arXiv subjects

Margalit L. Feuer

Publications and source records attributed to Margalit L. Feuer.

3 recordsLinked to original sources

arXiv2026

Proximity-induced charge transfer, strain and magnetic exchange in graphene/CrSBr heterostructure

Stacking van der Waals materials provides a powerful route to engineer emergent electronic and magnetic behaviors through proximity-driven interactions. The graphene/CrSBr heterostructure has emerged as a compelling platform in this frontier, exhibiting exotic macroscopic responses-- including uniaxial surface-plasmon-polariton propagation and an unconventional quantum Hall effect-- indicative of strong interfacial electronic and magnetic coupling. However, a microscopic electronic landscape governing these phenomena has remained elusive. Here, we provide a comprehensive spectroscopic characterization of the graphene/CrSBr interface using a combination of angle-resolved photoemission spectroscopy (ARPES), low-energy electron microscopy (LEEM), and density functional theory. We resolve a massive redistribution of interfacial charge that concurrently hole dopes graphene and populates the quasi-one-dimensional spin-polarized conduction band of CrSBr, resulting insulator-to-metal transition in the interfacial CrSBr layer. Furthermore, electronic structure of CrSBr exhibits strong momentum-dependent renormalization distinct from conventional charge doping, and theoretical modeling supported by Raman spectroscopy points to additional interfacial compressive strain. In addition, ARPES reveals a splitting-like feature in the graphene Dirac cone consistent with spin degeneracy lifting, providing possible evidence of magnetic proximity coupling. These findings provide crucial microscopic insight into the system's optical and transport responses and establish graphene/CrSBr as a versatile platform for charge-transfer control, strain-driven band engineering, magnetic-proximity coupling, and directionally confined excitations for next-generation spintronic and nanophotonic devices.

cond-mat.str-el↗

arXiv2025

Tunable Narrowband Terahertz Radiation from van der Waals Ferroelectrics

The terahertz (THz) spectral range is central to high-speed communication, precision metrology, sensing technologies, and a range of fundamental scientific investigations. Achieving these capabilities in practical systems increasingly demands chip-scale integration of THz photonic components that are typically bulky. In this context, van der Waals (vdW) materials provide a unique platform for integrated nonlinear photonics in the visible and near-infrared regimes, and extending this framework into the THz domain would constitute a significant advance. Here, we report tunable, intense, and narrowband THz radiation from ferroelectric niobium oxyhalides. Through halogen substitution and alloying, we achieve continuous and precise control over the emission frequency from 3.1 to 5.8 THz. We show that the narrowband THz radiation is driven by phonons associated with the ferroelectric polarization. We further demonstrate dynamic and nonvolatile control of the polarity of the coherent THz wave with external electric field. This work demonstrates efficient narrowband THz emission from vdW ferroeletrics and provides microscopic insight into its origin, paving the way for on-chip THz technology for a broad range of applications.

physics.optics↗

arXiv2025

Charge Density Wave and Ferromagnetism in Intercalated CrSBr

In materials with one-dimensional electronic bands, electron-electron interactions can produce intriguing quantum phenomena, including spin-charge separation and charge density waves (CDW). Most of these systems, however, are non-magnetic, motivating a search for anisotropic materials where the coupling of charge and spin may affect emergent quantum states. Here, chemical intercalation of the van der Waals magnetic semiconductor CrSBr yields $Li_{0.17(2)} (tetrahydrofuran)_{0.26(3)} CrSBr$, which possess an electronically driven quasi-1D CDW with an onset temperature above room temperature. Concurrently, electron doping increases the magnetic ordering temperature from 132 K to 200 K and switches its interlayer magnetic coupling from antiferromagnetic to ferromagnetic. The spin-polarized nature of the anisotropic bands that give rise to this CDW enforces an intrinsic coupling of charge and spin. The coexistence and interplay of ferromagnetism and charge modulation in this exfoliatable material provides a promising platform for studying tunable quantum phenomena across a range of temperatures and thicknesses.

cond-mat.mtrl-sci↗