Search arXiv⌕ Search

arXiv · 2509.13542

Tuning Coupled Toroidic and Polar Orders in a Bilayer Antiferromagnet

Abstract

Magnetic toroidal order features a loop-like arrangement of magnetic dipole moments, thus breaking both spatial inversion (P) and time-reversal (T) symmetries while preserving their combined PT sym-metry. This PT symmetry enables a linear magnetoelectric effect, allowing the coupling between magnetic toroidicity and electric polarity. However, the detection and control of two-dimensional (2D) magnetic toroidal order and the investigation of its linear magnetoelectric response remain largely unexplored. Here, using bilayer CrSBr as a platform, which hosts an in-plane layer-antiferromagnetic (AFM) order and simultaneously exhibits a magnetic toroidal order, we show compelling evidence for tuning this 2D magnetic toroidicity and its induced electric polarity through magnetic-field-depend-ent second harmonic generation (SHG). Under an out-of-plane magnetic field, we decompose the SHG signal into a time-reversal-odd component that scales with the magnetic toroidal moment and a time-reversal-even component that is proportional to the electric polarization. When sweeping the magnetic field from positive to negative values, we observe that the magnetic toroidicity retains its sign but diminishes in magnitude at higher fields while the electric polarity flips its sign and increases in strength at increasing fields below a critical threshold. When applying an in-plane electric field along the Néel vector direction, together with an out-of-plane field, we find that the magnetic toroidal and electric polar domains are moved in a locked fashion. These findings underscore the promise of 2D magnetic toroidal order in realizing giant linear magnetoelectric effects, opening exciting possi-bilities for next-generation electronic, magnetic, optical, and photonic devices enabled by 2D mag-netoelectrics.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Chuangtang Wang, Xiaoyu Guo, Zixin Zhai, Meixin Cheng, Sang-Wook Cheong, Adam W. Tsen, Bing Lv, Liuyan Zhao. 2025-09-16. Tuning Coupled Toroidic and Polar Orders in a Bilayer Antiferromagnet. https://arxiv.org/abs/2509.13542

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Symmetry-induced magnetic fullerene

Defect-free, charge-neutral, pure-carbon materials are generally viewed as intrinsically non-magnetic. Here we challenge this view by establishing a fundamental principle of symmetry-induced magnetism in pure-carbon fullerene systems through molecular orbital theory. We show that high-order symmetry of fullerene molecules or their crystalline lattices induces degenerate energy levels and hence, quantised magnetic moments at half filling. This mechanism holds for all high-order symmetries. It suggests a plausible intrinsic origin for the previously debated magnetic fullerene. Additionally, recent experimental advances in the synthesis of monolayer fullerene networks provide a feasible platform to implement our prediction on the deep link between symmetry and magnetism in these systems. Our results create new, broad frontiers of quantum magnetism by introducing molecular or crystalline symmetries in any lattice.

cond-mat.mtrl-sci↗

Tritium for Nanoscale Hydrogen Analysis by Atom Probe Tomography

Accurate nanoscale detection of hydrogen is essential for understanding hydrogen-related phenomena in materials, yet conventional tracing with deuterium is often complicated by residual background hydrogen. This study evaluates tritium as a highly resolvable isotopic marker for nanoscale hydrogen analysis in metals using atom probe tomography. Titanium was selected for its ability to incorporate hydrogen isotopes, providing a suitable platform for tritium detection. Time of flight secondary ion mass spectrometry and electron backscatter diffraction were performed prior to tritium charging to characterize the initial composition and microstructure. Atom probe tomography in laser mode before and after tritium charging, at three post-charging time intervals, enables tracking of tritium incorporation over time. Thermal desorption analysis confirmed the presence of tritium and complemented the secondary ion mass spectrometry measurements, highlighting the role of the surface oxide layer in modulating tritium release. While tritium, deuterium, and protium differ in their diffusion and trapping behavior, the distinct mass signal associated with tritium provides a practical advantage for resolving hydrogen at very low concentrations. This work serves as a fundamental benchmarking study for leveraging tritium and atom probe tomography as a combined tool for understanding hydrogen in materials, relevant for interpreting local processes such as hydrogen embrittlement.

cond-mat.mtrl-sci↗

Interfacial melting as a thermodynamic indicator of solid-state synthesizability

Computational materials discovery commonly ranks candidate materials by their thermodynamic stability on the formation energy convex hull, yet many predicted-stable phases resist synthesis. We propose that solid-state synthesizability through interfacial-melt-mediated routes requires an additional thermodynamic condition: the interfacial melt at the target composition must itself remain locally stable against spinodal decomposition. We examine this in the classical Fe--B system, where thermodynamically stable FeB$_4$ has been reported under high-pressure synthesis but not in low-pressure synthesis attempts. Using melt--quench molecular dynamics driven by a fine-tuned machine-learning interatomic potential, we find that, at ambient pressure, the B-rich interfacial melt near the FeB$_4$ composition develops a concave free-energy landscape, signaling a demixing instability that is corroborated by the concentration--concentration structure factor and correlated with low-energy icosahedral and pentagonal-pyramidal boron motifs. In contrast to FeB$_4$, metastable Fe$_3$B and Fe$_{23}$B$_6$ remain synthesizable because their corresponding melts are stable. Applied pressure introduces a convex $PV$ contribution that strongly suppresses this instability, reducing the curvature at the FeB$_4$ composition to within the uncertainty of our fit at 1800~K, consistent with the experimental synthesis boundary. Comparison with CrB$_4$ further shows that weaker melt instability correlates with easier experimental synthesis. Interfacial-melt stability, which atomistic simulations can assess via the low-$k$ concentration--concentration structure factor, is thus proposed as a practical thermodynamic screening descriptor of synthesizability for AI-assisted materials discovery.

cond-mat.mtrl-sci↗