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Mitchell M. Bordelon

Publications and source records attributed to Mitchell M. Bordelon.

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Directional Manipulation of a Staggered Charge Density Wave and Kondo Resonance in UTe2

UTe2 is a rare example of a correlated quantum material in which unconventional density wave orders, Kondo physics, spin-triplet pairing, and reentrant superconductivity coexist within the same electronic system. Its superconducting state develops out of a strongly correlated normal phase. The identification and control of competing or intertwined normal-state orders are thus central to elucidating the electronic landscape from which its superconductivity arises. Here, using scanning tunnelling microscopy (STM) in a vector magnetic field, we uncover a previously unreported staggered charge-density-wave (CDW) in high-quality UTe2 crystals and demonstrate its strong directional response to an external magnetic field: the staggered CDW is completely quenched by a modest 1.7 T field aligned with the quasi-one-dimensional uranium chain direction (a-axis), while remaining robust against fields along other crystallographic directions. This pronounced anisotropy is consistent with an orbital-driven mechanism that leads to a field-tuned quantum phase transition. Strikingly and counterintuitively, the same field orientation and strength concomitantly alter the hybridization gap and suppress the 5f Kondo resonance. Modelling indicates that this correlated evolution arises from a switch of the dominant hybridization channel from Te 5p- U 5f to U 6d- U 5f coupling, suggesting an intimate interplay between CDW and the Kondo effect. Our work establishes an effective tuning knob for the intertwined orders in UTe2 and provides evidence for orbital-selective Kondo hybridization, shedding light on its correlated normal state.

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Stabilization of U 5$f^2$ configuration in UTe$_2$ through U 6d dimers in the presence of Te2 chains

We investigate the topological superconductor candidate UTe$_2$ using high-resolution valence-band resonant inelastic x-ray scattering at the U $M_{4,5}$-edges. We observe atomic-like low-energy excitations that support the correlated nature of this unconventional superconductor. These excitations originate from the U $5f^2$ configuration, which is unexpected since the short Te2-Te2 distances exclude Te2 being 2-. By utilizing the photoionization cross-section dependence of the photoemission spectra in combination with band structure calculations, we infer that the stabilization of the U $5f^2$ configuration is due to the U $6d$ bonding states in the U-dimers acting as a charge reservoir. Our results emphasize that the description of the physical properties should commence with a $5f^2$ $ansatz$.

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Quantitative investigation of the short-range magnetic correlations in candidate quantum spin liquid NaYbO$_2$

We present a neutron diffraction study of NaYbO$_2$, a candidate quantum spin liquid compound hosting a geometrically frustrated triangular lattice of magnetic Yb$^{3+}$ ions. We observe diffuse magnetic scattering that persists to at least 20 K, demonstrating the presence of short-range magnetic correlations in this system up to a relatively high energy scale. Using reverse Monte Carlo and magnetic pair distribution function analysis, we confirm the predominant antiferromagnetic nature of these correlations and show that the diffuse scattering data can be well described by noninteracting layers of XY spins on the triangular lattice. We rule out Ising spins and short-range-ordered stripe or 120$^{\circ}$ phases as candidate ground states of NaYbO$_2$. These results are consistent with a possible QSL ground state in NaYbO$_2$ and showcase the benefit of combined reciprocal- and real-space analysis of materials with short-range magnetic correlations.

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Interwoven atypical quantum states in CeLiBi$_2$

We report the discovery of CeLiBi$_2$, the first example of a material in the tetragonal Ce$TX_2$ ($T$ = transition metal; $X$ = pnictogen) family wherein an alkali cation replaces the typical transition metal. Magnetic susceptibility and neutron powder diffraction measurements are consistent with a crystal-field $Γ_6$ ground state Kramers doublet that orders antiferromagnetically below $T_N = 3.4$ K with an incommensurate propagation wave vector ${\bf{k}} = (0, 0.0724(4), 0.5)$ that generates a nanometric modulation of the magnetic structure. The best model of the ordered state is an elliptical cycloid with Ce moments primarily residing in the $ab$ plane. This is highly unusual, as all other $Γ_6$ Ce$TX_2$ members order ferromagnetically. Further, we observe an atypical hard-axis metamagnetic transition at $2$ T in magnetostriction, magnetization, and resistivity measurements. CeLiBi$_2$ is a rare example of a highly conductive material with dominant skew scattering leading to a large anomalous Hall effect. Quantum oscillations with five frequencies arise in magnetostriction and magnetic susceptibility data to $T = 30$ K and $μ_0H = 55$ T, which indicate small Fermi pockets of light carriers with effective masses as low as 0.07$m_e$. Density functional theory calculations indicate that square-net Dirac-like Bi$-p$ bands are responsible for these ultralight carriers. Together, our results show that CeLiBi$_2$ enables multiple atypical magnetic and electronic properties in a single clean material.

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Novel magnetic ordering in LiYbO2 probed by muon spin relaxation

The stretched diamond lattice material LiYbO2 has recently been reported to exhibit two magnetic transitions ($T_{N1} = 1.1 K$, $T_{N2} = 0.45 K$) via specific heat, magnetization, and neutron scattering measurements [Bordelon et al., Phys. Rev. B 103, 014420 (2021)]. Here we report complementary magnetic measurements down to T = 0.28 K via the local probe technique of muon spin relaxation. While we observe a rapid increase in the zero-field muon depolarization rate at $T_{N1}$, we do not observe any spontaneous muon precession for $T < T_{N1}$, which is typically associated with long-range magnetic ordering. The depolarization rate in the ordered state shows a surprising sensitivity to magnetic fields applied along the initial spin polarization direction. Using a simple one-dimensional model, we show that these results are consistent with the unusual random-phase bipartite incommensurate magnetic structure proposed by Bordelon et al. for the intermediate temperature range $T_{N2} < T < T_{N1}$. We also find evidence for temperature-independent magnetic fluctuations persisting to our lowest temperatures, but no obvious signature of the transition or spontaneous muon precession at and below TN2, respectively. This result is suggestive of quantum dynamics within a highly degenerate ground state.

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Electronic and structural properties of RbCeX$_2$ (X$_2$: O$_2$, S$_2$, SeS, Se$_2$, TeSe, Te$_2$)

Triangular lattice delafossite compounds built from magnetic lanthanide ions are a topic of recent interest due to their frustrated magnetism and realization of quantum disordered magnetic ground states. Here we report the evolution of the structure and electronic ground states of RbCe$X_2$ compounds, built from a triangular lattice of Ce$^{3+}$ ions, upon varying their anion character ($X_2$= O$_2$, S$_2$, SeS, Se$_2$, TeSe, Te$_2$). This includes the discovery of a new member of this series, RbCeO$_2$, that potentially realizes a quantum disordered ground state analogous to NaYbO$_2$. Magnetization and susceptibility measurements reveal that all compounds manifest mean-field antiferromagnetic interactions and, with the exception of the oxide, possess signatures of magnetic correlations onset below 1 K. The crystalline electric field level scheme is explored via neutron scattering and \textit{ab initio} calculations in order to model the intramultiplet splitting of the $J=5/2$ multiplet. In addition to the two excited doublets expected within the $J=5/2$ manifold, we observe one extra, local mode present across the sample series. This added mode shifts downward in energy with increasing anion mass and decreasing crystal field strength, suggesting a long-lived anomalous mode endemic to anion motion about the Ce$^{3+}$ sites.

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Magnetic properties and signatures of moment ordering in triangular lattice antiferromagnet KCeO$_2$

The magnetic ground state and the crystalline electric field level scheme of the triangular lattice antiferromagnet KCeO$_2$ are investigated. Below $T_N =$ 300 mK, KCeO$_2$ develops signatures of magnetic order in specific heat measurements and low energy inelastic neutron scattering data. Trivalent Ce$^{3+}$ ions in the $D_{3d}$ local environment of this compound exhibit large splittings among the lowest three $4f^1$ Kramers doublets defining for the free ion the $J = 5/2$ sextet and a ground state doublet with dipole character, consistent with recent theoretical predictions in M. S. Eldeeb et al. Phys. Rev. Materials 4, 124001 (2020). An unexplained, additional local mode appears, and potential origins of this anomalous mode are discussed.

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Frustrated Heisenberg $J_1-J_2$ model within the stretched diamond lattice of LiYbO2

We investigate the magnetic properties of LiYbO$_2$, containing a three-dimensionally frustrated, diamond-like lattice via neutron scattering, magnetization, and heat capacity measurements. The stretched diamond network of Yb$^{3+}$ ions in LiYbO$_2$ enters a long-range incommensurate, helical state with an ordering wave vector ${\bf{k}} = (0.384, \pm 0.384, 0)$ that "locks-in" to a commensurate ${\bf{k}} = (1/3, \pm 1/3, 0)$ phase under the application of a magnetic field. The spiral magnetic ground state of LiYbO$_2$ can be understood in the framework of a Heisenberg $J_1-J_2$ Hamiltonian on a stretched diamond lattice, where the propagation vector of the spiral is uniquely determined by the ratio of $J_2/|J_1|$. The pure Heisenberg model, however, fails to account for the relative phasing between the Yb moments on the two sites of the bipartite lattice, and this detail as well as the presence of an intermediate, partially disordered, magnetic state below 1 K suggests interactions beyond the classical Heisenberg description of this material.

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Antiferromagnetism and crystalline-electric field excitations in tetragonal NaCeO2

We investigate the crystal structure, magnetic properties, and crystalline-electric field of tetragonal, $I4_1/amd$, NaCeO$_2$. In this compound, Ce$^{3+}$ ions form a tetragonally elongated diamond lattice coupled by antiferromagnetic interactions ($Θ_{CW} = -7.69$ K) that magnetically order below $T_N = 3.18$ K. The Ce$^{3+}$ $J = 5/2$ crystalline-electric field-split multiplet is studied via inelastic neutron scattering to parameterize a $J_{eff} = 1/2$ ground state doublet comprised of states possessing mixed $|m_z \rangle$ character. Neutron powder diffraction data reveal the onset of $A$-type antiferromagnetism with $μ=0.57(2)$ $μ_B$ moments aligned along the $c$-axis. The magnetic structure is consistent with the expectations of a frustrated Heisenberg $J_1$-$J_2$ model on the elongated diamond lattice with effective exchange values $J_1 > 4 J_2$ and $J_1 > 0$.

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High order magnon bound states in the quasi-one-dimensional antiferromagnet $α$-NaMnO$_2$

Here we report on the formation of two and three magnon bound states in the quasi-one-dimensional antiferromagnet $α$-NaMnO$_2$, where the single-ion, uniaxial anisotropy inherent to the Mn$^{3+}$ ions in this material provides a binding mechanism capable of stabilizing higher order magnon bound states. While such states have long remained elusive in studies of antiferromagnetic chains, neutron scattering data presented here demonstrate that higher order $n>2$ composite magnons exist, and, specifically, that a weak three-magnon bound state is detected below the antiferromagnetic ordering transition of NaMnO$_2$. We corroborate our findings with exact numerical simulations of a one-dimensional Heisenberg chain with easy-axis anisotropy using matrix-product state techniques, finding a good quantitative agreement with the experiment. These results establish $α$-NaMnO$_2$ as a unique platform for exploring the dynamics of composite magnon states inherent to a classical antiferromagnetic spin chain with Ising-like single ion anisotropy.

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