首页> 外文期刊>Journal of the American Chemical Society >Negative Polaron and Triplet Exciton Diffusion in Organometaliic 'Molecular Wires'
【24h】

Negative Polaron and Triplet Exciton Diffusion in Organometaliic 'Molecular Wires'

机译:有机金属“分子线”中的负极化子和三重态激子扩散。

获取原文
获取原文并翻译 | 示例
           

摘要

The dynamics of negative polaron and triplet exciton transport within a series of monodisperse platinum (Pt) acetylide oligomers is reported. The oligomers consist of Pt-acetylide repeats, [PtL_2-C=C-Ph-O=C-], (where L = PB113 and Ph = 1,4-phenylene, n = 2, 3, 6, and 10), capped with naphthalene diimide (NDI) end groups. The Pt-acetylide segments are electro- and photoactive, and they serve as conduits for transport of electrons (negative polaron) and triplet excitons. The NDI end groups are relatively strong acceptors, serving as traps for the carriers. Negative polaron transport is studied by using pulse radiolysis/transient absorption at the Brookhaven National Laboratory Laser-Electron Accelerator Facility (LEAF). Electrons are rapidly attached to the oligomers, with some fraction initially residing upon the Pt-acetylide chains. The dynamics of transport are resolved by monitoring the spectral changes associated with transfer of electrons from the chain to the NDI end group. Triplet exciton transport is studied by femtosecond-picosecond transient absorption spectroscopy. Near-UV excitation leads to rapid production of triplet excitons localized on the Pt-acetylide chains. The excitons transport to the chain ends, where they are annihilated by charge separation with the NDI end group. The dynamics of triplet transport are resolved by transient absorption spectroscopy, taking advantage of the changes in spectra associated with decay of the triplet exciton and rise of the charge-separated state. The results indicate that negative polarons and excitons are transported rapidly, on average moving distances of ~3 nm in less than 200 ps. Analysis of the dynamics suggests diffusive transport by a site-to-site hopping mechanism with hopping times of ~27 ps for triplets and <10 ps for electrons.
机译:报道了一系列单分散的铂(Pt)乙炔低聚物中负极化子和三重态激子传输的动力学。该低聚物由Pt-乙炔化物重复序列[PtL_2-C = C-Ph-O = C-](其中L = PB113和Ph = 1,4-亚苯基,n = 2、3、6和10)组成,用萘二酰亚胺(NDI)端基封端。 Pt-乙炔化物链段具有电活性和光活性,它们充当电子(负极化子)和三重态激子传输的通道。 NDI端基是相对较强的受体,充当载体的陷阱。在布鲁克海文国家实验室激光电子加速器设施(LEAF)中使用脉冲辐射分解/瞬态吸收研究了极化子负迁移。电子迅速连接到低聚物上,其中一部分最初位于Pt-乙炔化物链上。通过监测与电子从链到NDI端基转移相关的光谱变化,可以解决传输动力学问题。通过飞秒-皮秒瞬态吸收光谱研究了三重态激子的传输。近紫外线激发导致快速生成位于Pt-乙炔链上的三重态激子。激子运至链端,在此处通过与NDI端基的电荷分离而消灭。利用瞬态吸收光谱法解决了三重态输运的动力学问题,利用了与三重态激子衰变和电荷分离态上升相关的光谱变化。结果表明,负极化子和激子快速迁移,在小于200 ps的平均移动距离约为3 nm。动力学分析表明,通过点对点跳跃机制的扩散传输具有三重态的跳跃时间约为27 ps,而电子的跳跃时间则小于10 ps。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2011年第29期|p.11289-11298|共10页
  • 作者单位

    Department of Chemistry, University of Florida, P.O. Box 117200, Gainesville, Florida 32611, United States;

    Department of Chemistry, Bowling Green State University, Bowling Green, Ohio 43403, United States;

    Department of Chemistry, Bowling Green State University, Bowling Green, Ohio 43403, United States;

    Chemistry Department, Brookhaven National Laboratory, Upton, New York 11973, United States;

    Chemistry Department, Brookhaven National Laboratory, Upton, New York 11973, United States;

    Chemistry Department, Brookhaven National Laboratory, Upton, New York 11973, United States;

    Department of Chemistry, University of Florida, P.O. Box 117200, Gainesville, Florida 32611, United States;

    Chemistry Department, Brookhaven National Laboratory, Upton, New York 11973, United States;

    Department of Chemistry, University of Florida, P.O. Box 117200, Gainesville, Florida 32611, 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
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号