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Thang Duy Dao

Researcher at National Institute for Materials Science

Publications -  103
Citations -  3382

Thang Duy Dao is an academic researcher from National Institute for Materials Science. The author has contributed to research in topics: Plasmon & Thin film. The author has an hindex of 28, co-authored 96 publications receiving 2419 citations. Previous affiliations of Thang Duy Dao include Nara Institute of Science and Technology & Hokkaido University.

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Surface-Plasmon-Enhanced Photodriven CO2 Reduction Catalyzed by Metal-Organic-Framework-Derived Iron Nanoparticles Encapsulated by Ultrathin Carbon Layers.

TL;DR: By carbon layer coating, the optimized catalyst exhibits enhanced selectivity and stability applied to the solar-driven reduction of CO2 into CO through the surface-plasmon effect of iron particles, and thereby facilitates the final reaction activity.
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Conversion of Carbon Dioxide by Methane Reforming under Visible-Light Irradiation: Surface-Plasmon-Mediated Nonpolar Molecule Activation

TL;DR: In this paper, a novel CO2 photoreduction method, CO2 conversion through methane reforming into syngas (DRM), was adopted as an efficient approach to not only reduce the environmental concentration of the greenhouse gas CO2 but also realize the net energy storage from solar energy to chemical energy.
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Infrared Perfect Absorbers Fabricated by Colloidal Mask Etching of Al–Al2O3–Al Trilayers

TL;DR: In this article, a combined fabrication method of reactive ion etching and large-scale colloidal mask was proposed to fabricate mid-infrared metamaterial perfect absorbers using aluminum.
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Light-Enhanced Carbon Dioxide Activation and Conversion by Effective Plasmonic Coupling Effect of Pt and Au Nanoparticles

TL;DR: It is reported that the plasmonic coupling effect of Pt and Au nanoparticles (NPs) profoundly enhances the efficiency of CO2 reduction through dry reforming of methane reaction assisted by light illumination, reducing activation energies forCO2 reduction ∼30% below thermal activation energies and achieving a reaction rate 2.4 times higher than that of the thermocatalytic reaction.