Chang Won Yoon
경희대학교 Materials Science · 재료과학
이 교수의 연구실은 주로 수소 저장 및 수소 방출을 위한 고체 상태의 화학적 수소 저장 재료 개발에 초점을 맞추고 있습니다. 특히 페로티드 나노입자 기반 촉매를 활용한 포름산에서의 수소 생성 반응과 암모니아 트라이보란과 같은 새로운 수소 저장 물질의 합성 및 안정성, 해리 거시학적 특성에 대한 연구를 진행하고 있습니다. 메세포러스 실리카, 탄소 질화물 등 고도로 구조화된 고체 기초 촉매를 활용해 효율적이고 안정적인 수소 공급 체계를 구축하는 데 목적이 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Reversible, carbon dioxide mediated chemical hydrogen storage was first demonstrated using a heterogeneous Pd catalyst supported on mesoporous graphitic carbon nitride (Pd/mpg-C3N4). The Pd nanoparticles were found to be uniformly dispersed onto mpg-C3N4 with an average size of 1.7 nm without any agglomeration and further exhibit superior activity for the dehydrogenation of formic acid with a turnover frequency of 144 h−1 even in the absence of external bases at room temperature. Initial DFT stu
A convenient and safe method for the synthesis of ammonia triborane is reported along with studies of its hydrolytic reactions that demonstrate ammonia triborane is both soluble and stable in water but that upon the addition of acid or an appropriate transition metal catalyst it rapidly releases hydrogen. These studies indicate that ammonia triborane is a promising material for chemical hydrogen storage applications.
Amine-functionalized mesoporous silica-supported ultrasmall Pd nanoparticles catalyze hydrogen evolution from formic acid at ambient temperature.
The Ti-based heterogeneous catalysts TiSBA15, BucapTiSBA15, TS-1, and [Ti,Al]-MFI were investigated with respect to controlling factors for the competitive decomposition of aqueous H2O2 during selective catalytic oxidations. DRUV–vis spectroscopy revealed that the titanium species in these materials exist mainly in isolated, tetrahedral coordination environments. The observed rates of H2O2 decomposition at 65 °C in acetonitrile decreased in the following order: BucapTiSBA15 > TiSBA15 and TS-1 >
A series of Pd/SBA-15-amine materials (where “Amine” is primary amine, secondary amine and tertiary amine) containing Pd nanoparticles are synthesized and their catalytic properties for formic acid dehydrogenation are investigated.
Iodine oxidation of B(3)H(8)(-) in glyme solution to produce (glyme)B(3)H(7), followed by displacement of the coordinated glyme by reaction with anhydrous ammonia provides a safe and convenient preparation of ammonia triborane, NH(3)B(3)H(7) (1). X-ray crystallographic determinations and DFT computational studies of both NH(3)B(3)H(7) and the NH(3)B(3)H(7) x 18-crown-6 adduct demonstrate that while computations predict a symmetric single bridging-hydrogen conformation, NH(3)B(3)H(7) has a highly
Hydrogen storage in the form of a liquid chemical is an important issue that can bridge the gap between sustainable hydrogen production and utilization with a fuel cell, which is one of the essential sectors in the hydrogen economy. Herein, the application of a potential liquid organic hydrogen carrier, consisting of biphenyl and diphenylmethane, is demonstrated as a safe and economical hydrogen storage material. The presented material is capable of a reversible storage and release of molecular
Exfoliated graphitic carbon nitride nanosheets (g-C3N4-NS) were applied for the first time for the preparation of an electrocatalyst for the oxygen reduction reaction (ORR). A less dense structure with increased surface area was observed for g-C3N4-NS compared to bulk g-C3N4 from detailed analyses including TEM, STEM, AFM with depth profiling, XRD, and UV-Vis spectroscopy. The pyrolysis of the prepared g-C3N4-NS with Co and carbon under an inert environment provided an enhanced accessibility to
