7 results match your criteria: "Graduate School of Science and Technology Kumamoto University[Affiliation]"

A perfectly oriented, free-standing and transparent titania nanosheet film was prepared using the spin-coating technique. The free-standing film (thickness: ∼210 nm) showed a wide band gap that corresponded to that of the monolayer nanosheet despite the stacking of hundreds of layers.

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Recently, non-crystalline coordination materials have been shown to represent a versatile class of functional materials. However, such materials incorporating metal complex clusters have remained largely unexplored. Herein, we demonstrate that a luminescent tetranuclear ReV cluster melts at 489 K, with the cluster structure being maintained in the corresponding supercooled ionic liquid phase.

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Vinylidene -quinone methides (s) are one-carbon elongated homologues of -quinone methides (s), well-known as useful reaction intermediates in organic transformations. These related quinone methides are quite distinct in terms of stereochemistry. Namely, s are characterized by an exocyclic allenyl ketone unit merged with a dearomatized ring system and thus, can be rendered axially chiral by locating a substituent properly at the terminal methylene group of the allene moiety.

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Graphene oxide (GO) shows high proton conductivity (≈10 Scm), excellent mechanical stability, and electrical insulation property, which makes it an ideal candidate for use as a proton conducting solid state electrolyte. The prospects of using GO as single phase solid electrolyte in an all solid battery is presented herein. A battery with the cell configuration: Zn + ZnSO•7HO + graphite (anode) || GO (electrolyte) || MnO + graphite (cathode) is fabricated.

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The rapid development of flexible and wearable electronics has led to an increase in the demand for flexible supercapacitors with enhanced electrochemical performance. Graphene oxide (GO) and reduced GO (rGO) exhibit several key properties required for supercapacitor components. Although solid-state rGO/GO/rGO supercapacitors with unique structures are promising, their moderate capacitance is inadequate for practical applications.

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Rh Nanoparticle Anchoring on Metal Phosphates: Fundamental Aspects and Practical Impacts on Catalysis.

Chem Rec

October 2016

Department of Applied Chemistry and Biochemistry, Graduate School of Science and Technology Kumamoto University, 2-39-1 Kurokami, Chuo, Kumamoto, 860-8555, Japan.

Metal phosphates stabilize Rh nanoparticles on their surface via Rh-O-P bonds, in contrast to the Rh-O-M bonds formed on metal oxides (MO ). The local structure, electronic structure, and redox properties of Rh nanoparticles anchored on metal phosphates, and their practical impacts on catalysis, are reviewed based on recent publications from the author's research group. Because of the covalency of the Rh-O-P bond, Rh oxide is readily reduced to metallic Rh having a higher catalytic activity, whereas Rh oxide on metal oxide supports is more difficult to reduce with an increase of the anchoring strength.

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