arXiv subjects

Sujan Shrestha

Publications and source records attributed to Sujan Shrestha.

4 recordsLinked to original sources

arXiv2026

Nanoscale Sr$_2$IrO$_4$ Freestanding Thin-Films for Flexible Electronics

We report the structural and optical properties of nanoscale Sr2IrO4 freestanding thin-films fabricated using a water-soluble Sr3Al2O6 layer. The coherent lattice structure, phonon modes, two-magnon Raman scattering, and optical absorption spectra of the Sr2IrO4 nanomembrane are analogous to those of the layered iridate epitaxial thin-films and single crystals. Remarkably, the formation of 3-unit-cell-thick SrIrO3 and interfacial composite layers alleviates antiphase boundaries at the Sr2IrO4/Sr3Al2O6 interface, resulting in structurally-robust nanomembranes. Our experimental results show that this freestanding thin-film approach of layered oxides can provide techniques for tuning or realizing unprecedented states beyond conventional thin-film methods, suggesting a pathway in achieving flexible layered-oxide electronics.

cond-mat.mtrl-sci↗

arXiv2026

Laser-Ablated Au Electrodes with Preferred Orientation and Flat Interface on Oxides

Gold (Au) thin-film electrodes deposited on oxides by pulsed laser deposition (PLD) exhibit distinctive structural properties compared with thermally evaporated Au films. While thermally evaporated Au forms polycrystalline films with randomly oriented grains, PLD-grown Au films show a strong preferred [111] orientation perpendicular to the substrate surface, likely due to the energetic nature of the laser-ablated Au plume. High-resolution transmission electron microscopy reveals atomically flat interfaces between the PLD-grown Au electrodes and epitaxial oxide thin films, separated by nanometer-scale gaps comparable to interlayer spacings in van der Waals materials. The highly ordered microstructure and flat interfacial morphology result in enhanced adhesion of the Au films to oxide surfaces. These results demonstrate that PLD can produce both high-quality Au electrodes and oxide thin films within a single deposition platform, offering improved interfacial control and potential benefits for a wide range of oxide electronic and functional devices.

cond-mat.mtrl-sci↗

arXiv2026

Gilbert Damping Parameters of Epitaxially-Stabilized Iron Gallium Thin Films from Ferromagnetic Resonance

Iron gallium (FeGa) alloys are excellent rare-earth-free magnetostrictors. Through epitaxial stabilization, the disordered A2 alloy can be extended from 19% to 30% gallium resulting in a magnetostrictive coefficient almost twice than that which is seen in rare earth magnetostrictors like SmFe2. In a composite magnetoelectric structure, this makes epitaxially-stabilized iron gallium a key material for energy-efficient beyond CMOS technologies. The energy dissipation and speed of magnetoelectric switching, however, is affected by the magnetic resonance frequency and damping. Here we report the evolution of the ferromagnetic resonance and key materials parameters (magnetic anisotropy, magnetic damping, and magnetostriction coefficient) for 70 nm thick epitaxially-stabilized single crystal A2 FeGa films beyond 19% Ga. Using flip chip ferromagnetic resonance (1-14 GHz), we find that the Gilbert damping parameter spans the range of 0.09-0.16 and decreases as the Ga concentration increases. This correlates an increasing magnetoelastic coupling with a reduction in the Gilbert damping. We find that the effective damping is a mix of contributions from the intrinsic magnon-phonon scattering and other scattering/dissipation mechanisms, with the latter being dominant especially at high Ga composition. Our results provide insight into the mechanism of magnetic relaxation in metastable high magnetostriction materials and potential switching behavior of composite magnetoelectrics.

cond-mat.mtrl-sci↗

arXiv2022

Observation of the Surface Layer of Lithium Metal using In Situ Spectroscopy

We have investigated the surface of lithium metal using x-ray photoemission spectroscopy and optical spectroscopic ellipsometry. Even if we prepare the surface of lithium metal rigorously by chemical cleaning and mechanical polishing inside a glovebox, both spectroscopic investigations show the existence of a few tens of nanometer-thick surface layers, consisting of lithium oxides and lithium carbonates. When lithium metal is exposed to room air (~50% moisture), in situ real-time monitoring of optical spectra indicates that the surface layer grows at a rate of approximately 24 nm/min, presumably driven by an interface-controlled process. Our results hint that surface-layer-free lithium metals are formidable to achieve by a simple cleaning/polishing method, suggesting that the initial interface between lithium metal electrodes and solid-state electrolytes in fabricated lithium metal batteries can differ from an ideal lithium/electrolyte contact.

cond-mat.mtrl-sci↗