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Ab Initio Nonadiabatic Molecular Dynamics of the Ultrafast Electron Injection from a PbSe Quantum Dot into the TiO_2 Surface

机译:从PbSe量子点到TiO_2表面的超快电子注入的从头算非绝热分子动力学

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摘要

Following recent experiments [Science 2010, 328, 1543; PNAS 2011, 108, 965], we report an ab initio nonadiabatic molecular dynamics (NAMD) simulation of the ultrafast photoinduced electron transfer (ET) from a PbSe quantum dot (QD) into the rutile TiO_2 (110) surface. The system forms the basis for QD-sensitized semiconductor solar cells and demonstrates that ultrafast interfacial ET is instrumental for achieving high efficiencies in solar-to-electrical energy conversion. The simulation supports the observation that the ET successfully competes with energy losses due to electron-phonon relaxation. The ET proceeds by the adiabatic mechanism because of strong donor-acceptor coupling. High frequency polar vibrations of both QD and TiO_2 promote the ET, since these modes can rapidly influence the donor-acceptor state energies and coupling. Low frequency vibrations generate a distribution of initial conditions for ET, which shows a broad variety of scenarios at the single-molecule level. Compared to the molecule-TiO_2 interfaces, the QD-TiO_2 system exhibits pronounced differences that arise due to the larger size and higher rigidity of QDs relative to molecules. Both donor and acceptor states are more delocalized in the QD system, and the ET is promoted by optical phonons, which have relatively low frequencies in the QD materials composed of heavy elements. In contrast, in molecular systems, optical phonons are not thermally accessible under ambient conditions. Meanwhile, TiO_2 acceptor states resemble surface impurities due to the local influence of molecular chromophores. At the same time, the photoinduced ET at both QD-TiO_2 and molecule-TiO_2 interfaces is ultrafast and occurs by the adiabatic mechanism, as a result of strong donor-acceptor coupling. The reported state-of-the-art simulation generates a detailed time-domain atomistic description of the interfacial ET process that is fundamental to a wide variety of applications.
机译:根据最近的实验[Science 2010,328,1543; [PNAS 2011,108,965],我们报告了从PbSe量子点(QD)到金红石TiO_2(110)表面的超快光诱导电子转移(ET)的从头算起非绝热分子动力学(NAMD)模拟。该系统构成了QD敏感型半导体太阳能电池的基础,并证明了超快界面ET对于实现太阳能到电能的高效转换是有帮助的。该仿真支持以下观察:ET成功地克服了由于电子声子弛豫引起的能量损失。由于强的供体-受体偶联,ET通过绝热机理进行。 QD和TiO_2的高频极性振动都会促进ET,因为这些模式会迅速影响施主-受主的态能和耦合。低频振动会产生ET初始条件的分布,这表明在单分子水平上存在多种情况。与分子-TiO_2界面相比,QD-TiO_2系统表现出明显的差异,这是由于相对于分子而言,QD的尺寸更大且刚性更高。供体和受体态在QD系统中都更加局域化,并且ET由光学声子促进,该声子在由重元素组成的QD材料中具有相对较低的频率。相反,在分子系统中,光子在环境条件下是不易热接触的。同时,由于分子发色团的局部影响,TiO_2受体状态类似于表面杂质。同时,由于强的供体-受体耦合,QD-TiO_2和分子-TiO_2界面处的光诱导ET都非常快,并且是通过绝热机理发生的。所报告的最新模拟会生成界面ET过程的详细时域原子描述,这是各种应用程序的基础。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2011年第47期|p.19240-19249|共10页
  • 作者

    Run Long; Oleg V. Prezhdo;

  • 作者单位

    Department of Chemistry, University of Rochester, New York 14627, United States,School of Chemical & Bioprocess Engineering, University College Dublin, Ireland;

    Department of Chemistry, University of Rochester, New York 14627, 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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