Jinwoo Lee 교수

Abstract In this review, the progress made in the last ten years concerning the synthesis of porous carbon materials is summarized. Porous carbon materials with various pore sizes and pore structures have been synthesized using several different routes. Microporous activated carbons have been synthesized through the activation process. Ordered microporous carbon materials have been synthesized using zeolites as templates. Mesoporous carbons with a disordered pore structure have been synthesized

A correct alignment is an essential requirement in homology modeling. Yet in order to bridge the structural gap between template and target, which may not only involve loop rearrangements, but also shifts of secondary structure elements and repacking of core residues, high-resolution refinement methods with full atomic details are needed. Here, we describe four approaches that address this "last mile of the protein folding problem" and have performed well during CASP8, yielding physically realis

A mesoporous carbon with regular three-dimensionally interconnected 2 nm pore arrays using AlMCM-48 as a template has been synthesised; the mesoporous carbon exhibited excellent performance as an electrochemical double layer capacitor.

Replacement of Pt-based oxygen reduction reaction (ORR) catalysts with non-precious metal catalysts (NPMCs) such as Fe/N/C is one of the most important issues in the commercialization of proton exchange membrane fuel cells (PEMFCs). Despite numerous studies on Fe/N/C catalysts, a fundamental study on the development of a versatile strategy is still required for tuning the kinetic activity of a single Fe-N4 site. Herein, we report a new and intuitive design strategy for tuning and enhancing the k

Abstract Lithium–sulfur batteries (LSBs) are cost‐effective and high‐energy‐density batteries. However, the insulating nature of active materials, the shuttle effect, and slow redox kinetics lead to severe capacity decay and low rate capabilities. Numerous multimodal approaches have been attempted to tackle these issues and have pushed the cycle stability and energy density to higher levels. Recently, accelerating the redox kinetics using catalytic materials has been considered as a means to rea

Single-atom catalysts (SACs) have attracted growing attention because they maximize the number of active sites, with unpredictable catalytic activity. Despite numerous studies on SACs, there is little research on the support, which is essential to understanding SAC. Herein, we systematically investigated the influence of the support on the performance of the SAC by comparing with single-atom Pt supported on carbon (Pt SA/C) and Pt nanoparticles supported on WO_3-x (Pt NP/WO<sub>3-x</su

Sodium‐ion hybrid supercapacitors (Na‐HSCs) have potential for mid‐ to large‐scale energy storage applications because of their high energy/power densities, long cycle life, and the low cost of sodium. However, one of the obstacles to developing Na‐HSCs is the imbalance of kinetics from different charge storage mechanisms between the sluggish faradaic anode and the rapid non‐faradaic capacitive cathode. Thus, to develop high‐power Na‐HSC anode materials, this paper presents the facile synthesis

In this review, we summarize recent reports on the synthesis of various nanoporous carbon materials. Many nanoporous carbon materials having variable pore sizes and pore structures have been synthesized using appropriate nanostructured silica materials as templates. Nanoporous carbons with high pore volumes and uniform pore sizes have been produced using silica sol and silica gel as templates. Mesoporous carbons with several different pore structures have been synthesized using mesoporous silica

Mesoporous carbon materials are desirable electrode materials and are also useful for the separation of bulky organics. In this article, the templated synthesis of a new high surface area mesoporous carbon using hexagonal mesoporous silica (HMS) aluminosilicate is reported. Preliminary results on the electrochemical double-layer capacitance performance of the material are presented that indicate that it is superior to the commercially available carbon MSC-25. In addition, the pore structure of H

Uniformly sized silica-coated magnetic nanoparticles (magnetite@silica) are synthesized in a simple one-pot process using reverse micelles as nanoreactors. The core diameter of the magnetic nanoparticles is easily controlled by adjusting the w value ([polar solvent]/[surfactant]) in the reverse-micelle solution, and the thickness of the silica shell is easily controlled by varying the amount of tetraethyl orthosilicate added after the synthesis of the magnetite cores. Several grams of monodisper

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTFabrication of Novel Mesocellular Carbon Foams with Uniform Ultralarge MesoporesJinwoo Lee, Kwonnam Sohn, and Taeghwan HyeonView Author Information School of Chemical Engineering and Institute of Chemical Processes Seoul National University, Seoul 151-742, Korea Cite this: J. Am. Chem. Soc. 2001, 123, 21, 5146–5147Publication Date (Web):May 4, 2001Publication History Received5 January 2001Revised13 April 2001Published online4 May 2001Published in

In recent years, porous materials have attracted significant attention in various research fields because of their structural merits. In particular, well-designed mesoporous structures with two- or three-dimensionally interconnected pores have been recognized as electrode materials of particular interest for achieving high-performance electrochemical capacitors (ECs). In this mini review, recent progress in the design of mesoporous electrode materials for ECs, from electric double-layer capacito

Abstract Over the past decade, the catalytic activity of nanozymes has been greatly enhanced, but their selectivity is still low and considered a critical issue to overcome. Herein, Fe–N 4 single site embedded graphene (Fe–N‐rGO), which resembles the heme cofactor present in natural horseradish peroxidase, shows a marked enhancement in peroxidase‐like catalytic efficiency of up to ≈700‐fold higher than that of undoped rGO as well as excellent selectivity toward target H 2 O 2 without any oxidizi