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Charge Transfer to LaAlO3/SrTiO3 Interfaces Controlled by Surface Water Adsorption and Proton Hopping

机译:电荷转移至受表面水吸附和质子跳跃控制的LaAlO3 / SrTiO3界面

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摘要

Electronic properties of low dimensional systems are particularly sensitive to surface adsorbates. Clear understanding of such phenomena can lead to highly effective and nondestructive material engineering techniques. In this work, water adsorption at the surface of LaAlO3/SrTiO3 heterostructures is systematically studied. The saturation of surface dangling bonds by spontaneous water chemisorptions is found to be a main enabler of the formation of the interface 2D electron gas. In particular, when imbalanced distributions of water based ions, namely protons and hydroxyls, are generated, interface electron doping or depletion becomes surface adsorbates dominant and independent of the LaAlO3 layer thickness. The investigations also reveal the importance of hydrogen bonding through molecular water layers, which provides an energetically feasible pathway for manipulating the surface-bond protons and thus the interface electrical characteristics.
机译:低维系统的电子性质对表面吸附物特别敏感。对此类现象的清晰理解可以导致高效且无损的材料工程技术。在这项工作中,系统地研究了LaAlO3 / SrTiO3异质结构表面的水吸附。发现自发水化学吸附引起的表面悬空键的饱和是界面2D电子气形成的主要推动力。特别地,当产生水基离子即质子和羟基的不平衡分布时,界面电子的掺杂或耗尽成为表面吸附物占主导地位,并且与LaAlO3层厚度无关。研究还揭示了通过分子水层进行氢键键合的重要性,这为操纵表面键合质子以及界面电学特性提供了一条在能量上可行的途径。

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  • 来源
    《Advanced Functional Materials》 |2016年第30期|5453-5459|共7页
  • 作者单位

    West Virginia Univ, Dept Phys & Astron, Morgantown, WV 26506 USA;

    Univ Liege, Phys Theor Mat, B-4000 Sart Tilman Par Liege, Belgium|IPN, Ctr Invest & Estudios Avanzados, MX-76230 Queretaro, Mexico;

    West Virginia Univ, Dept Phys & Astron, Morgantown, WV 26506 USA;

    Univ Wisconsin, Dept Mat Sci & Engn, Madison, WI 53706 USA;

    Univ Wisconsin, Dept Mat Sci & Engn, Madison, WI 53706 USA;

    Univ Wisconsin, Dept Mat Sci & Engn, Madison, WI 53706 USA;

    Univ Wisconsin, Dept Mat Sci & Engn, Madison, WI 53706 USA;

    West Virginia Univ, Dept Phys & Astron, Morgantown, WV 26506 USA;

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