Yasuhiro Shiraishi

Photocatalytic production of hydrogen peroxide (H2O2) on semiconductor catalysts with alcohol as a hydrogen source and molecular oxygen (O2) as an oxygen source is a potential method for safe H2O2 synthesis because the reaction can be carried out without the use of explosive H2/O2 mixed gases. Early reported photocatalytic systems, however, produce H2O2 with significantly low selectivity (∼1%). We found that visible light irradiation (λ > 420 nm) of graphitic carbon nitride (g-C3N4), a polymeric

Design of green, safe, and sustainable process for the synthesis of hydrogen peroxide (H2 O2 ) is a very important subject. Early reported processes, however, require hydrogen (H2 ) and palladium-based catalysts. Herein we propose a photocatalytic process for H2 O2 synthesis driven by metal-free catalysts with earth-abundant water and molecular oxygen (O2 ) as resources under sunlight irradiation (λ>400 nm). We use graphitic carbon nitride (g-C3 N4 ) containing electron-deficient aromatic diimid

Photocatalytic production of hydrogen peroxide (H2O2) from ethanol (EtOH) and molecular oxygen (O2) was carried out by visible light irradiation (λ > 420 nm) of mesoporous graphitic carbon nitride (GCN) catalysts with different surface areas prepared by silica-templated thermal polymerization of cyanamide. On these catalysts, the photoformed positive hole oxidize EtOH and the conduction band electrons localized at the 1,4-positions of the melem unit promote two-electron reduction of O2 (H2O2 for

A rhodamine-cyclen conjugate (1) behaves as a highly sensitive and selective fluorescent chemosensor for Hg(2+). The high emission selectivity is due to the formation of 1-Hg(2+) 1:2 complex leading to spirocycle opening of 1.

Titanium dioxide with a mesoporous structure, when photoactivated in water, demonstrates an unprecedented photocatalytic activity, driven strongly by an adsorption degree of molecules onto the catalyst surface, which promotes a preferential conversion of a well-adsorbed molecule. This catalyzes a selective transformation of a well-adsorbed molecule into a less-adsorbed molecule, so-labeled "stick-and-leave" transformation, which promotes a direct hydroxylation of benzene to phenol, one of the mo

A desulfurization and denitrogenation process for light oils has been investigated based on the chemical oxidation of sulfur- and nitrogen-containing compounds using hydrogen peroxide and acetic acid as oxidizing agent. Sulfur and nitrogen compounds, when dissolved in n-tetradecane and xylene, were oxidized under moderate conditions and were removed successfully. By use of this basic process, although nitrogen content of actual light oils was reduced to <22% of the corresponding feed values, sul

The generation of hydrogen peroxide (H₂O₂) from water and dioxygen by sunlight-driven heterogeneous photocatalysis is a promising method for the artificial photosynthesis of a liquid solar fuel. We previously found that resorcinol-formaldehyde (RF) resin powders prepared by high-temperature hydrothermal synthesis act as highly active semiconductor photocatalysts for H₂O₂ generation. Herein, we report that RF resin powders doped with poly(3-hexylthiophe

Dual platinum action: A one-pot catalytic synthesis of benzimidazoles from the photoirradiation of an alcohol solution containing an ortho-arylenediamine and [email protected]2 nanoparticles is described. This reaction proceeded by the platinum-assisted photocatalytic oxidation of an alcohol and a catalytic dehydrogenation of the intermediates on the surface of platinum nanoparticles. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are

Photocatalytic production of hydrogen peroxide (H2O2) on semiconductor catalysts with alcohol as a hydrogen source and molecular oxygen (O2) as an oxygen source has attracted much attention as a potential method for safe H2O2 synthesis, because the reaction can be carried out without the use of explosive H2/O2 mixed gases. Early reported photocatalytic systems with aliphatic alcohol as a hydrogen source, however, produce only a few millimolar levels of H2O2. We found that benzylic alcohols, when

Ammonia is an indispensable chemical. Photocatalytic NH₃ production via dinitrogen fixation using water by sunlight illumination under ambient conditions is a promising strategy, although previously reported catalysts show insufficient activity. Herein, we showed that ultraviolet light irradiation of a semiconductor, bismuth oxychloride with surface oxygen vacancies (BiOCl-OVs), in water containing chloride anions (Cl^-) under N₂ flow efficiently produces NH<sub>3

Visible light irradiation (λ > 450 nm) of Pt-Cu bimetallic alloy nanoparticles (~3-5 nm) supported on anatase TiO2 efficiently promotes aerobic oxidation. This is facilicated via the interband excitation of Pt atoms by visible light followed by the transfer of activated electrons to the anatase conduction band. The positive charges formed on the nanoparticles oxidize substrates, and the conduction band electrons reduce molecular oxygen, promoting photocatalytic cycles. The apparent quantum yield

A coumarin-spiropyran conjugate (2) shows a CN(-)-selective fluorescence enhancement under UV irradiation. This enables accurate determination of very low levels of CN(-) (>0.5 μM).

Rejuvenating sunlight: Supported Au–Cu bimetallic alloy nanoparticles promote aerobic oxidation at room temperature under visible light (λ>450 nm) irradiation with little deactivation by the oxidation of surface Cu atoms by oxygen. This is achieved through the reduction of oxidized surface Cu atoms by the surface Au atoms, a process which is activated by visible-light irradiation, even by sunlight. As a service to our authors and readers, this journal provides supporting information supplied by