Yun Jung Lee
한양대학교 공과대학 기계공학과 · 공학
윤정리 교수의 연구실은 바이오 유기체를 활용한 나노소재 합성과 에너지 저장 장치의 혁신을 핵심으로 삼고 있습니다. 특히 유전자 조작을 통해 기능성을 부여한 바이러스를 나노구조 전극 재료의 템플릿으로 활용하여 리튬이온 배터리의 고출력 및 고용량 성능을 극대화하고 있습니다. 또한 유연한 에너지 저장 장치 개발을 위해 스마트 섬유 기반 전류수집체와 나노구조 산화물의 융합 연구도 진행 중입니다. 자연의 수분 통로인 아คว아포린을 모방한 그래핀 옥사이드 막을 통한 수질 정화 기술 개발도 함께 추진하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Development of materials that deliver more energy at high rates is important for high-power applications, including portable electronic devices and hybrid electric vehicles. For lithium-ion (Li+) batteries, reducing material dimensions can boost Li+ ion and electron transfer in nanostructured electrodes. By manipulating two genes, we equipped viruses with peptide groups having affinity for single-walled carbon nanotubes (SWNTs) on one end and peptides capable of nucleating amorphous iron phospha
We report the synthesis and electrochemical activity of gold and silver noble metals and their alloy nanowires using multiple virus clones as anode materials for lithium ion batteries. Using two clones, one for specificity (p8#9 virus) and one versatility (E4 virus), noble metal nanowires of high-aspect ratio with diameters below 50 nm were successfully synthesized with control over particle sizes, morphologies, and compositions. The biologically derived noble metal alloy nanowires showed electr
Amorphous iron phosphate nanowires with diameters of 10 to 20 nm were synthesized using genetically engineered M13 virus for lithium ion battery cathodes. Hydrolysis of Fe3+ ions has been effectively suppressed by forming conjugates with the virus and synthesizing at low temperature, 4 °C. The M13 virus biological template facilitated elaborate nanostructure design and environmentally benign, low temperature synthesis. By implementing heterostructures with silver, we demonstrated experimentally
NdBa<sub>0.75</sub>Ca<sub>0.25</sub>Co<sub>2</sub>O<sub>5+δ</sub>-based double perovskite catalysts provide new ways for significantly enhanced oxygen-related electrochemical reactions with durable characteristics in alkaline atmospheres.
Increasing demand for flexible devices in various applications, such as smart watches, healthcare, and military applications, requires the development of flexible energy-storage devices, such as lithium-ion batteries (LIBs) with high flexibility and capacity. However, it is difficult to ensure high capacity and high flexibility simultaneously through conventional electrode preparation processes. Herein, smart conductive textiles are employed as current collectors for flexible LIBs owing to their
This review covers various strategies aimed at controlling Li deposition on a heterogeneous current collector for an anodeless cell configuration in batteries with liquid and solid-state electrolytes.
Abstract Water purification by membranes is widely investigated to address concerns related to the scarcity of clean water. Achieving high flux and rejection simultaneously is a difficult challenge using such membranes because these properties are mutually exclusive in common artificial membranes. Nature has developed a method for this task involving water‐channel membrane proteins known as aquaporins. Here, the design and fabrication of graphene oxide (GO)‐based membranes with a surface‐tethere
Core-shell carbon-coated LiFePO4 nanoparticles were hybridized with reduced graphene (rGO) for high-power lithium-ion battery cathodes. Spontaneous aggregation of hydrophobic graphene in aqueous solutions during the formation of composite materials was precluded by employing hydrophilic graphene oxide (GO) as starting templates. The fabrication of true nanoscale carbon-coated LiFePO4 -rGO (LFP/C-rGO) hybrids were ascribed to three factors: 1) In-situ polymerization of polypyrrole for constrained
We report a facile and template-free soft chemical approach that employs a low-temperature calcination treatment to synthesize a new class of materials comprising self-arranged hollow mesoporous Co3O4 and Co3O4–carbon nanotube composites. Each hollow particle is formed by a double-layered nanowall with a thickness of around 50–100 nm. The inner wall consists of a uniform amorphous layer, while the outer layer consists of self-assembled aggregates of ultrafine nanoflakes and particles. Our synthe
Li-free all-solid-state batteries can achieve high energy density and safety. However, separation of the current collector/solid electrolyte interface during Li deposition increases interfacial resistance, which deteriorates safety and reversibility. In this study, a reversible 3D porous anode is designed based on Li deposition behavior that depends on the pore size of the anode. More Li deposits are accommodated within the smaller pores of the Li hosting anode composed of Ni particles with a gr
Herein, a freestanding cellulose acetate-carbon nanotube (CA-CNT) film electrode is presented to achieve highly flexible, high-energy lithium-ion batteries (LIBs). CA serves as a dispersing agent of CNTs and a binder-free network former. A straightforward washing can remove CA in the electrode almost completely, while the fibrous CNT network within the electrode is sustained. Furthermore, the facile fabrication enables the large-scale production of the film electrode because the CA-CNT film is p
Abstract The alloying behavior of Li‐alloy‐forming metals in the anode of all‐solid‐state batteries (ASSBs) critically affects the viscoplastic flow and deposition of Li, determining cell performance. Herein, an ultra‐stable breathing Mg anode for Li‐free ASSBs is reported with changes in the inter‐particle distance of the Mg particles during operation. It is proposed that this unique Li deposition between Mg particles is derived from the Li concentration gradient (LCG) from the surface to the c