arXiv subjects

E. Chan

Publications and source records attributed to E. Chan.

6 recordsLinked to original sources

arXiv2026

The science of compressional heating on the LM26 magnetized target fusion experiment

The Lawson Machine 26 (LM26) at General Fusion has demonstrated compressional heating of a spherical tokamak deuterium plasma as it was compressed by an imploding solid lithium liner. Results from the first 11 compression shots on LM26 are presented, the highest-performing of which show more than a 3x increase in $T_e$, a 10x increase in $n_e$, and a 10x increase in $B_{pol}$ within the plasma driven by 3x radial compression. The experimental device and instrumentation are reviewed in detail, followed by observations about the liner trajectory and evolution of plasma properties, including increases in emission of neutrons, X-rays, and visible radiation. Observations from fast-camera images during compression provide context for interpreting the spatial structure of plasma-wall interaction. Overviews of relevant models and analysis are presented. Diagnostic data are used to reconstruct the experimental equilibrium state in computational framework as a function of time. The results build confidence in the stability and transport analyses that support the primary conclusions. Trends across the full set of 11 compression shots are presented, and detailed examinations of the high-performance shots are given individually. The central conclusions of the integrated physics model specifically indicate that compressional heating was achieved in this set of experiments, as evidenced by the balance of heating power from compression, Ohmic heating from plasma current, and losses to the boundary needed to match the experimental data. A majority of the temperature rise is attributable to compressional heating. An increase in neutron flux is also observed during compression. The results provide a basis for planned improvements to the LM26 facility that will enable the compression of magnetized plasma to increasingly higher densities and temperatures.

physics.plasm-ph↗

arXiv2026

Competing Ordering Modes in the Distorted Quantum Kagome Material Clinoatacamite Cu$_2$Cl(OH)$_3$

We have studied the magnetic properties of clinoatacamite Cu$_2$Cl(OH)$_3$, the parent compound of the quantum spin liquid candidate herbertsmithite and a longstanding puzzle among frustrated quantum magnets. As we reveal using density-functional theory, clinoatacamite belongs to the class of distorted kagome antiferromagnets with the kagome plane being embedded into a low-symmetry crystal structure. By means of thermodynamic measurements, muon spin rotation/relaxation as well as neutron diffraction on single crystals, we find in zero magnetic field complex behavior below $T_\mathrm{I}$ = 18.1 K which unfolds in three temperature regions I-III. We propose this complexity in multicritical clinoatacamite to arise from the competition of antiferromagnetic ordering modes from the underconstrained manifold of modes, which can lead to a metamagnetic texture in zero field.

cond-mat.str-el↗

arXiv2025

From hierarchical triangular spin liquid to multi-$q$ spin texture in spinel GeFe$_2$O$_4$

Combining macroscopic measurements, neutron scattering and modeling, we identify in the GeFe$_2$O$_4$ spinel a correlated paramagnetic state resulting from the predominance of third-neighbor antiferromagnetic interactions. These interactions materialize 4 isolated families of triangular planes with 120$^{\circ}$ spins emerging from the underlying pyrochlore lattice. At lower temperatures, a phase transition occurs from this hierarchical spin liquid to a non-coplanar spin texture that is characterized by 6 propagating vectors. This unusual multi-$q$ order is triggered by the presence of weaker interactions up to the sixth neighbors. The system is remarkably successful in coupling the different triangular planes while maintaining their two-dimensional 120$^{\circ}$ order. Our study highlights the hierarchy of interactions involved in GeFe$_2$O$_4$, which is singular among spinel compounds since first-neighbor interactions are only a small fraction of the dominant third neighbor ones.

cond-mat.str-el↗

arXiv2023

Acoustic lattice instabilities at the magneto-structural transition in Fe$_{1.057(7)}$Te

Fe$_{1.057(7)}$Te undergoes a first-order tetragonal to monoclinc structural transition at T$_{S} \sim 70$ K, breaking the C$_{4}$ lattice symmetry and simultaneously breaking time reversal symmetry with bicollinear magnetic order. We investigate the soft acoustic lattice dynamics near this combined magneto-structural transition. We apply spherically neutron polarimetry to study the static magnetism near this transition, characterized with x-ray powder diffraction, and find no evidence of static incommensurate magnetic correlations near the onset of monoclinic and bicollinear antiferromagnetic order. This fixes the position of our single crystal sample in the Fe$_{1+x}$Te phase diagram in the magnetic bicollinear region and illustrates that our sample statically undergoes a transition from a paramagnetic phase to a low-temperature bicollinear phase. We then apply neutron spectroscopy to study the acoustic phonons, related to elastic deformations of the lattice. We find a temperature dependent soft acoustic branch for phonons propagating along [010] and polarized along [100]. The slope of this acoustic phonon branch is sensitive to the elastic constant $C_{66}$ and the shear modulus. The temperature dependence of this branch displays a softening with a minimum near the magneto-structural transition of T$_{S}$ $\sim$ 70 K and a recovery within the magnetically ordered low temperature phase. Soft acoustic instabilities are present in the collinear phases of the chalcogenides Fe$_{1+x}$Te where nematic order found in Fe$_{1+\delta}$Se is absent. We speculate, based on localized single-ion magnetism, that the relative energy scale of magnetic spin-orbital coupling on the Fe$^{2+}$ transition metal ion is important for the presence of a nematicity in the chalcogenides.

cond-mat.str-el↗

arXiv2023

Neutron scattering sum rules, symmetric exchanges, and helicoidal magnetism in MnSb$_2$O$_6$

MnSb$_{2}$O$_{6}$ is based on the noncentrosymmetric $P321$ space group with magnetic Mn$^{2+}$ ($S={5/2}$, $L\approx 0$) spins ordering below $T_{\mathrm{N}}=12$ K in a helicoidal structure. The ground state magnetic structure, expected to be built and originate from 7 Heisenberg exchange constants, has been shown to be coupled to the underlying crystallographic chirality with polar domain switching being reported. We apply neutron spectroscopy to extract these symmetric exchange constants. Given the high complexity of the magnetic exchange network, crystallographic structure and complications fitting linear spin-wave models, we take advantage of multiplexed neutron instrumentation to use the first moment sum rule of neutron scattering to estimate the 7 exchange constants. We then use these parameters to calculate the low-energy spin-waves in the N\'eel state to reproduce the neutron response without strong antisymmetric coupling. Using Green's response functions, the stability of long-wavelength excitations in the context of proposed magnetic structures is then discussed. The results show the presence of strong exchange constants for the chiral exchange pathways and illustrate an underlying coupling between crystallographic and magnetic ``chirality" through predominantely symmetric exchange.

cond-mat.str-el↗

arXiv2022

Neutron diffraction in MnSb2O6: Magnetic and structural domains in a helicoidal polar magnet with coupled chiralities

MnSb$_{2}$O$_{6}$ is based on the structural chiral $P$321 space group #150 where the magnetic Mn$^{2+}$ moments ($S=5/2$, $L\approx 0$) order antiferromagnetically at $T_\mathrm{N}=12$ K. Unlike the related iron based langasite (Ba$_3$NbFe$_3$Si$_2$O$_{14}$) where the low temperature magnetism is based on a proper helix characterized by a time-even pseudoscalar `magnetic' chirality, the Mn$^{2+}$ ions in MnSb$_{2}$O$_{6}$ order with a cycloidal structure at low temperatures, described instead by a time-even vector `magnetic' polarity. A tilted cycloidal structure has been found [M. Kinoshita et al. Phys. Rev. Lett. 117, 047201 (2016)] to facilitate ferroelectric switching under an applied magnetic field. In this work, we apply polarized and unpolarized neutron diffraction analyzing the magnetic and nuclear structures in MnSb$_{2}$O$_{6}$ with the aim of understanding this magnetoelectric coupling. We find no evidence for a helicoidal magnetic structure with one of the spin envelope axes tilted away from the cycloidal $c$-axis. However, on application of a magnetic field $\parallel$ $\vec{c}$ the spin rotation plane can be tilted, giving rise to a cycloid-helix admixture that evolves towards a distorted helix (zero cycloidal component) for fields great than $\approx$ 2 T. We propose a mechanism for the previously reported ferroelectric switching based on coupled structural and magnetic chiralities requiring only an imbalance of structural chiral domains.

cond-mat.str-el↗