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Observation of biexcitons in the presence of trions generated via sequential absorption of multiple photons in colloidal quantum dot solids

机译:在胶体量子点固体中依次吸收多个光子而产生的tri子存在下的双激子的观察

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Multi exciton generation (MEG) and multi exciton recombination (MER) in semiconductor quantum dots (QDs) have recently attracted significant scientific interest as a possible means to improve device efficiencies [1–5]. Convenient bandgap tunability, easy colloidal synthesis, and solution-based processability of these QDs make them further attractive for such device applications using MEG and MER. For example, recent theoretical and experimental studies have shown that MEG enables >100% peak external quantum efficiency where the generated multi excitons (MEs) are collected in a simple QD solar cell structure [1]. Furthermore, MEG has also been shown in QD photodetectors exhibiting substantially increased photocurrent levels [2]. Another promising application for MEs is the use of QDs as an alternative gain medium based on MER for lasers. Although MEG is very promising and supported with quite persuasive reports, there are still some debatable issues that need to be clarified. One of the issues that have generated great debates in the field has been the confusion of MER with the recombination of trions, which takes place in photocharged QDs. To utilize MEG and MER in practical devices such as QD solar cells and QD lasing devices, these phenomena need to be well understood. Here, we showed distinct spectrally-resolved temporal behavior of biexciton (BX), single exciton (X) and trion radiative recombinations in near unity quantum yield (QY) quasi-type II CdSe/CdS core/shell nanocrystal QDs. Upon sequential absorption of multiple photons, the extraction of Xs, BXs, and trions were achieved using time correlated single photon counting (TCSPC) measurements performed on low concentration thin film samples of these QDs at different emission wavelengths. The QDs were embedded in PMMA medium to obtain homogeneous samples and avoid Förster-type nonradiative energy transfer (NRET) between them. Here to extract Xs, BXs, and trions, we devised a new analys- s approach for the time decays of the QDs that allowed us to attribute the physical events to their corresponding time decay terms, which were further verified with their excitation intensity dependencies [6].
机译:半导体量子点(QD)中的多激子产生(MEG)和多激子复合(MER)最近引起了广泛的科学兴趣,作为提高器件效率的一种可能方法[1-5]。这些QD的便捷带隙可调性,容易的胶体合成以及基于溶液的可加工性,使其对于使用MEG和MER的此类设备应用更具吸引力。例如,最近的理论和实验研究表明,MEG可实现> 100%的峰值外部量子效率,其中将生成的多激子(ME)收集在简单的QD太阳能电池结构中[1]。此外,在QD光电探测器中还显示出MEG表现出显着提高的光电流水平[2]。 ME的另一个有希望的应用是将QD用作基于MER的替代增益介质用于激光器。尽管MEG非常有前途并且得到了有说服力的报告的支持,但是仍然有一些值得争论的问题需要澄清。在该领域引起广泛争议的问题之一是MER与光子QD中发生的重子重组有关的混乱。为了在诸如QD太阳能电池和QD激光设备的实际设备中利用MEG和MER,需要很好地理解这些现象。在这里,我们显示了双激子(BX),单激子(X)和三重子辐射重组的明显的光谱分辨时间行为,其准量子产率(QY)准II型CdSe / CdS核/壳纳米晶体QDs。在连续吸收多个光子后,使用时间相关的单光子计数(TCSPC)测量在不同发射波长下对这些QD的低浓度薄膜样品进行测量,即可完成Xs,BXs和tri的提取。将量子点嵌入到PMMA介质中以获得均匀的样本,并避免它们之间的Förster型非辐射能量转移(NRET)。在这里,为了提取Xs,BXs和Trions,我们设计了一种新的QDs时间衰减分析方法,使我们能够将物理事件归因于其相应的时间衰减项,并进一步用其激发强度依赖性进行了验证[ 6]。

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