Hitoshi Ogihara

ORCID: 0000-0003-0623-664X
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Research Areas
  • Catalytic Processes in Materials Science
  • Electrocatalysts for Energy Conversion
  • Catalysis and Oxidation Reactions
  • Catalysts for Methane Reforming
  • Surface Modification and Superhydrophobicity
  • CO2 Reduction Techniques and Catalysts
  • Advanced battery technologies research
  • Zeolite Catalysis and Synthesis
  • Carbon Nanotubes in Composites
  • Electrodeposition and Electroless Coatings
  • Carbon dioxide utilization in catalysis
  • Electrophoretic Deposition in Materials Science
  • Fuel Cells and Related Materials
  • Ammonia Synthesis and Nitrogen Reduction
  • Supercapacitor Materials and Fabrication
  • Hybrid Renewable Energy Systems
  • Aerosol Filtration and Electrostatic Precipitation
  • Ionic liquids properties and applications
  • Transition Metal Oxide Nanomaterials
  • Graphene research and applications
  • Semiconductor materials and interfaces
  • Hydrogen Storage and Materials
  • Nanowire Synthesis and Applications
  • Catalysis and Hydrodesulfurization Studies
  • TiO2 Photocatalysis and Solar Cells

Saitama University
2018-2024

Tokyo Institute of Technology
2010-2020

Department of Chemistry and Material Sciences
2015

Hokkaido University
2006-2011

Japan Society for the Promotion of Science
2006-2009

Superhydrophobic and transparent coatings are deposited onto paper by spraying alcohol suspensions of SiO(2) nanoparticles. Superhydrophobicity depends on the aggregation states nanoparticles, which determined type used in suspensions. The superhydrophobicity is maintained after touching with a bare finger.

10.1021/la204492q article EN Langmuir 2012-02-27

10.1016/j.colsurfa.2013.05.034 article EN Colloids and Surfaces A Physicochemical and Engineering Aspects 2013-05-16

Superhydrophobic coatings were prepared by spraying a pigment nanoparticle suspension. By changing the type of nanoparticles, colors coating could be controlled. The particle size pigments, which determines surface structure coatings, played an important role in exhibiting superhydrophobicity. spray-coating process is applicable to variety materials (e.g., copper, glass, paper, coiled wire, and tied thread), superhydrophobicity was repairable.

10.1021/la200898z article EN Langmuir 2011-07-01

An organic hydride system based on hydrogenation/dehydrogenation of toluene (TL)/methylcyclohexane (MCH) has been studied as a hydrogen storage technology. Electrohydrogenation TL to MCH using proton exchange membrane (PEM) electrolyzer is proposed candidate for the hydrogenation in system. Recently, we reported that Ketjenblack-supported Ru-Ir alloy (Ru-Ir/KB) cathode was effective reaction; however, electrohydrogenation mechanisms and catalyses Ru Ir have unclear. In this paper, detailed...

10.1021/acscatal.8b03610 article EN ACS Catalysis 2019-02-15

Shape-controlled fabrication process for oxide nanotubes (ZrO2, Al2O3, and SiO2) by using carbon nanofibers templates was developed. By thick, thin, coiled as templates, shapes of could be controlled, that is, a variety attractive nanotubular materials synthesized.

10.1021/cm061266t article EN Chemistry of Materials 2006-09-20

The direct dehydrogenative conversion of methane (DCM) to higher hydrocarbons has attracted much attention, because the efficient utilization natural gas. Ni catalysis activation C–H bonds H2 and C is well-known. We have tried control via addition second elements found silica-supported nickel phosphide (Ni–P/SiO2) materials as active catalysts for DCM reaction at 1173 K. products included C2H4 (ethylene), C2H6 (ethane), C2H2 (acetylene), C3H6 (propylene), C6H6 (benzene), C7H8 (toluene),...

10.1021/acscatal.9b03955 article EN ACS Catalysis 2019-12-05

Abstract Three-dimensionally ordered macroporous (3DOM) materials of spinel-type MFe2O4 (M = Zn, Ni, ZnxNi1−x (x 0.2–0.8), and Co) mixed iron oxides were prepared in excellent yields by using a colloidal crystal templating method. Mixed metal nitrates dissolved an ethylene glycol (EG)–methanol solvent penetrated into the void template poly(methyl methacrylate) (PMMA) spheres. During calcination process, reacted with converted glyoxylate derivatives voids crystals before polymer sphere was...

10.1246/bcsj.80.677 article EN Bulletin of the Chemical Society of Japan 2007-04-01

Abstract Catalysts for dehydrogenative conversion of methane (DCM) to higher hydrocarbons are worthy attention. Indium supported on silica (In/SiO 2 ) was found effective catalyst the DCM reaction above 1023 K. Products were ethane, ethylene, acetylene, propylene, benzene, toluene, naphthalene and hydrogen. A highest selectivity sum products 96 % at 1098 K a steady‐state yield 2.1 with 63 1173 Characterization studies using temperature‐programed X‐ray diffraction (TP‐XRD) scanning electron...

10.1002/slct.201700734 article EN ChemistrySelect 2017-05-31

Methyl formate (MF) is an important intermediate in the production of essential chemicals such as formic acid chemical industry. Although MF currently synthesized via liquid-phase carbonylation methanol, this process has certain problems (e.g., catalyst deactivation). In regard, alternative processes for have been extensively examined, and formation with a high selectivity rate at mild reaction conditions remains critical goal research. Here, we demonstrated synthesis direct electrolysis...

10.1021/acssuschemeng.0c02281 article EN ACS Sustainable Chemistry & Engineering 2020-07-14

Inert CH<sub>4</sub> molecules can be activated and incorporated into pyrolysis products with the aid of radicals generated by C<sub>2</sub>H<sub>6</sub>.

10.1039/c9re00400a article EN Reaction Chemistry & Engineering 2019-11-14

Abstract Dry reforming of methane (DRM) is a promising catalytic process for converting greenhouse gases (CH 4 and CO 2 ) into syngas (CO H ). This study investigates DRM under moderate conditions (550 °C) using supported low‐loading (0.05 wt%) metal (M) catalysts (M = Rh, Ru, Pt, Pd, Ir, Au, Ni). The reaction was carried out 6 h with flow rate 30 mL/min both CH , 0.10 g catalyst. Among these catalysts, 0.05 wt% Rh/Al O 3 exhibited the highest activity. effect catalyst supports revealed that...

10.1002/cctc.202401386 article EN cc-by ChemCatChem 2024-11-06

SiO2 nanotubes could be synthesized by hydrolysis of tetraethyl orthosilicate (TEOS) on the surface carbon nanofibers (CNF), followed removal CNF. In synthesis nanotubes, CNF acted as templates. The wall thickness and internal diameter were changed time TEOS templates, respectively. catalysts for functional groups methane decomposition was carried out over containing Ni metal particles, so that with uniform (ca. 8 nm) formed at inside nanotubes. This result strongly indicated worked...

10.1021/cm051727v article EN Chemistry of Materials 2006-01-19

The hydrogen evolution reaction (HER) was carried out over Ni nanospike arrays prepared by electroless deposition. showed higher HER activity than plates and electrodeposited because their nano-sized roughness results in a high surface area.

10.1039/c4ra11646a article EN cc-by RSC Advances 2014-10-23

The direct acetalization of ethanol is a significant challenge for upgrading bioethanol to value-added chemicals. In this study, 1,1-diethoxyethane (DEE) selectively synthesized by the electrolysis using proton-exchange membrane (PEM) reactor. PEM reactor, Pt/C catalyst promoted electro-oxidation acetaldehyde. Nafion used as served solid acid and electrochemically formed DEE was obtained at high faradaic efficiency (78 %) through sequential electrochemical nonelectrochemical reactions....

10.1002/cssc.202101188 article EN ChemSusChem 2021-07-22

Electrochemical water splitting is a key technology for the conversion of renewable energy into chemical resources such as hydrogen. However, oxygen evolution reaction (OER), half-reaction splitting, so slow that various effective catalysts OER have been explored. In this study, we demonstrate simple and direct process synthesis OER-active NiFe over electrodes. A NiFe/C catalyst layer was formed on glassy carbon electrode by simply dropping ink containing only metal nitrates black. The...

10.1021/acs.langmuir.2c00097 article EN Langmuir 2022-04-29
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