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首页> 外文期刊>ACS catalysis >Driving Surface Redox Reactions in Heterogeneous Photocatalysis: The Active State of Illuminated Semiconductor-Supported Nanoparticles during Overall Water-Splitting
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Driving Surface Redox Reactions in Heterogeneous Photocatalysis: The Active State of Illuminated Semiconductor-Supported Nanoparticles during Overall Water-Splitting

机译:在非均相光催化中驱动表面氧化还原反应:在整个水分裂过程中照明半导体支持的纳米颗粒的活性状态

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摘要

Materials used for photocatalytic overall water splitting (POWS) are typically composed of light-absorbing semiconductor crystals, functionalized with so-called cocatalytic nanoparticles to improve the kinetics of the hydrogen and/or oxygen evolution reactions. While function, quantity, and protection of such metal(oxide) nanoparticles have been addressed in the literature of photocatalysis, the stability and transients in the active oxidation-state upon illumination have received relatively little attention. In this Perspective, the latest insights in the active state of frequently applied cocatalysts systems, including Pt, Rh/Cr2O3, or Ni/NiOx, will be presented. While the initial morphology and oxidation state of such nanoparticles is a strong function of the applied preparation procedure, significant changes in these properties can occur during water splitting. We discuss these changes in relation to the nature of the cocatalyst/semiconductor interface. We also show how know-how of other disciplines such as heterogeneous catalysis or electro-catalysis and recent advances in analytical methodology can help to determine the active state of cocatalytic nanoparticles in photocatalytic applications.
机译:用于光催化整体水分裂(猪)的材料通常由光吸收半导体晶体构成,用所谓的助催化纳米颗粒官能化,以改善氢气和/或氧气进化反应的动力学。虽然在光催化的文献中已经解决了这种金属(氧化物)纳米颗粒的功能,数量和保护,但照明时,活性氧化状态的稳定性和瞬变受到相对较少的关注。在这种观点中,将提出常用助催化剂系统的最新见解,包括Pt,Rh / Cr2O3或Ni / NiOx,包括Pt,Rh / Cr2O3或Ni / NiOx。虽然这种纳米颗粒的初始形态和氧化状态是所施加的制剂过程的强功能,但在水分裂过程中可能发生这些性质的显着变化。我们讨论了与Cocatalyst /半导体界面的性质有关的这些变化。我们还展示了如何授予的其他学科,例如异构催化或电催化和分析方法的最近进步可以有助于确定光催化应用中的助催化纳米粒子的活性状态。

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