Korea University · Energy
Kwangyeol Lee 교수의 연구실은 에너지 전환 및 저장 기술을 위한 첨단 나노소재 개발에 초점을 맞추고 있습니다. 특히 MXene 계열 소재, 희토류 금속을 포함한 다금속 나노구조 촉매, 그리고 전기화학적 반응(예: 수소 생산, 이산화탄소 환원)에 활용 가능한 저비용·고성능 촉매의 설계 및 기초 메커니즘 규명을 주요 연구 방향으로 삼고 있습니다. 나노구조의 형태 제어, 표면 화학적 특성 조절, 그리고 반응 조건에서의 활성 상황 분석을 통해 실용적이고 지속 가능한 에너지 시스템의 핵심 소재를 창출하고자 합니다.
Figures are computed from collected data and may differ slightly.
This review addresses the recent developments and progress in the synthesis, structure and properties of MXenes, as well as their energy conversion and storage and related applications.
Highly efficient and low-cost electrocatalysts are essential for water spitting via electrolysis in an economically viable fashion. However, the best catalytic performance is found with noble metal-based electrocatalysts, which presents a formidable obstacle for the commercial success of electrolytic water splitting-based H<sub>2</sub> production due to their relatively high cost and scarcity. Therefore, the development of alternative inexpensive earth-abundant electrode materials with excellent
Thermal decomposition of W(CO)6 in oleylamine in the presence of mild oxidant Me3NO·2H2O produces tungsten oxide nanorods with diameters ranging from 3 to 6 nm. The size of nanorods can be easily varied by the employed surfactant ratio or reaction temperature. The prepared tungsten oxide nanorods exhibit strong photoluminescence (PL) peaks in 300−500 nm, which show a weak size dependency.
Electrochemical reduction of carbon dioxide (CO<sub>2</sub> RR) product distribution has been identified to be dependent on various surface factors, including the Cu facet, morphology, chemical states, doping, etc., which can alter the binding strength of key intermediates such as *CO and *OCCO during reduction. Therefore, in-depth knowledge of the Cu catalyst surface and identification of the active species under reaction conditions aid in designing efficient Cu-based electrocatalysts. This pro
While the realization of clean and sustainable energy conversion systems primarily requires the development of highly efficient catalysts, one of the main issues had been designing the structure of the catalysts to fulfill minimum cost as well as maximum performance. Until now, noble metal-based nanocatalysts had shown outstanding performances toward the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER). However, the scarcity and high cost of
Development of oxygen evolution reaction (OER) catalysts with reduced precious metal content while enhancing catalytic performance has been of pivotal importance in cost‐effective design of acid polymer electrolyte membrane water electrolyzers. Hollow multimetallic nanostructures with well‐defined facets are ideally suited for saving the usage of expensive precious metals as well as boosting catalytic performances; however, Ir‐based hollow nanocatalysts have rarely been reported. Here, a very si
Critical assessment of the present status of HEA NPs as catalysts, including an in-depth discussion of computational studies, combinatorial screening, or machine-learning studies to find the optimum composition and structure of HEA electrocatalysts.
Abstract Noble metal binary alloy nanoframes have emerged as a new class of fuel cell electrocatalysts because of their intrinsic high catalytic surface area and accompanied high catalytic activity. However, their inferior structural and compositional stability during catalysis pose as formidable huddles to their practical applications. Herein, it is reported that introduction of an additional component to the binary catalytic system may serve as a simple and effective means of enhancing the str
[60]Fullerene can bind a variety of metal clusters via eta(2)-C(60), mu-eta(2):eta(2)-C(60), and mu(3)-eta(2):eta(2):eta(2)-C(60) pi-type bonding modes. Multiple C(60) additions to a single cluster core have also been demonstrated. Modification of the coordination sphere of cluster moieties has resulted in novel transformation of the coordination mode of the C(60) ligand between pi and sigma (mu(3)-eta(1):eta(1):eta(2)-C(60) and mu(3)-eta(1):eta(2):eta(1)-C(60)) types as well as reversible inter
Nanoframe alloy structures represent a class of high-performance catalysts for the oxygen reduction reaction (ORR), owing to their high active surface area, efficient molecular accessibility, and nanoconfinement effect. However, structural and chemical instabilities of nanoframes remain an important challenge. Here, we report the synthesis of PtCu nanoframes constructed with an atomically ordered intermetallic structure (<i>O</i>-PtCuNF/C) showing high ORR activity, durability, and chemical stab
This article reviews recent advances in the synthetic strategies for metal/metal compound hetero-interfaces within a nanostructure and their beneficial synergistic effect on the electrocatalytic performance toward energy conversion applications such as the HER, OER and ORR.
This review critically assessed the progress of hybrid LDHs nanostructure as competent multifunctional nanomaterials for energy conversion and storage systems.
The catalytic properties of nanoparticles are determined by the nature of nanoparticle surface. Thus facet-controlled synthesis of catalytic nanoparticles is of paramount importance for both reactive and selective catalysis, and recently various successful synthetic methodologies have been developed to give a number of facet-controlled nanoparticles. In this review, we highlight these recent developments in facet-controlled nanoparticle synthesis along with novel strategies to enhance nanopartic
The rational design of highly efficient electrocatalysts for the hydrogen evolution reaction (HER) is of prime importance for establishing renewable and sustainable energy systems. The alkaline HER is particularly challenging as it involves a two-step reaction of water dissociation and hydrogen recombination, for which platinum-based binary catalysts have shown promising activity. In this work, we synthesized high performance platinum-nickel-cobalt alloy nanocatalysts for the alkaline HER throug
Image enhancement: Core–shell [email protected]3O4 urchin-shaped nanoparticles can be synthesized by means of an anisotropic etching process and used as a pH-activatable T1 contrast agent for magnetic resonance imaging. The manganese ions released from the MnO phase in the low-pH sites within tumor cells lead to an enhanced T1 contrast image for the entire tumor mass. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, b
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