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Size-Programmed Synthesis of PbSe Quantum Dots via Secondary Phosphine Chalcogenides

机译:通过次级膦硫代硫胺化物的尺寸编程的PBSE量子点合成

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In the most common syntheses of colloidal nanocrystal quantum dots (QDs), the size of the particle increases monotonically with reaction time. We have discovered a PbSe QD synthesis whereby size can be easily controlled by varying the side-chains of a secondary phosphine selenide precursor. The reaction runs to completion, and thus a desired QD diameter can be achieved by simply selecting an appropriate secondary phosphine. Quenching of the reaction to select a desired QD size is not required. For different secondary phosphine selenides, measurements of the precursor conversion rate show a direct relationship with final QD size, while P=Se bond strength calculations show an unexpected inverse relationship between QD size and P=Se bond strength. Finally, it is also demonstrated that secondary phosphine selenide precursors can provide an effective route for IV-VI QD syntheses on the large scale.
机译:在最常见的胶体纳米晶体点(QDS)中,颗粒的尺寸随反应时间单调增加。 我们已经发现了一种PBSE QD合成,通过改变次级磷酸硒化酶前体的侧链,可以容易地控制尺寸。 反应完成以完成,因此通过简单地选择合适的仲膦可以实现所需的QD直径。 不需要淬火反应以选择所需的QD尺寸。 对于不同的次级磷酸硒化烷基,前体转化率的测量显示与最终QD尺寸的直接关系,而P = SE键合强度计算显示QD尺寸和P = SE键合强度之间意外的逆关系。 最后,还证明仲膦硒化物前体可以为大规模的IV-VI QD合成提供有效的途径。

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