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Synthesis and Surface Chemistry of Cadmium Carboxylate Passivated CdTe Nanocrystals from Cadmium bis(Phenyltellurolate)

机译:双(苯基碲酸镉)镉的钝化羧酸镉钝化CdTe纳米晶体的合成与表面化学

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We report the synthesis of cadmium telluride nanocrystals from cadmium bis(phenyltellurolate) (Cd(TePh)(2)) and cadmium alkylcarboxylates (Cd(O2CR)(2), O2CR = oleate, tetradecanoate). Cd(TePh)(2) reacts quantitatively with Cd(O2CR)(2) at 220 degrees C over 1 h with the concomitant elimination of diphenyl telluride (Ph2Te) and CdTe nanocrystals. The nanocrystal diameter approaches 3.0-3.2 nm at full conversion regardless of changes to the solvent, carboxylate chain length, heating conditions, and reaction concentration. Larger nanocrystals may be grown by slow addition of additional precursors to the crude product mixture. Isolated nanocrystals have carboxylate ligands (2.1-4.7 nm(-2)) that can be displaced along with excess cadmium ions using low concentrations of N,N,N',N'-tetramethylethylenediamine (TMEDA) (1.5-280 mM). Using H-1 NMR spectroscopy, we measure the extent of the displacement and show that the binding of Cd(O2CR)(2) to CdTe is weaker than to CdSe nanocrystals of similar size. The weaker binding is proposed to arise from a lower polarity and greater stability of reconstructed CdTe surfaces.
机译:我们报告了双(苯基碲脲酸镉)(Cd(TePh)(2))和烷基羧酸镉(Cd(O2CR)(2),O2CR =油酸盐,十四烷酸盐)的碲化镉纳米晶体的合成。 Cd(TePh)(2)在220摄氏度下与Cd(O2CR)(2)在1小时内发生定量反应,同时消除了二苯基碲化物(Ph2Te)和CdTe纳米晶体。无论溶剂,羧酸盐链长,加热条件和反应浓度如何变化,纳米晶在完全转化时的直径均接近3.0-3.2 nm。可以通过将其他前体缓慢添加到粗产物混合物中来生长更大的纳米晶体。分离的纳米晶体具有羧酸盐配体(2.1-4.7 nm(-2)),可以使用低浓度的N,N,N',N'-四甲基乙二胺(TMEDA)(1.5-280 mM)与过量的镉离子一起置换。使用H-1 NMR光谱,我们测量了位移的程度,并表明Cd(O2CR)(2)与CdTe的结合比与类似尺寸的CdSe纳米晶体的结合更弱。提出较弱的结合是由于重构的CdTe表面的极性较低和稳定性更高。

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