Chang Won Yoon
Pohang University of Science and Technology · 材料科学
研究室紹介
Professor Chang Won Yoon's research lab specializes in the development of advanced nanomaterials and heterogeneous catalysts for sustainable energy applications, with a primary focus on chemical hydrogen storage and hydrogen release. The lab investigates novel materials such as Pd nanoparticles supported on carbon nitride and mesoporous silica, as well as borane-based compounds like ammonia triborane, to enable efficient, ambient-condition hydrogen generation from formic acid and other hydrogen carriers. Key research directions include understanding the role of surface basicity, metal-support interactions, and molecular-level mechanisms through combined experimental and DFT computational studies. The lab also explores the stability and reactivity of boron-nitrogen hydrides in aqueous and biphasic environments for safe and controllable hydrogen delivery.
Research Overview
Research Output Trend
Figures are computed from collected data and may differ slightly.
Selected Papers
15Reversible, 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, Bu cap TiSBA15, TS-1, and [Ti,Al]-MFI were investigated with respect to controlling factors for the competitive decomposition of aqueous H 2 O 2 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 H 2 O 2 decomposition at 65 °C in acetonitrile decreased in the following order: Bu cap TiSBA15 > TiSBA15 a
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