京都大学 · Energy
류 아베 교수의 연구실은 태양광을 이용한 수소 생산을 핵심 목표로 하며, 저비용이고 내구성이 뛰어난 반도체 광촉매를 활용한 물 분해 기반 청정 에너지 기술을 연구하고 있습니다. 특히 Z-스키마 시스템, 이온 산화환원 매개체를 활용한 이중 광촉매 반응체계, 그리고 TaON, Ta₃N₅ 등의 산화질화물 기반 전극을 활용한 고효율 수분해 시스템 개발에 주력하고 있습니다. 광촉매의 표면 촉매화 및 전하 수송 효율을 극대화하기 위한 나노입자 도핑 및 접합 기술도 핵심 연구 요소입니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Visible light-driven water splitting using cheap and robust photocatalysts is one of the most exciting ways to produce clean and renewable energy for future generations. Cutting edge research within the field focuses on so-called "Z-scheme" systems, which are inspired by the photosystem II-photosystem I (PSII/PSI) coupling from natural photosynthesis. A Z-scheme system comprises two photocatalysts and generates two sets of charge carriers, splitting water into its constituent parts, hydrogen and
Tungsten oxide loaded with nanoparticulate platinum is demonstrated to exhibit high activity for the decomposition of organic compounds both in liquid and gas phases; the activity was almost comparable to that of TiO2 under UV light irradiation and much higher than that of nitrogen-doped TiO2 under visible irradiation.
The porous oxynitride TaON film electrode prepared on conducting glass (FTO) showed significantly high quantum efficiency (IPCE = ca. 76% at 400 nm at 0.6 V vs Ag/AgCl) in an aqueous Na(2)SO(4) solution, after loading of IrO(2) x nH(2)O nanoparticles as a cocatalyst for water oxidation. Overall water splitting into H(2) and O(2) under visible light was demonstrated using an IrO(2) x nH(2)O-loaded TaON photoanode combined with a Pt electrode under an externally applied bias (0.6-1 V).
A new type of photocatalytic reaction that splits water into H2 and O2 was designed using a two-step photoexcitation system composed of an iodate/iodide (IO3-/I-) shuttle redox mediator and two different photocatalysts, one for H2 evolution and the other for O2 evolution. Photocatalytic oxidation of water to O2 and reduction of IO3- to I- selectively proceeded with good efficiencies over TiO2-rutile and Pt-WO3 photocatalysts under UV and visible light irradiations, respectively. The O2 evolution
Efficient TaON and Ta3N5 photoanodes for water splitting were fabricated on conducting glass support (FTO). A necking treatment, which forms effective contacts between TaON (or Ta3N5) particles, afforded a significant increase in the photocurrent. Furthermore, loading of IrO2·nH2O nanoparticles as a cocatalyst for water oxidation improved the photocurrent of the TaON (or Ta3N5) photoanode. The incident photon to charge carrier efficiencies (IPCEs) of the TaON and Ta3N5 photoanodes were calculate
Photocatalytic water splitting into H2 and O2 under visible-light irradiation (lambda > 420 nm) is demonstrated using the oxynitride Pt-TaON for H2 evolution and a Pt-WO3 catalyst for O2 evolution in an IO3-/I- shuttle redox-mediated system.
The photocatalytic activities of R3MO7 and R2Ti2O7 (R=Y, Gd, La; M=Nb, Ta) strongly depended on the crystal structure. Overall, photocatalytic water splitting into H2 and O2 proceeded over La3TaO7 and La3NbO7, which have an orthorhombic weberite structure, Y2Ti2O7 and Gd2Ti2O7, which have a cubic pyrochlore structure, and La2Ti2O7, which has a monoclinic perovskite structure. All of these materials are composed of a network of corner-shared octahedral units of metal cations (TaO6, NbO6, or TiO6)
Water splitting into H2 and O2 under visible light was achieved using simple organic dyes such as coumarin and carbazole as photosensitizers on an n-type semiconductor for H2 evolution, a tungsten(VI) oxide (WO3) photocatalyst for O2 evolution, and a triiodide/iodide (I3(-)/I(-)) redox couple as a shuttle electron mediator between them. The results on electrochemical measurements revealed that the oxidized states of the dye molecules having an oligothiophene moiety (two or more thiophene rings)
Photocatalytic splitting of water into H(2) and O(2) under visible light irradiation is achieved using a coumarin-dye-adsorbed lamellar niobium oxide for hydrogen evolution.
Abstract Photocatalytic water splitting using semiconductor materials has attracted considerable interest due to its potential for clean production of H2 from water by utilizing abundant solar light. The developments of water-splitting systems that can efficiently use visible light have been a major challenge for many years in order to realize efficient conversion of solar light. We have developed a new type of photocatalysis system that can split water into H2 and O2 under visible light irradia
Three-dimensionally ordered macroporous (3DOM) tungsten(VI) oxide (WO3) was prepared using a colloidal crystal template method. Well-ordered 3DOM WO3 was prepared with a high pore fraction using ammonium metatungstate ((NH4)6H2W12O40), a Keggin-type dodecatungstate, as a tungsten precursor; WO3 materials prepared by other commercially available W precursors, tungsten chloride (WCl6), tungsten(V) ethoxide (W(OEt)5), and phosphotungstic acid (H3PW12O40), have a low 3DOM pore fraction. These WO3 ma