Korea Advanced Institute of Science and Technology · Energy
오지훈 교수의 연구실은 태양 에너지 변환 및 전기화학적 반응을 위한 나노구조 소재 개발에 초점을 맞추고 있습니다. 특히 실리콘 기반 광전극을 활용한 수소 생산, CO₂ 전환 반응의 효율성 향상, 그리고 고성능 나노촉매를 통한 유기물 전환 반응 등 에너지 전환과 환경 문제 해결을 위한 혁신적 기술을 연구하고 있습니다. 다양한 나노구조 설계와 표면 제어 기반의 촉매 및 전극 설계가 핵심 기술입니다.
Figures are computed from collected data and may differ slightly.
Nanostructured Si eliminates several critical problems with Si photocathodes and dramatically improves a photoelectrochemical (PEC) reaction important to water-splitting. Our nanostructured black Si photocathodes improve the H2 production by providing (1) near-ideal anti-reflection that enables the absorption of most incident light and its conversion to photogenerated electrons and (2) extremely high surface area in direct contact with water that reduces the overpotential needed for the PEC hydr
Electrocatalytic CO<sub>2</sub> reduction is a promising way to provide renewable energy from gaseous CO<sub>2</sub> The development of nanostructures improves energy efficiency and selectivity for value-added chemicals, but complex nanostructures limit the CO<sub>2</sub> conversion rates due to poor mass transport during vigorous electrolysis. Herein, we propose a three-dimensional (3D) hierarchically porous Au comprising interconnected macroporous channels (200-300 nm) and nanopores (∼10 nm) f
Converting solar energy by photoelectrochemical water splitting has been regarded as a promising way to resolve the global energy crisis and alleviate environmental pollution. Silicon, which is earth-abundant and has a narrow band gap, is an attractive material for photoelectrochemical water splitting. However, Si-based photoelectrodes suffer from photocorrosion, which leads to instability in electrolytes and high overpotential. Herein, we have fabricated a metal–insulator–semiconductor structur
Abstract This study reports on substantial improvement of the open‐circuit voltage ( V oc ) of Cu 2 ZnSnSe 4 (CZTSe) thin film solar cells by applying a passivation strategy to both the top and bottom interfaces of the CZTSe absorber, which involves insertion of a thin dielectric layer between the CZTSe and the surrounding layers. The study also presents in‐depth material characterizations using transmission electron microscopy, energy dispersive X‐ray spectroscopy, low‐temperature photoluminesc
Morphology-controlled Au nanostructures are fabricated<italic>via</italic>electroreduction of anodized Au thin films, exhibiting efficient catalytic activity for electrochemical CO<sub>2</sub>reduction.
The glycerol electro-oxidation reaction (GEOR) can economically convert glycerol, a byproduct of biodiesel production, to glycolic acid. Herein, nanostructured Au catalysts were fabricated on a Si substrate by the electrochemical reduction of anodic-treated (RA-treatment) Au films, which tuned the surface area from 1 to 16 cm2. Treatment of 0.1 M glycerol at 1.0 V (vs RHE) for 2 h in 1 M KOH solution afforded a glycerol conversion and glycolic acid selectivity of 50.9 and 47%, respectively. The
Cu acetate/PAN nanofibers were transformed into porous C nanofibers with doped N and Cu particles,<italic>via</italic>O<sub>2</sub>partial pressure-controlled calcination. N atoms next to Cu trigger the CO<sub>2</sub>RR by increasing the amount of CO* on the Cu, lowering the energy needed for CO dimerization.
The effect of local atomic arrangement of CuZn alloys was demonstrated on enhanced ethanol selectivity from CO 2 RR and supported by density functional theory (DFT) calculations.
The evaluation of catalysts on gas diffusion electrodes (GDEs) have propelled the progress of electrochemical CO2 reduction reaction (CO2RR) at industry-relevant activities. However, high experimental complexities exist in GDE-based flow electrolyzers, whereby various experimental factors can influence the evaluation of catalytic CO2RR performances. Not accounting for these experimental factors could result in inconsistent conclusions and thus hinder rational catalyst developments. This Perspect
A Ni single-atom catalyst with Ni–N4–xCx active sites is prepared in a single pyrolysis step in which the Ni single atom is incorporated in the carbon framework through nitrogen and carbon coordination utilizing the ionothermal synthesis method. In comparison to the complicated synthesis procedures of single-atom catalysts, this method provides a general and facile method to obtain single-atom catalysts with an opportunity to synthesize catalysts at a large scale. The precursors used in this met
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