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Surface Chemistry of InP Quantum Dots: A Comprehensive Study

机译:InP量子点的表面化学:全面的研究

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摘要

Advanced ~1H, ~(13)C, and ~(31)P solution and solid-state NMR studies combined with IR spectroscopy were used to probe, at the molecular scale, the composition and the surface chemistry of indium phosphide (InP) quantum dots (QDs) prepared via a non-coordinating solvent strategy. This nanomaterial can be described as a core-multishell object: an InP core, with a zinc blende bulk structure, is surrounded first by a partially oxidized surface shell, which is itself surrounded by an organic coating. This organic passivating layer is composed, in the first coordination sphere, of tightly bound palmitate ligands which display two different bonding modes. A second coordination sphere includes an unexpected dialkyl ketone and residual long-chain non-coordinating solvents (ODE and its isomers) which interact through weak intermolecular bonds with the alkyl chains of the carboxylate ligands. We show that this ketone is formed during the synthesis process via a decarboxylative coupling route and provides oxidative conditions which are responsible for the oxidation of the InP core surface. This phenomenon has a significant impact on the photoluminescence properties of the as-synthesized QDs and probably accounts for the failure of further growth of the InP core.
机译:使用先进的〜1H,〜(13)C和〜(31)P溶液以及固态NMR研究与红外光谱相结合,以分子尺度探测磷化铟(InP)量子的组成和表面化学通过非配位溶剂策略制备的点(QD)。可以将这种纳米材料描述为核-多壳物体:具有锌混合主体结构的InP核首先被部分氧化的表面壳包围,该表面壳本身被有机涂层包围。在第一配位领域中,该有机钝化层由紧密结合的棕榈酸酯配体组成,其显示出两种不同的键合模式。第二个配位球包括意外的二烷基酮和残留的长链非配位溶剂(ODE及其异构体),它们通过弱分子间键与羧酸盐配体的烷基链相互作用。我们表明,该酮是在合成过程中通过脱羧偶联途径形成的,并提供了负责InP核心表面氧化的氧化条件。这种现象对合成后的量子点的光致发光性能产生重大影响,并且可能是造成InP核心进一步增长失败的原因。

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  • 来源
    《Journal of the American Chemical Society》 |2010年第51期|p.18147-18157|共11页
  • 作者单位

    Universite de Toulouse, INSA, UPS, CNRS, LPCNO (Laboratoire de Physique et Chimie des Nano-Objets), 135 avenue de Rangueil, F-31077 Toulouse, France;

    rnUniversite de Toulouse, INSA, UPS, CNRS, LPCNO (Laboratoire de Physique et Chimie des Nano-Objets), 135 avenue de Rangueil, F-31077 Toulouse, France;

    rnUniversite de Toulouse, INSA, UPS, CNRS, LPCNO (Laboratoire de Physique et Chimie des Nano-Objets), 135 avenue de Rangueil, F-31077 Toulouse, France;

    rnUniversite de Toulouse, INSA, UPS, CNRS, LPCNO (Laboratoire de Physique et Chimie des Nano-Objets), 135 avenue de Rangueil, F-31077 Toulouse, France;

    rnLaboratoire de Chimie de Coordination, UPR-CNRS 8241, 205 route de Narbonne, 31077 Toulouse Cedex, France;

    rnUniversite de Toulouse, INSA, UPS, CNRS, LPCNO (Laboratoire de Physique et Chimie des Nano-Objets), 135 avenue de Rangueil, F-31077 Toulouse, France,Laboratoire de Chimie de Coordination, UPR-CNRS 8241, 205 route de Narbonne, 31077 Toulouse Cedex, France;

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