Dong‐Yeun Koh
KAIST · Engineering
Dong-Yeun Koh 교수의 연구실은 에너지 효율적인 분리 기술과 지속 가능한 에너지 자원 개발을 핵심으로 삼고 있습니다. 특히 유기 액체 분리에 활용 가능한 탄소 분자체 여과막, 메탄 하이드레이트에서의 메탄 직접 회수 기술, 그리고 CO₂ 대체를 통한 메탄 추출 및 온실가스 감축 기술을 연구하고 있습니다. 또한 MXene 기반 웨어러블 수화젤을 활용한 고성능 생체 센서 기술 개발도 진행 중이며, 이는 산화 방지를 위한 고분자 기반 설계 전략을 포함합니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Liquid-phase separations of similarly sized organic molecules using membranes is a major challenge for energy-intensive industrial separation processes. We created free-standing carbon molecular sieve membranes that translate the advantages of reverse osmosis for aqueous separations to the separation of organic liquids. Polymer precursors were cross-linked with a one-pot technique that protected the porous morphology of the membranes from thermally induced structural rearrangement during carboni
Abstract Very recently, MXene‐based wearable hydrogels have emerged as promising candidates for epidermal sensors due to their tissue‐like softness and unique electrical and mechanical properties. However, it remains a challenge to achieve MXene‐based hydrogels with reliable sensing performance and prolonged service life, because MXene inevitably oxidizes in water‐containing system of the hydrogels. Herein, catechol‐functionalized poly(vinyl alcohol) (PVA‐CA)‐based hydrogels is proposed to inhib
The direct recovery of methane from massive methane hydrates (MHs), artificial MH-bearing clays, and natural MH-bearing sediments is demonstrated, using either CO(2) or a CO(2)/N(2) gas mixture (20 mol % of CO(2) and 80 mol % of N(2), reproducing flue gas from a power plant) for methane replacement in complex marine systems. Natural gas hydrates (NGHs) can be converted into CO(2) hydrate by a swapping mechanism. The overall process serves a dual purpose: it is a means of sustainable energy-sourc
CO2 absorption is a key to alleviating the environmental consequences of fossil fuel combustion, which is a major source of global CO2 emission. Membrane contactors have showcased several competitive advantages in CO2 absorption over conventional gas–liquid contactors (e.g., packed towers), such as a large mass-transfer area and a safe operation owing to the membranes that physically separate the gas and liquid phases. This Review discusses the state-of-the-art studies related to CO2 absorption
The direct recovery of methane from gas hydrate‐bearing sediments is demonstrated, where a gaseous mixture of CO 2 + N 2 is used to trigger a replacement reaction in complex phase surroundings. A one‐dimensional high‐pressure reactor (8 m) was designed to test the actual aspects of the replacement reaction occurring in natural gas hydrate (NGH) reservoir conditions. NGH can be converted into CO 2 hydrate by a “replacement mechanism,” which serves double duty as a means of both sustainable energy
As hydrogen molecules enter the clathrate hydrate body, the ubiquitous dodecahedral cavity (512) is too small to allow anything but single occupancy thermodynamically. The possibility that H2 double occupancy can occur in the dodecahedral cavity has been suggested and is still under debate. Here we uncover the unique feature of multiple occupancy of the hydrogen molecule in a dodecahedral cavity as induced by tuning the cage dimensions. The guest promoter population in the hydrate matrix spontan
Metal-organic frameworks (MOFs) are a class of microporous materials that have been highlighted with fast and selective sorption of gas molecules; however, they are at least partially unstable in the scale-up process. Here, we report a rational shaping of MOFs in a scalable architecture of fiber sorbent. The long-standing stability challenge of MOFs was resolved by using stable metal oxide precursors that are subject to controlled surface oxide dissolution-growth chemistry during the Mg-based MO
We report a new concept of structural transformation combined with tuning phenomena which together result in a significant increase in the hydrogen storage capacity in an icy material. It is necessary to investigate the use of a fully water-soluble structure H (sH) former so as to observe how hydrogen molecules are stably loaded into hydrate cages.
While two-dimensional (2D) Ti<sub>3</sub>C<sub>2</sub>T<sub><i>x</i></sub> MXene in aqueous dispersions spontaneously oxidizes into titanium dioxide (TiO<sub>2</sub>) nanocrystals, the crystallization mechanism has not been comprehensively understood and the resultant crystal structures are not controlled among three representative polymorphs: anatase, rutile, and brookite. In this study, such control on the lattice structures and domain sizes of the MXene-derived TiO<sub>2</sub> crystallites is
Membranes could reform the field of molecular separations by enabling new low energy manufacturing technologies. This review article discusses the current state of the art and the potential in the 2D-enabled membrane separation processes by highlighting emerging and existing areas in which robust 2D materials significantly impact the energy-efficient separation process. Analysis of 2D-enabled membrane classes and prospective materials for 2D-enabled membranes are also discussed with emphasis on
Atomic hydrogen has received recent attention because of its potential role in energy devices, silicon devices, artificial photosynthesis, hydrogen storage, and so forth. Here, we propose a highly efficient route for producing atomic hydrogen using semi-clathrate hydrates. Two major hydrogen radical sources, derived from guest/host materials, are closely examined.
Most pharmaceuticals are stereoisomers that each enantiomer shows dramatically different biological activity. Therefore, the production of optically pure chemicals through sustainable and energy-efficient technology is one of the main objectives in the pharmaceutical industry. Membrane-based separation is a continuous process performed on a large scale that uses far less energy than the conventional thermal separation process. Enantioselective polymer membranes have been developed for chiral res