Hokkaido University · Energy
Hui Song 교수의 연구실은 태양광을 활용한 청정 에너지 변환 기술에 중점을 두고 있으며, 특히 태양광을 이용한 수소 생산, 메탄의 선택적 산화를 통한 메탄올 합성, 이산화탄소의 광촉매 환원 등 지속 가능한 연료 합성에 핵심적인 플라즈몬 나노촉매 및 광촉매 시스템을 개발하고 있습니다. 주로 나노금속과 산화물 촉매의 상호작용을 통해 열화학 반응의 활성화 에너지를 낮추고, 열화학적 반응을 광열 및 열전자 효과로 효율적으로 유도하는 기초 메커니즘을 규명하고 있습니다. 특히 실온에서 산소를 산화제로 사용하는 고선택도의 메탄 산화 반응과 CO₂의 고효율 전환 기술이 핵심 연구 과제입니다.
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Solar H2 production is considered as a potentially promising way to utilize solar energy and tackle climate change stemming from the combustion of fossil fuels. Photocatalytic, photoelectrochemical, photovoltaic–electrochemical, solar thermochemical, photothermal catalytic, and photobiological technologies are the most intensively studied routes for solar H2 production. In this Focus Review, we provide a comprehensive review of these technologies. After a brief introduction of the principles and
Direct conversion of methane into methanol and other liquid oxygenates still confronts considerable challenges in activating the first C-H bond of methane and inhibiting overoxidation. Here, we report that ZnO loaded with appropriate cocatalysts (Pt, Pd, Au, or Ag) enables direct oxidation of methane to methanol and formaldehyde in water using only molecular oxygen as the oxidant under mild light irradiation at room temperature. Up to 250 micromoles of liquid oxygenates with ∼95% selectivity is
Solar-to-fuel conversion through photocatalytic processes is regarded as promising technology with the potential to reduce reliance on dwindling reserves of fossil fuels and to support the sustainable development of our society. However, conventional semiconductor-based photocatalytic systems suffer from unsatisfactory reaction efficiencies due to limited light harvesting abilities. Recent pioneering work from several groups, including ours, has demonstrated that visible and infrared light can b
Photocatalytic reduction of carbon dioxide (CO<sub>2</sub>) is attractive for the production of valuable fuels and mitigating the influence of greenhouse gas emission. However, the extreme inertness of CO<sub>2</sub> and the sluggish kinetics of photoexcited charge carrier transfer process greatly limit the conversion efficiency of CO<sub>2</sub> photoreduction. Herein, we report that the plasmonic coupling effect of Pt and Au nanoparticles (NPs) profoundly enhances the efficiency of CO<sub>2</s
Direct and selective oxidation of CH4 with dioxygen to methanol is a "dream reaction" in modern catalysis yet remains a great challenge. Here, we report that TiO2 loaded with dual cocatalysts, that is, nanometals and cobalt oxide (CoOx) nanoclusters, is capable of selectively catalyzing CH4 to CH3OH at room temperature under photoexcitation using abundant and inexpensive O-2 as an oxidant. The best activity for the formation of the primary products, CH3OOH and CH3OH, is up to 50.8 pmol for 2 h w
Hot-carrier-induced molecular activation over photoexcited metal nanostructures is an important research field in solar-to-chemical energy conversion. Here, we report that visible light-illuminated TiO2-supported Rh nanoparticles could significantly enhance methane (CH4) activation in steam methane reforming at mild operating temperature (below 300 °C) with an ∼50% decrease in apparent activation energy compared to that of the pure thermal process. Femtosecond time-resolved infrared spectroscopi
Black TiO2 nanomaterials have attracted considerable attention since they usually exhibit excellent photocatalytic activities. Herein, we report the facile preparation of black TiO2 nanostructures with ultrathin hollow sphere morphology, high crystalline quality, small grain size (∼8 nm), and ultrahigh surface area (168.8 m2 g–1) through Al reduction. Electron paramagnetic resonance (EPR) spectra demonstrate the existence of oxygen vacancies in black TiO2 nanostructures, which could increase the
ZnFe<sub>2</sub>O<sub>4</sub>/ZnO nanoheterostructures are synthesized by a facile template method. The hydrogen generation rate of ZnFe<sub>2</sub>O<sub>4</sub>/ZnO nanoheterostructures without co-catalysts is up to 2.15 mmol h<sup>−1</sup> g<sup>−1</sup> under visible light irradiation (<italic>λ</italic> > 420 nm), which is 45 times higher than the best yields ever reported for ZnFe<sub>2</sub>O<sub>4</sub>-based photocatalysts.
Methanol steam reforming (MSR) is a promising reaction that enables efficient production and safe transportation of hydrogen, but it requires a relatively high temperature to achieve high activity, leading to large energy consumption. Here, we report a plasmonic ZnCu alloy catalyst, consisting of plasmonic Cu nanoparticles with surface-deposited Zn atoms, for efficient solar-driven MSR without additional thermal energy input. Experimental results and theoretical calculations suggest that Zn atom
Direct photocatalytic oxidation of methane to liquid oxygenated products is a sustainable strategy for methane valorization at room temperature. However, in this reaction, noble metals are generally needed to function as cocatalysts for obtaining adequate activity and selectivity. Here, we report atomically dispersed nickel anchored on a nitrogen-doped carbon/TiO<sub>2</sub> composite (Ni-NC/TiO<sub>2</sub> ) as a highly active and selective catalyst for photooxidation of CH<sub>4</sub> to C1 ox
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