arXiv subjects

Min-Hyoung Jung

Publications and source records attributed to Min-Hyoung Jung.

5 recordsLinked to original sources

arXiv2026

Ballistic transport in nanodevices based on single-crystalline Cu thin film

In ballistic transport, the movement of charged carriers is essentially unimpeded by scattering events. In this limit, microscopic parameters such as crystal momentum, spin and quantum phases are well conserved, allowing electrons to maintain their quantum coherence over longer distances. Nanoscale materials, like carbon nanotubes, graphene, and nanowires, exhibit ballistic transport. However, their scalability in devices is significantly limited. While deposited metal films offer excellent scalability for nanodevices, achieving ballistic transport in these films poses a challenge due to their short electronic mean free path. Here, we investigated the electronic transport in cross-geometry devices fabricated with 90 nm-thick copper films without grain boundaries. We observed ballistic transport in devices with channel width smaller than 150 nm below 85 K by measuring negative bend resistance. Our findings would open the opportunity for probing intrinsic quantum properties of Cu, and for realizing scalable low-loss signal transmission and high-quality interconnects in semiconductor devices.

cond-mat.mes-hall↗

arXiv2026

Establishing Atomic Coherence in Twisted Oxide Membranes Containing Volatile Elements

Twisted oxide membranes represent a promising platform for exploring moire physics and emergent quantum phenomena. However, the presence of amorphous interfacial dead layers in conventional oxide heterostructures impedes coherent coupling and suppresses moire-induced interactions. While high-temperature thermal treatments can facilitate interfacial bonding, additional care is needed for materials containing volatile elements, where elevated temperatures may cause elemental loss. This study demonstrates the realization of atomically coherent, chemically bonded interface in twisted NaNbO3 heterostructures through controlled oxygen-annealing treatment. Atomic-resolution imaging and spectroscopy reveal ordered perovskite registry accompanied by systematic lattice contraction and modified electronic structure at the twisted interface, providing signatures of chemical reconstruction rather than physical adhesion. This reconstructed interface mediates highly asymmetric strain propagation in which the bottom membrane remains nearly relaxed while the top membrane accommodates substantial shear strain, thereby establishing a strain gradient that enables long-range electromechanical coupling throughout the twisted oxide membranes. By resolving the nature of the reconstructed interface, these findings establish a robust pathway for achieving coherent and strain-tunable oxide moire superlattices, opening pathways to engineer emergent ferroic and electronic functionalities.

cond-mat.mtrl-sci↗

arXiv2025

Universal Fabrication of Graphene/Perovskite Oxide Hybrid Heterostructures

Hybrid heterostructures composed of graphene and perovskite oxides provide a promising platform for exploiting synergetic interfacial functionalities. Conventional fabrication methods of the hybrid heterostructures rely on transferring graphene grown on metallic substrates-- a process that is time-consuming, labor-intensive, and prone to introducing numerous defects. In this study, we present a universal, catalyst-free method for the direct growth of graphene on insulating substrates by employing three different perovskite oxide substrates (SrTiO$_3$, LaAlO$_3$, and (La$_{0.18}$Sr$_{0.82}$)(Al$_{0.59}$Ta$_{0.41}$)O$_3$) using atmospheric chemical vapor deposition. Comprehensive characterization via Raman spectroscopy, X-ray spectroscopy, scanning probe microscopy, and electron microscopy confirmed the formation of a uniform, continuous monolayer graphene on all substrates. We identified that growth temperature critically governs graphene quality, as excessive active species may lead to secondary nucleation and the formation of multilayer graphene. Notably, all substrates shared the same optimal growth conditions. Low-temperature Raman spectroscopy and scanning tunneling microscopy of the graphene/SrTiO$_3$ hybrid heterostructure revealed cooperative phenomena, including substrate-induced lattice-phonon and electron-phonon coupling. Our work establishes a reproducible, transfer-free fabrication route for graphene/perovskite oxide hybrid heterostructures and provides empirical support for the universal growth of graphene on insulating substrates.

cond-mat.mtrl-sci↗

arXiv2023

Machine-learning-assisted analysis of transition metal dichalcogenide thin-film growth

In situ reflective high-energy electron diffraction (RHEED) is widely used to monitor the surface crystalline state during thin-film growth by molecular beam epitaxy (MBE) and pulsed laser deposition. With the recent development of machine learning (ML), ML-assisted analysis of RHEED videos aids in interpreting the complete RHEED data of oxide thin films. The quantitative analysis of RHEED data allows us to characterize and categorize the growth modes step by step, and extract hidden knowledge of the epitaxial film growth process. In this study, we employed the ML-assisted RHEED analysis method to investigate the growth of 2D thin films of transition metal dichalcogenides (ReSe2) on graphene substrates by MBE. Principal component analysis (PCA) and K-means clustering were used to separate statistically important patterns and visualize the trend of pattern evolution without any notable loss of information. Using the modified PCA, we could monitor the diffraction intensity of solely the ReSe2 layers by filtering out the substrate contribution. These findings demonstrate that ML analysis can be successfully employed to examine and understand the film-growth dynamics of 2D materials. Further, the ML-based method can pave the way for the development of advanced real-time monitoring and autonomous material synthesis techniques.

cond-mat.mtrl-sci↗

arXiv2022

Reversibly controlled ternary polar states and ferroelectric bias promoted by boosting square-tensile-strain

Interaction between dipoles often emerges intriguing physical phenomena, such as exchange bias in the magnetic heterostructures and magnetoelectric effect in multiferroics, which lead to advances in multifunctional heterostructures. However, the defect-dipole tends to be considered the undesired to deteriorate the electronic functionality. Here, we report deterministic switching between the ferroelectric and the pinched states by exploiting a new substrate of cubic perovskite, BaZrO$_{3}$, which boosts square-tensile-strain to BaTiO$_{3}$ and promotes four-variants in-plane spontaneous polarization with oxygen vacancy creation. First-principles calculations propose a complex of an oxygen vacancy and two Ti$^{3+}$ ions coins a charge-neutral defect-dipole. Cooperative control of the defect-dipole and the spontaneous polarization reveals ternary in-plane polar states characterized by biased/pinched hysteresis loops. Furthermore, we experimentally demonstrate that three electrically controlled polar-ordering states lead to switchable and non-volatile dielectric states for application of non-destructive electro-dielectric memory. This discovery opens a new route to develop functional materials via manipulating defect-dipoles and offers a novel platform to advance heteroepitaxy beyond the prevalent perovskite substrates.

cond-mat.mtrl-sci↗