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Water Splitting on Composite Plasmonic-Metal/Semiconductor Photoelectrodes: Evidence for Selective Plasmon-lnduced Formation of Charge Carriers near the Semiconductor Surface

机译:复合等离子金属/半导体光电极上的水分解:选择性等离子诱导的在半导体表面附近形成电荷载流子的证据

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摘要

A critical factor limiting the rates of photo-catalytic reactions, including water splitting, on oxide semiconductors is the high rate of charge-carrier recombination. In this contribution, we demonstrate that this issue can be alleviated significantly by combining a semiconductor photocatalyst with tailored plasmonic-metal nanostructures. Plasmonic nanostructures support the formation of resonant surface plasmons in response to a photon flux, localizing electromagnetic energy dose to their surfaces. We present evidence that the interaction of localized electric fields with the neighboring semiconductor allows for the selective formation of electron/hole (e~-/h~+) pairs in the near-surface region of the semiconductor. The advantage of the formation of e~-/h~+ pairs near the semiconductor surface is that these charge carriers are readily separated from each other and easily migrate to the surface, where they can perform photocatalytic transformations.
机译:限制氧化物半导体上光催化反应(包括水分解)的速率的关键因素是电荷-载流子复合的高速率。在这项贡献中,我们证明了通过将半导体光催化剂与定制的等离激元金属纳米结构相结合,可以大大缓解该问题。等离子体纳米结构响应光子通量支持共振表面等离子体激元的形成,将电磁能剂量局限在其表面。我们提供的证据表明,局部电场与相邻半导体的相互作用允许在半导体的近表面区域中选择性形成电子/空穴(e〜-/ h〜+)对。在半导体表面附近形成e _- / h〜+对的优点是,这些电荷载流子易于彼此分离并易于迁移到表面,在此处它们可以进行光催化转化。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2011年第14期|p.5202-5205|共4页
  • 作者

    David B.Ingram; Suljo Linic;

  • 作者单位

    Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, United States;

    Department of Chemical Engineering, University of Michigan, Ann Arbor, Michigan 48109, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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