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Spontaneous doping of two-dimensional NaCl films with Cr atoms: aggregation and electronic structure

机译:自发的掺杂二维氯化钠的电影与铬原子:聚合和电子结构

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摘要

Scanning tunneling microscopy (STM) experiments combined with density functional theory (DFT) calculations reveal that deposited Cr atoms replace either Na or Cl ions, forming substituting dopants in ultrathin NaCl/Au(111) films. The Cr dopants exchange electrons with the support thus changing the electronic properties of the film and in particular the work function. The Cr atoms spontaneously aggregate near the edges of the bilayer (2L) NaCl islands, forming a new phase in the insulator with a remarkably dense population of Cr dopants. The spectra of differential conductance yield evidence that, compared to the undoped or Cr-poor 2L NaCl films on Au(111), the Cr-rich region shows different interface states, shifted image-potential states, and a reduced work function. This demonstrates the potential of doping ultrathin films to modify their adsorption properties in a desired manner.
机译:扫描隧道显微镜(STM)实验结合密度泛函理论(DFT)计算表明,沉积铬原子取代钠或氯离子,形成取代掺杂物在超薄生理盐水/非盟(111)电影。因此改变电子特性的支持的电影,特别是工作功能。铬原子自发聚合附近双分子层的边缘(2 l)氯化钠岛屿,形成一个在绝缘子非常新阶段Cr掺杂物的稠密的人口。微分电导产生的证据表明,,相比无掺杂或Cr-poor 2 l氯化钠的电影在非盟(111),Cr-rich地区显示不同界面状态,改变幅图景,和减少工作的功能。掺杂超薄电影修改的潜力吸附性能以期望的方式。

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