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Lanthanide-Doped CaS and SrS Luminescent Nanocrystals: A Single-Source Precursor Approach for Doping

机译:镧系元素掺杂的CaS和SrS发光纳米晶体:掺杂的单源前体方法。

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摘要

The incorporation of dopants with optical or magnetic functionalities into colloidal nanocrystals (NCs) has been a longstanding challenge for nanomaterial research. A deeper understanding of the doping kinetics will aid a better control of the doping process. In particular, alkaline-earth sulfides are an important class of host materials for a range of luminescent dopants, including transition-metal and lanthanide ions. Their nanocrystalline analogues have many potential applications. However, the lack of synthetic methodologies hampers their development. Here we introduce a single-source precursor approach that successfully leads to Ce~(3+)- and Eu~(2+)-doped CaS and SrS luminescent NCs with diameters of ~10 nm and with luminescent properties similar to those of the bulk analogues. The characteristic absorption and luminescence of Ce~(3+) and Eu~(2+) depend on the local coordination and are applied to probe dopant ion internalization. We demonstrate that controlling the reactivity of the precursors is crucial for achieving effective doping. By designing the chemical structure of the dopant precursor to vary the reactivity relative to that of the host precursor, the doping efficiency can be controlled. In addition, we have applied a growth doping strategy to further improve internalization of the dopants. Finally, we demonstrate nucleation doping as an alternative method to achieve lanthanide NC doping for dopant and host precursors with strongly different reactivities. The single-source precursor approaches proposed here allow for a flexible design of synthesis strategies and have the potential to be widely applicable to the doping of colloidal chalcogenide NCs with transition-metal and lanthanide dopant ions.
机译:将具有光学或磁性功能的掺杂剂掺入胶体纳米晶体(NC)中一直是纳米材料研究的长期挑战。更深入地了解掺杂动力学将有助于更好地控制掺杂过程。尤其是,碱土金属硫化物是用于一系列发光掺杂剂(包括过渡金属离子和镧系元素离子)的重要主体材料。它们的纳米晶体类似物具有许多潜在的应用。但是,缺乏综合方法论阻碍了它们的发展。在这里,我们介绍了一种单源前驱方法,该方法成功地导致了Ce〜(3+)和Eu〜(2+)掺杂的CaS和SrS发光NC,其直径约为〜10 nm,并且其发光特性与大体积发光相似。类似物。 Ce〜(3+)和Eu〜(2+)的特征吸收和发光取决于局部配位,并应用于探针掺杂离子的内在化。我们证明控制前体的反应性对于实现有效掺杂至关重要。通过设计掺杂剂前体的化学结构以改变相对于主体前体的反应性,可以控制掺杂效率。另外,我们已经应用了生长掺杂策略来进一步改善掺杂剂的内部化。最后,我们展示了成核掺杂作为实现镧系元素NC掺杂的另一种方法,用于掺杂剂和主体前体的反应性非常不同。此处提出的单源前体方法允许灵活设计合成策略,并有可能广泛应用于用过渡金属和镧系元素掺杂离子掺杂胶体硫属元素化物NC。

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  • 来源
    《Journal of the American Chemical Society》 |2014年第47期|16533-16543|共11页
  • 作者单位

    Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, Princetonplein 5, 3584 CC Utrecht, The Netherlands, Translational and Molecular Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA;

    Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, Princetonplein 5, 3584 CC Utrecht, The Netherlands;

    Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, Princetonplein 5, 3584 CC Utrecht, The Netherlands;

    Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, Princetonplein 5, 3584 CC Utrecht, The Netherlands, School of Chemical and Physical Sciences, Flinders University, GPO Box 2100, Adelaide 5001, Australia;

    Department of Chemistry, University of Washington, Seattle, Washington 98195-1700, United States;

    Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, Princetonplein 5, 3584 CC Utrecht, The Netherlands;

    Condensed Matter and Interfaces, Debye Institute for Nanomaterials Science, Utrecht University, Princetonplein 5, 3584 CC Utrecht, The Netherlands;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:11:22

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