Jung‐Woo Yoo
Ulsan National Institute of Science and Technology · 材料科学
研究室紹介
Professor Jung-Woo Yoo's research lab specializes in the design, synthesis, and characterization of advanced functional materials, with a focus on organic and hybrid semiconductors, metal-organic frameworks (MOFs), and oxide heterostructures. The lab explores spintronics, including spin injection and transport in organic and 2D materials, as well as nonreciprocal charge transport and magnetoresistance effects in low-dimensional systems. A key direction involves engineering multifunctional materials that combine electrical conductivity, magnetic properties, and porous frameworks for applications in spintronics, catalysis, and dynamic nuclear polarization. The lab also investigates photoresponsive magnetic and conductive behaviors in organic semiconductors, aiming to develop stimuli-responsive materials for next-generation optoelectronic and spintronic devices.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15We report the spin injection and transport in ferromagnet/organic semiconductor/ferromagnet (FM/OSC/FM) heterojunctions using rubrene $({\text{C}}_{42}{\text{H}}_{28})$ as an organic semiconductor spacer. For completeness of our study, both tunneling magnetoresistance (TMR) and giant magnetoresistance (GMR) were studied by varying the thickness of the rubrene layer (5--30 nm). A thorough study of the device characteristics reveals spin-polarized carrier injection into and subsequent transport th
Abstract A polar conductor, where inversion symmetry is broken, may exhibit directional propagation of itinerant electrons, i.e., the rightward and leftward currents differ from each other, when time-reversal symmetry is also broken. This potential rectification effect was shown to be very weak due to the fact that the kinetic energy is much higher than the energies associated with symmetry breaking, producing weak perturbations. Here we demonstrate the appearance of giant nonreciprocal charge t
We report the synthesis and characterization of a two-dimensional (2D) MX<sub>2</sub>Y<sub>2</sub>-type (M = metal, X, Y = N, S, O, and X ≠ Y) copper 1,3,5-triamino-2,4,6-benzenetriol metal-organic framework (Cu<sub>3</sub>(TABTO)<sub>2</sub>-MOF). The role of oxygen in the synthesis of this MOF was investigated. Copper metal is formed along with the MOF when the synthesis is done in argon as suggested by XRD. When the reaction was exposed to air with vigorous stirring, copper metal was not obse
We report the synthesis and characterization of a two-dimensional (2D) conjugated Ni(II) tetraaza[14]annulene-linked metal organic framework (<b>NiTAA-MOF</b>) where <b>NiTAA</b> is a macrocyclic MN<sub>4</sub> (M = metal, N = nitrogen) compound. The structure of <b>NiTAA-MOF</b> was elucidated by Fourier-transform infrared, X-ray photoemission, and X-ray diffraction spectroscopies, in combination with density functional theory (DFT) calculations. When chemically oxidized by iodine, the insulati
The production of multifunctional pure organic materials that combine different sizes of pores and a large number of electron spins is highly desirable due to their potential applications as polarizers for dynamic nuclear polarization-nuclear magnetic resonance and as catalysts and magnetic separation media. Here, we report a polychlorotriphenylmethyl radical-linked covalent triazine framework (PTMR-CTF). Two different sizes of micropores were established by N<sub>2</sub> sorption and the presen
Concomitant photoinduced magnetic and electrical phenomena are reported for the organic-based magnetic semiconductor V(TCNE)x (x approximately 2; TCNE=tetracyanoethylene; magnetic ordering temperature Tc approximately 400 K). Upon optical excitation (457.9 nm), the system can be trapped in a thermally reversible photoexcited state, which exhibits reduced magnetic susceptibility and increased conductivity with a simultaneous change in IR absorption spectrum. The multiple photonic effects in V(TCN
Abstract The development of covalent organic frameworks (COFs) with efficient charge transport is of immense interest for applications in optoelectronic devices. To enhance COF charge transport properties, electroactive building blocks and dopants can be used to induce extended conduction channels. However, understanding their intricate interplay remains challenging. We designed and synthesized a tailor‐made COF structure with electroactive hexaazatriphenylene (HAT) core units and planar dioxin
Developing new linkage-based covalent organic frameworks (COFs) is one of the major topics in reticular chemistry. Electrically conductive COFs have enabled applications in energy storage and electrochemical catalysis, which are not feasible using insulating COFs. Despite significant advances, the construction of chemically stable conductive COFs by the formation of new linkages remains relatively unexplored and challenging. Here we report the solvent- and catalyst-free synthesis of a two-dimens
Although complex metal oxides with tailored compositions are increasingly in demand for applications in advanced technologies, their preparation by solution-based routes, which are typically low cost and easy to scale up, is challenging. Here, we report high-entropy layered double hydroxides (HE-LDHs) having complex compositions as precursors for complex metal oxides. Furthermore, we reveal that the ionic radii are the key factors determining the incorporation of the metal cations into the hydro
The V(TCNE){x}, x approximately 2 is an organic-based amorphous ferrimagnet, whose magnetic behavior is significantly affected in the low field regime by the random magnetic anisotropy. It was determined that this material has thermally reversible persistent change in both magnetization and conductivity driven by the optical excitation. Here, we report results of a ferrimagnetic resonance study of the photoinduced magnetism in V(TCNE){x} film. Upon optical excitation (lambda approximately 457.9
Abstract Spin thermoelectrics, an emerging thermoelectric technology, offers energy harvesting from waste heat with potential advantages of scalability and energy conversion efficiency, thanks to orthogonal paths for heat and charge flow. However, magnetic insulators previously used for spin thermoelectrics pose challenges for scale-up due to high temperature processing and difficulty in large-area deposition. Here, we introduce a molecule-based magnetic film for spin thermoelectric applications