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Photocatalytic hydrogen or oxygen evolution from water over S, or N-doped TiO2 under visible light

机译:在可见光下,水在S或N掺杂的TiO2上从水中释放出的光催化氢或氧

摘要

S- or N-doping of TiO2 powder having an anatase or rutile phase extended the photocatalytic activity for water oxidation and reduction under UV light and visible light irradiation. For the reduction of water, anatase-doped TiO2 showed higher level of activity than that of doped TiO2 having a rutile phase using ethanol as an electron donor. Furthermore, the activity level of S-doped TiO2 for hydrogen evolution was higher than that of N-doped TiO2 photocatalysts under visible light. Photocatalytic oxidation of water on doped TiO2 having a rutile phase proceeded with fairly high efficiency when Fe3⁺ ions were used as electron acceptors compared to that on doped TiO2 having an anatase phase. In addition, water splitting under visible light irradiation was achieved by construction of a Z-scheme photocatalysis system employing the doped TiO2 having anatase and rutile phases for H2 and O2 evolution and the I⁻/IO⁻3 redox couple as an electron relay.
机译:具有锐钛矿相或金红石相的TiO2粉末的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。为了减少水,与使用乙醇作为电子给体的具有金红石相的掺杂的TiO2相比,掺杂有锐钛矿的TiO2显示出更高的活性。此外,在可见光下,S掺杂的TiO2析氢活性高于N掺杂的TiO2光催化剂。当使用Fe 3+离子作为电子受体时,与具有锐钛矿相的掺杂TiO 2相比,在具有金红石相的掺杂的TiO 2上水的光催化氧化以相当高的效率进行。另外,在可见光照射下的水分解是通过构造Z-方案光催化系统实现的,该系统使用具有锐钛矿和金红石相的掺杂的TiO 2来释放H 2和O 2,并将I 3 / IO 3氧化还原对作为电子中继。

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