조은선 교수
Eun Seon Cho
KAIST 생명화학공학과 · 재료과학
연구실 소개
조은선 교수 연구실은 고밀도·안정성 수소 저장 소재 개발을 핵심 목표로 하며, 메탈 하이드라이드와 그래핀 유도체를 나노구조적으로 통합한 신소재를 설계하고 있습니다. 특히, 나노결정을 그래핀 옥사이드로 둘러싸는 나노캡슐화 기반의 복합재료를 통해 수소의 안정적 저장과 빠른 반응 kinetic을 동시에 구현하고자 합니다. 또한, 수소 에너지 기반의 탄소중립 사회 실현을 위해 전기화학적 에너지 변환 및 저장 소재의 설계 원리를 다각도로 연구하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Interest in hydrogen fuel is growing for automotive applications; however, safe, dense, solid-state hydrogen storage remains a formidable scientific challenge. Metal hydrides offer ample storage capacity and do not require cryogens or exceedingly high pressures for operation. However, hydrides have largely been abandoned because of oxidative instability and sluggish kinetics. We report a new, environmentally stable hydrogen storage material constructed of Mg nanocrystals encapsulated by atomical
Abstract Demand for pragmatic alternatives to carbon‐intensive fossil fuels is growing more strident. Hydrogen represents an ideal zero‐carbon clean energy carrier with high energy density. For hydrogen fuel to compete with alternatives, safe and high capacity storage materials that are readily cycled are imperative. Here, development of such a material, comprised of nickel‐doped Mg nanocrystals encapsulated by molecular‐sieving reduced graphene oxide (rGO) layers, is reported. While most work o
Abstract Ordered mesoporous carbon materials offer robust network of organized pores for energy storage and catalysis applications, but suffer from time‐consuming and intricate preparations hindering their widespread use. Here we report a new and rapid synthetic route for a N‐doped ordered mesoporous carbon structure through a preferential heating of iron oxide nanoparticles by microwaves. A nanoporous covalent organic polymer is first formed in situ covering the hard templates of assembled nano
Reverse electrodialysis (RED) directly harvests renewable energy from salinity gradients, and the achievable potential power heavily relies on the ion exchange membranes. Graphene oxides (GOs) are considered a solid candidate for the RED membrane because the laminated GO nanochannels with charged functional groups provide an excellent ionic selectivity and conductivity. Yet, a high internal resistance and poor stability in aqueous solutions limit the RED performance. Here, we develop a RED membr
Nanoencapsulation using graphene derivatives enables the facile fabrication of two-dimensional (2D) nanocomposites with unique microstructures and has been generally applied to many fields of energy materials. Particularly, metal hydrides such as MgH<sub>2</sub> encapsulated by graphene derivatives have emerged as a promising hybrid material for overcoming the disadvantageous properties of Mg-based hydrogen storage. Although the behavior of the graphene-Mg nanoencapsulation interface has been st
With global efforts to relieve the formidable impact of climate change, hydrogen is considered a viable replacement for fossil fuels without intermittency concerns of other renewable sources. Hydrogen storage plays a pivotal role in the implementation of hydrogen economy, coupling hydrogen production with fuel cell technologies. Storing hydrogen in the form of solid-state hydride materials has been studied as a future hydrogen storage technology for enabling a safe, energy-efficient, and high-en
A general problem when designing functional nanomaterials for energy storage is the lack of control over the stability and reactivity of metastable phases. Using the high-capacity hydrogen storage candidate LiAlH<sub>4</sub> as an exemplar, we demonstrate an alternative approach to the thermodynamic stabilization of metastable metal hydrides by coordination to nitrogen binding sites within the nanopores of N-doped CMK-3 carbon (NCMK-3). The resulting LiAlH<sub>4</sub>@NCMK-3 material releases H<
The roles of graphene oxide scaffolds in the nucleation and growth of Mg nanocrystals and the consequent hydrogen storage properties are revealed. This work lays the foundation for design guidelines towards more optimized hydrogen storage composites.
An emerging class of materials that are hybrid in nature is propelling a technological revolution in energy, touching many fundamental aspects of energy-generation, storage, and conservation. Hybrid materials combine classical inorganic and organic components to yield materials that manifest new functionalities unattainable in traditional composites or other related multicomponent materials, which have additive function only. This Research News article highlights the exciting materials design in
Hydrogen is a long-term clean energy carrier that enables completely carbon-free energy production. However, practical implementation of hydrogen fuel technologies is restricted because of lack of safe and high-performing storage materials. Here, we report Mg nanocrystals encapsulated by narrow, bottom-up synthesized graphene nanoribbons (GNRs) as environmentally stable and high-capacity hydrogen storage materials. As an encapsulation medium, GNRs offer similar functionalities as reduced graphen
Abstract A new pH sensor based on carbon nanotubes (CNTs), which consist of a fluorescent molecule and a CNT attached to each chain end of a pH sensitive polysulfonamide, respectively, is synthesized, and its pH sensitivity is examined in terms of the fluorescent quenching efficiency of the CNT. The pH sensitive polymeric linker shows an abrupt conformational change between an expanded coil structure and a collapsed globule structure, which results in the drastic on‐and‐off fluorescent quenching
Hydrogen is regarded as an attractive substitute for fossil fuel, but stable and safe storage of hydrogen remains a formidable challenge. In this work, a nanometer-thickness Mg nanosheet is synthesized in a one-pot system for the first time and it enables expedited hydrogen sorption through its large surface area and shortened transport paths. The Mg nanosheets absorb about 6 wt % hydrogen within 1 h without any catalyst. Also, it is demonstrated that upon adding one-dimensional carbon materials
Selective bond cleavage using a photoredox reaction is a powerful technique in the chemical conversion of biomass such as lignin since it enables us to produce value-added aromatic compounds by controlling the activation of certain chemical bonds. Also, a water-based environment would be preferred for the sake of an eco-friendly reaction, additionally having the advantage of utilizing water-originated species such as • OH and H 2 O 2 . However, a direct cleavage of the C–C bond is still challeng
대표 연구 분야
조은선 교수의 연구를 Nubint에서 더 깊이 살펴보세요
이 연구실의 논문을 앱에서 열어 AI와 함께 읽고, 핵심을 요약하고, 내 글에 인용하세요.