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首页> 外文期刊>International Journal of Photoenergy >Photocatalytic Hydrogen or Oxygen Evolution from Water over S- or N-DopedTiO2under Visible Light
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Photocatalytic Hydrogen or Oxygen Evolution from Water over S- or N-DopedTiO2under Visible Light

机译:可见光下S或N掺杂TiO2上水的光催化氢或氧释放

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摘要

S- or N-doping ofTiO2powder having an anatase or rutile phase extended thephotocatalytic activity for water oxidation and reduction under UV light and visible lightirradiation. For the reduction of water, anatase-dopedTiO2showed higher level ofactivity than that of dopedTiO2having a rutile phase using ethanol as an electron donor.Furthermore, the activity level of S-dopedTiO2for hydrogen evolution was higher thanthat of N-dopedTiO2photocatalysts under visible light. Photocatalytic oxidation of wateron dopedTiO2having a rutile phase proceeded with fairly high efficiency whenFe3+ionswere used as electron acceptors compared to that on dopedTiO2having an anatase phase.In addition, water splitting under visible light irradiation was achieved by construction ofa Z-scheme photocatalysis system employing the dopedTiO2having anatase and rutilephases forH2andO2evolution and theI−/IO3−redox couple as an electron relay.
机译:具有锐钛矿相或金红石相的TiO2粉体的S或N掺杂扩展了在水和紫外光和可见光照射下水氧化和还原的光催化活性。在水的还原方面,锐钛矿型掺杂的TiO2的活性水平高于以乙醇为电子供体的金红石型掺杂的金红石型掺杂的TiO2。当Fe3 +离子用作电子受体时,与具有锐钛矿相的掺杂TiO2相比,水对金红石型掺杂TiO2的光催化效率更高。掺杂的TiO2具有锐钛矿和金红石相,用于H2和O2的演化,I- / IO3-氧化还原对作为电子中继。

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