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Emission properties of colloidal quantum dots on polyelectrolyte multilayers

机译:聚电解质多层膜上胶体量子点的发射特性

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We present steady state and time-resolved photoluminescence (PL) characteristics of differently charged CdTe quantum dots (QDs) adsorbed onto a polyelectrolyte (PE) multilayer. The PE multilayer is built up using a layer-by-layer assembly technique. We find that the diffusion of the QDs into the PE multilayer is an important factor in the case of 3-mercapto-l, 2-propanediol stabilized QDs (neutral surface charge), resulting in a approx 31-fold enhancement in PL intensity accompanied by a blue shift in the PL spectra and an increase in decay lifetime from 3.74 ns to a maximum of 11.65 ns. These modified emission properties are attributed to the enhanced surface related emission resulting from the interaction of the QD's surface with the PE. We find that diffusion does not occur for thioglycolic acid (TGA) stabilized QDs (negative surface charge) or 2-mercaptoethylamine stabilized QDs (positive surface charge), indicating localization of the QDs on top of the PE multilayer. However, the PL lifetime of the TGA stabilized QDs decreases from 9.58 to 5.78 ns with increasing PE multilayer thickness. This provides evidence for increased intrinsic exciton recombination relative to surface related emission, which results in an overall reduction in the average lifetime. Our studies indicate the importance of the QD surface charge in determining the interaction with the PE multilayers and the subsequent modification of the QD emission properties.
机译:我们目前的稳态和时间分辨的光致发光(PL)特性的不同电荷的CdTe量子点(QDs)吸附到聚电解质(PE)多层。 PE多层是使用逐层组装技术构建的。我们发现,在3-巯基-1,2-丙二醇稳定的QD(中性表面电荷)的情况下,QD扩散到PE多层中是一个重要因素,导致PL强度提高了约31倍,并伴随着PL光谱发生蓝移,衰减寿命从3.74 ns增加到最大11.65 ns。这些改进的发射特性归因于由于QD表面与PE相互作用而导致的与表面相关的增强发射。我们发现,对于巯基乙酸(TGA)稳定的QD(负表面电荷)或2-巯基乙胺稳定的QD(正表面电荷)不会发生扩散,这表明QD定位在PE多层膜的顶部。但是,随着PE多层厚度的增加,TGA稳定的QD的PL寿命从9.58 ns降低到5.78 ns。这提供了相对于表面相关发射增加的固有激子复合的证据,这导致平均寿命的整体降低。我们的研究表明,QD表面电荷在确定与PE多层膜的相互作用以及随后改变QD发射特性方面的重要性。

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