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Structural and Functional Properties of Iron (Ⅱ, Ⅲ)-Doped ZnO Monodisperse Nanoparticles Synthesized by Polyol Method

机译:多元醇法合成铁(Ⅱ,Ⅲ)掺杂的ZnO单分散纳米粒子的结构和功能性能

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In this work, bare and (Fe~(3+) and Fe~(2+))-doped ZnO nanoparticles (NPs) have been synthesized in a polyol medium at 180℃. The synthesis in polyol allows a precise control of doping under size-controlled conditions. The Fe concentration varied in the 0-2 at. % range. As-synthesized samples were characterized by X-ray diffraction (XRD), Fourier Transform Infrared (FT-IR), Photoluminescence (PL) spectroscopy and Vibrational Sample Magnetometry (VSM). XRD measurements confirmed the formation of well crystallized wurtzite ZnO with absence of secondary phases in bare and doped samples; the average crystallite size was estimated at 8.4 ± 0.3 nm for bare ZnO NPs. Systematic shifts in the main diffraction peaks due to the incorporation of the dopant species were observed in the Fe~(3+) and Fe~(2+) doped-ZnO samples. FT-IR analyses evidenced the presence of organic moieties on the surface of the nanoparticles that are associated to the functional groups of polyol by-products; these adsorbed species could explain the observed stability of the NPs when suspended in water. PL measurements (excitation wavelength 345 nm) reveled that a tuning in the emission bands of ZnO NPs can be achieved through doping. VSM measurements evidenced a weak but noticeable ferromagnetic response at room temperature (RT) in doped samples.
机译:在这项工作中,已在180℃的多元醇介质中合成了裸露的和(Fe〜(3+)和Fe〜(2+))掺杂的ZnO纳米粒子(NPs)。多元醇中的合成可以在尺寸受控的条件下精确控制掺杂。铁的浓度在0-2at。之间变化。 % 范围。合成后的样品通过X射线衍射(XRD),傅立叶变换红外(FT-IR),光致发光(PL)光谱和振动样品磁强(VSM)进行表征。 XRD测量证实了裸露和掺杂样品中结晶良好的纤锌矿型ZnO的形成,没有次级相。裸露的ZnO NP的平均微晶尺寸估计为8.4±0.3 nm。在Fe〜(3+)和Fe〜(2+)掺杂的ZnO样品中观察到由于掺入了掺杂物而导致的主要衍射峰发生了系统移动。 FT-IR分析表明,在纳米颗粒表面上存在与多元醇副产物的官能团相关的有机部分。这些吸附的物质可以解释NPs悬浮在水中时观察到的稳定性。 PL测量(激发波长345 nm)表明,可以通过掺杂实现ZnO NPs发射带的调谐。 VSM测量表明,在室温(RT)下,掺杂样品中的铁磁响应较弱但很明显。

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