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Kazuhiko Mase

Researcher at Graduate University for Advanced Studies

Publications -  199
Citations -  2979

Kazuhiko Mase is an academic researcher from Graduate University for Advanced Studies. The author has contributed to research in topics: X-ray photoelectron spectroscopy & Ion. The author has an hindex of 27, co-authored 199 publications receiving 2584 citations. Previous affiliations of Kazuhiko Mase include Chiba University & University of Tokyo.

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In situ ambient pressure XPS study of CO oxidation reaction on Pd(111) surfaces

TL;DR: In this article, the CO oxidation reaction on the Pd(111) model catalyst at various temperatures (200 −400 °C) under hundreds mTorr pressure conditions has been monitored by in situ ambient pressure X-ray photoelectron spectroscopy.
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Control of the interchain π-π interaction and electron density distribution at the surface of conjugated poly(3-hexylthiophene) thin films

TL;DR: It can be deduced that the slower removal rate of the solvent makes the polymer chains even at the surface have sufficient time to adopt a more nearly equilibrium structure with edge-on conformation, which buries the pi-electron density contributed from the polymer backbone.
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Adsorbate-driven reactive interfacial Pt-NiO1−x nanostructure formation on the Pt3Ni(111) alloy surface

TL;DR: It is shown that the inherent lattice mismatch of bimetallic materials selectively creates surface segregation of subsurface metal atoms, which is responsible for a highly efficient step in the CO oxidation reaction.
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Epitaxial Rh-doped SrTiO3 thin film photocathode for water splitting under visible light irradiation

TL;DR: In this article, the valence of the Rh dopant in the rh:SrTiO3 films was found to have a p-type behavior under visible light irradiation, reproducing the known optical absorption behavior of powder samples.
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Active Surface Oxygen for Catalytic CO Oxidation on Pd(100) Proceeding under Near Ambient Pressure Conditions.

TL;DR: In-situ observation of the reaction reveals that two reaction pathways switch over alternatively depending on the surface temperature, which is likely that the enhanced rate of CO2 formation is associated with an active oxygen species that is located at the surface of the trilayer oxide.