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Alternating layer addition approach to CdSe/CdS core/shell quantum dots with near-unity quantum yield and high on-time fractions

机译:具有接近统一的量子产率和高导通时间分数的CdSe / CdS核/壳量子点的交替层添加方法

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We report single-particle photoluminescence (PL) intermittency (blinking) with high on-time fractions in colloidal CdSe quantum dots (QD) with conformal CdS shells of 1.4 nm thickness, equivalent to approximately 4 CdS monolayers. All QDs observed displayed on-time fractions >60% with the majority >80%. The high on-time fraction blinking is accompanied by fluorescence quantum yields (QY) close to unity (up to 98% in an absolute QY measurement) when dispersed in organic solvents and a monoexponential ensemble photoluminescence (PL) decay lifetime. The CdS shell is formed in high synthetic yield using a modified selective ion layer adsorption and reaction (SILAR) technique that employs a silylated sulfur precursor. The CdS shell provides sufficient chemical and electronic passivation of the QD excited state to permit water solubilization with greater than 60% QY via ligand exchange with an imidazole-bearing hydrophilic polymer.
机译:我们报告胶体CdSe量子点(QD)具有1.4 nm厚度的保形CdS壳,相当于大约4个CdS单层的高导通时间分数的单粒子光致发光(PL)间歇性(闪烁)。观察到的所有QD均显示出按时分数> 60%,大多数> 80%。当分散在有机溶剂中时,高导通时间的分数闪烁伴随着接近统一的荧光量子产率(QY)(在绝对QY测量中高达98%)和单指数集成光致发光(PL)衰减寿命。使用改良的选择性离子层吸附和反应(SILAR)技术(采用甲硅烷基化的硫前体)以高合成产率形成CdS壳。 CdS壳提供了QD激发态的足够的化学和电子钝化,以允许通过与含咪唑的亲水性聚合物进行配体交换而使QY大于60%的水溶解。

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