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Hao Yin

Researcher at China Academy of Engineering Physics

Publications -  27
Citations -  2945

Hao Yin is an academic researcher from China Academy of Engineering Physics. The author has contributed to research in topics: Photocatalysis & Titanium dioxide. The author has an hindex of 14, co-authored 25 publications receiving 2516 citations. Previous affiliations of Hao Yin include Beijing Institute of Technology & Shanghai Jiao Tong University.

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H‐Doped Black Titania with Very High Solar Absorption and Excellent Photocatalysis Enhanced by Localized Surface Plasmon Resonance

TL;DR: In this article, a new approach assisted by hydrogen plasma to synthesize unique H-doped black titania with a core/shell structure was presented, superior to the high H-2-pressure process (under 20 bar for five days).
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Visible-light photocatalytic, solar thermal and photoelectrochemical properties of aluminium-reduced black titania

TL;DR: In this article, a mass production approach to synthesize black titania by aluminium reduction is reported, and the obtained sample possesses a unique crystalline core-amorphous shell structure (TiO2@TiO 2−x).
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Core-shell nanostructured "black" rutile titania as excellent catalyst for hydrogen production enhanced by sulfur doping.

TL;DR: An innovative two-step method to prepare a core-shell nanostructured S-doped rutile TiO2 (R'-TiO2-S) sample exhibits remarkably enhanced absorption in visible and near-infrared regions and efficient charge separation and transport.
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Effective nonmetal incorporation in black titania with enhanced solar energy utilization

TL;DR: In this paper, nonmetal-doped black titania is achieved in a core-shell structure by a two-step synthesis, and the nonmetal dopants in amorphous TiO2−x shells decrease e-h recombination centers, and more than 6.6 at.% N further improves solar energy absorption from 65% up to 85%.
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Black TiO2 nanotube arrays for high-efficiency photoelectrochemical water-splitting

TL;DR: In this paper, the black titania nanotubes with substantial Ti3+ and oxygen vacancies exhibit an excellent photoelectrochemical water-splitting performance due to the improved charge transport and separation and the extended visible light response.