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Functional Si and CdSe quantum dots: Synthesis, conjugate formation, and photoluminescence quenching by surface interactions

机译:功能性Si和CdSe量子点:合成,共轭形成和通过表面相互作用的光致发光猝灭

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摘要

Silicon quantum dots (QDs) were prepared with a corona of di-n-octyl phosphine oxides, by performing hydrosilylation chemistry on the surface of hydrogen-terminated Si QDs. These novel Si QDs proved well-suited to serve as "ligands" for other semiconductor QDs, such as CdSe, by interaction of the phosphine oxide corona with the CdSe surface. A pronounced photoluminescence quenching of CdSe quantum dots was observed upon introduction of the phosphine oxide functionalized Si QDs to a CdSe QD solution. Surface functionalization of the Si QDs proved critically important to observing these effects, as conventional (alkane-covered) Si QD samples gave no evidence of electronic interactions with TOPO-covered CdSe. In a comparative system, phosphine oxide terminated oligo(phenylene vinylene) molecules acting as CdSe QD ligands provide a similar fluorescence quenching, with exciton decay kinetics supporting the formation of an electronically interacting hybrid materials system.
机译:通过在氢封端的Si QDs的表面上进行氢化硅烷化化学反应,用二正辛基膦氧化物的电晕制备硅量子点(QD)。通过氧化膦电晕与CdSe表面的相互作用,证明这些新颖的Si QD非常适合用作其他半导体QD(例如CdSe)的“配体”。在将氧化膦官能化的Si QD引入CdSe QD溶液后,观察到CdSe量子点的显着光致发光猝灭。事实证明,Si QD的表面功能化对于观察这些影响至关重要,因为常规的(烷烃覆盖的)Si QD样品并未提供与TOPO覆盖的CdSe发生电子相互作用的证据。在一个比较系统中,充当CdSe QD配体的氧化膦末端的低聚亚苯基亚乙烯基分子提供了相似的荧光猝灭,并且激子衰减动力学支持电子相互作用的杂化材料系统的形成。

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