H-Doped Black Titania with Very High Solar Absorption and Excellent Photocatalysis Enhanced by Localized Surface Plasmon Resonance
Black TiO2 attracts enormous attention due to its large solar absorption and induced excellent photocatalytic activity. Herein, a new approach assisted by hydrogen plasma to synthesize unique H‐doped black titania with a core/shell structure (TiO2@TiO2‐xHx) is presented, superior to the high H2‐pres...
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Veröffentlicht in: | Advanced functional materials 2013-11, Vol.23 (43), p.5444-5450 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Black TiO2 attracts enormous attention due to its large solar absorption and induced excellent photocatalytic activity. Herein, a new approach assisted by hydrogen plasma to synthesize unique H‐doped black titania with a core/shell structure (TiO2@TiO2‐xHx) is presented, superior to the high H2‐pressure process (under 20 bar for five days). The black titania possesses the largest solar absorption (≈83%), far more than any other reported black titania (the record (high‐pressure): ≈30%). H doping is favorable to eliminate the recombination centers of light‐induced electrons and holes. High absorption and low recombination ensure the excellent photocatalytic activity for the black titania in the photo‐oxidation of organic molecules in water and the production of hydrogen. The H‐doped amorphous shell is proposed to play the same role as Ag or Pt loading on TiO2 nanocrystals, which induces the localized surface plasma resonance and black coloration. Photocatalytic water splitting and cleaning using TiO2‐xHx is believed to have a bright future for sustainable energy sources and cleaning environment.
H‐doped black titania with a crystalline core/amorphous shell structure (TiO2@TiO2‐xHx) is synthesized by hydrogen plasma. Solar absorption is enhanced due to localized surface plasmon resonance. H doping reduces oxygen vacancies and eliminates the recombination of light‐excited electrons and holes. These behaviors enable the black titania to be excellent for water splitting. |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.201300486 |