid ground state with strong quantum fluctuations.

cond-mat.str-el

Magnetic structure and dynamics of a strongly one-dimensional cobalt$^{II}$ metal-organic framework

We investigate the magnetism of the Co$^{II}_4$(OH)$_2$(C$_1$$_0$H$_1$$_6$O$_4$)$_3$ metal-organic framework which displays complex inorganic chains separated from each other by distances of 1 to 2 nm, and which orders at ~5.4 K. The zero-field magnetic structure is determined using neutron powder diffraction: it is mainly antiferromagnetic but posseses a ferromagnetic component along the $\textbf{c}$-axis. This magnetic structure persists in presence of a magnetic field. Ac susceptibility measurements confirm the existence of a single thermally activated regime over 7 decades in frequency ($E/k_B\approx64 K$) whereas time-dependent relaxation of the magnetization after saturation in an external field leads to a two times smaller energy barrier. These experiments probe the slow dynamics of domain walls within the chains: we propose that the ac measurements are sensitive to the motion of existing domain walls within the chains, while the magnetization measurements are governed by the creation of domain walls.

cond-mat.mtrl-sci