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Synthesis, structure and electronic properties of ultranarrow CdS nanorods

机译:超窄CdS纳米棒的合成,结构和电子性能

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We report on the one-step synthesis of ultra narrow wurtzite CdS nanorods using bench top chemical decomposition route. The synthesized CdS nanorods are of 1.8 nm in diameter and show major confinement along the radial dimension, which is well below the exciton Bohr radius of bulk CdS (2.5 nm). Structural and self-assembly properties of nanorods are studied using X-ray Diffraction (XRD) and small angle X-ray scattering (SAXS) measurements, which reveal preferred orientation of the nanorods along direction with 2D supercrystalline spatial distribution. The estimated nanorod dimensions from XRD is corroborated with the transmission electron microscopy observations. UV–vis and photoluminescence spectroscopy reveals significant increase in the band gap in comparison to bulk CdS which is further tallied with the simulations using effective mass approximation (EMA). Formation of discrete structure of valence band and conduction band due to strongly quantum confined excitons in the radial direction is evidenced from EMA simulation. Combination of experimental and theoretical approach helps in understanding the structure–property relationship for ultranarrow CdS rods which might lead to nanorod based applications.
机译:我们报告使用台式化学分解路线的一步法合成超窄纤锌矿CdS纳米棒。合成的CdS纳米棒的直径为1.8 nm,并且沿径向方向显示主要限制,远低于本体CdS的激子玻尔半径(2.5 nm)。使用X射线衍射(XRD)和小角度X射线散射(SAXS)测量研究了纳米棒的结构和自组装特性,这些揭示了纳米棒沿2D超晶空间分布方向的优选方向。 XRD估计的纳米棒尺寸与透射电子显微镜观察结果相符。紫外可见光谱和光致发光光谱显示,与大体积CdS相比,带隙显着增加,这在使用有效质量近似(EMA)的模拟中得到了进一步证实。 EMA模拟证明了径向上强量子限制激子引起的价带和导带离散结构的形成。实验方法和理论方法的结合有助于理解超窄CdS棒的结构-性质关系,这可能会导致基于纳米棒的应用。

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