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Dual-Time Scale Photoinduced Electron Transfer from PbS Quantum Dots to a Molecular Acceptor

机译:从PbS量子点到分子受体的双倍尺度光致电子转移。

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摘要

A combination of picosecond and microsecond transient absorption dynamics reveals the involvement of two mechanisms by which 1,4-benzoquinone (BQ) induces the decay of the excited state of PbS quantum dots (QDs): (i) electron transfer to BQ molecules adsorbed to the surfaces of PbS QDs and (ii) collisionally gated electron transfer to freely diffusing BQ. Together, these two mechanisms quantitatively describe the quenching of photoluminescence upon addition of BQ to PbS QDs in dichloromethane solution. This work represents the first quantitative study of a QD-ligand system that undergoes both adsorbed and collisionally gated photoinduced charge transfer within the same sample. The availability of a collisionally gated pathway improves the yield of electron transfer from PbS QDs to BQ by an average factor of 2.5 over that for static electron transfer alone.
机译:皮秒和微秒瞬态吸收动力学的结合揭示了两种机制的参与,其中1,4-苯醌(BQ)引起PbS量子点(QDs)激发态的衰减:(i)电子转移到吸附到BQ分子上PbS量子点的表面和(ii)碰撞门控电子转移到自由扩散的BQ。一起,这两种机制定量描述了在二氯甲烷溶液中将BQ添加到PbS QD中时猝灭的光致发光。这项工作代表了对QD-配体系统进行的首次定量研究,该系统在同一样品中经历了吸附和碰撞门控的光诱导电荷转移。碰撞门控路径的可用性将电子从PbS量子点到BQ的转移效率提高了2.5倍,高于仅静态电子转移的平均因子。

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  • 来源
    《Journal of the American Chemical Society》 |2012年第30期|p.12470-12473|共4页
  • 作者单位

    Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, United States;

    Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, United States;

    Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113, 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);
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  • 正文语种 eng
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