한성환 교수
Sung‐Hwan Han
한양대학교 화학과 · 재료과학
연구실 소개
한성환 교수의 연구실은 나노소재 합성과 에너지 변환·저장 기술을 중심으로 활발한 연구를 수행하고 있습니다. 특히 이산화탄소를 메탄올로 전환하는 카본 캡처 및 활용 기술(CAMERE 공정), 광반응성 나노구조체(티타니아, 카드뮴 sulfide 등)의 저온 합성 및 헤테로구조 형성, 전기화학적 방법을 통한 나노결정성 산화锡 전극 개발 등이 주요 연구 분야입니다. 또한 알츠하이머병 조기 진단을 위한 고감도 다가성 펩타이드 프로브 개발을 통해 바이오센서 기술과의 융합도 시도하고 있습니다.
연구 현황
연구 성과 추이
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주요 논문
15The CAMERE process (carbon dioxide hydrogenation to form methanol via a reverse-water-gas-shift reaction) was developed and evaluated. The reverse-water-gas-shift reactor and the methanol synthesis reactor were serially aligned to form methanol from CO 2 hydrogenation. Carbon dioxide was converted to CO and water by the reverse-water-gas-shift reaction (RWReaction) to remove water before methanol was synthesized. With the elimination of water by RWReaction, the purge gas volume was minimized as
Synthesis of TiO 2 nanowires directly on conductive and transparent glass substrates would be very useful for various applications such as photovoltaics and photocatalysis. Here, we report for the first time that single-crystalline TiO 2 nanowires can be synthesized on fluorine-doped tin oxide (SnO 2:F)-coated soda-lime glass substrates by chemical vapor deposition (CVD) at a temperature that is below the glass softening temperature (<530 °C). Moreover, we demonstrate that CdS nanorods with high
1-D array of Co<sub>3</sub>[Fe(CN)<sub>6</sub>]<sub>2</sub> film obtained by ion exchange mediated chemical transformation route from Co(CO<sub>3</sub>)<sub>0.35</sub>Cl<sub>0.20</sub>(OH)<sub>1.10</sub> demonstrated an enhanced electrocatalytic oxidation of alkaline and neutral water.
High-density and single-crystalline CdS nanowire arrays were formed on fluorine-doped tin oxide (FTO)-coated soda-lime glass substrates without aid of templates at 220 °C. Bi was employed as a catalyst for the low-temperature growth of CdS nanowires via solution−liquid−solid (SLS) mechanism. CdS nanowires were very straight and they were ∼20−50 nm in diameter and ∼2−3 μm in length. CdS nanowires were in highly crystalline wurtzite structure, and their crystal growth direction was [001]. Careful
The present article demonstrates the use of low-cost electrochemically synthesized hydrophilic and nanocrystalline tin oxide film electrodes at room temperature in dye-sensitized solar cells and electrochemical supercapacitors. A mixed phase of tin instead of single phase composed of uniformly distributed irregular spherical grains in a nanometer regime scale was obtained. Tin oxide film electrode showed efficient photoperformance when subjected to dye-sensitized solar cells. The interfacial and
Amyloid-beta 42 (Aβ<sub>42</sub>), the key biomarker of Alzheimer's disease (AD), aggregates to form neurotoxic amyloid plaques. In this work, we modified two fluorescein isothiocyanate-labeled Aβ<sub>42</sub>-targeting peptides and designed an Aβ<sub>42</sub>-specific ultrasensitive polyvalent-directed peptide polymer (PDPP) to enhance AD diagnosis sensitivity. The dissociation constant of Aβ<sub>42</sub> by PDPP was 10<sup>3</sup>-fold higher than the single-site-directed peptide. The improved
High-density and single-crystalline CdS nanowires were grown on fluorine-doped tin oxide (FTO)/soda-lime glass substrates using Bi catalysts via the so-called solution−liquid−solid (SLS) mechanism. Through a series of voltage loading steps, high-quality Cu(In,Ga)Se 2 (CIGS) light absorption layers were electrochemically deposited on the CdS window layers and subsequently selenized at 400 °C to form photovoltaic cells. Due to the one dimensionality and single crystallinity of the CdS nanowires, t
In order to enhance the capacitance of electrochemical capacitors, multiwalled carbon nanotubes (MWCNTs) and graphene nanosheets (GNS) were added to cobalt oxide (Co3O4) paste. The composite film based on Co3O4/MWCNT/GNS (95:4:1 wt%) exhibited a capacitance of 294 F/g while the capacitance of Co3O4/MWCNT (95:5 wt%) and pure Co3O4 film is 205 and 163 F/g, respectively. The enhanced capacitance of Co3O4/MWCNT/GNS composite film was attributed to the electrochemical contributions of the Co3O4 nanop
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