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Synthesis of relatively monodisperse ZnO nanocrystals from a precursor zinc 2,4-pentanedionate

机译:由前体2,4-戊二酮酸锌合成相对单分散的ZnO纳米晶体

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Monodisperse ZnO nanoparticles were successfully prepared through the decomposition of zinc acetylacetonate precursor in oleylamine. The samples were characterized by transmission electron microscope, X-ray diffraction and infrared spectroscopy. The particle size and morphology could be modified through tuning the reaction temperature, reaction period and concentration of zinc acetylacetonate. The grain size of monodisperse ZnO could be obtained at 205 and 300℃ for 1 h with 1:100 molar ratio of acetylacetonate and oleylamine, respectively. The average grain size of ZnO nanoparticles increased and the shape of ZnO particles varied with the reaction period prolonging or reaction temperature increasing. Some ZnO particles had self-aggregated into a belt using a solution of 1:10 molar ratio of zinc acetylacetonate and oleylamine at 250℃ for 1 h. The oleylamine plays an important role in preventing aggregation of ZnO nanoparticles.
机译:通过乙酰丙酮锌锌前驱体在油胺中的分解,成功制备了单分散的ZnO纳米颗粒。通过透射电子显微镜,X射线衍射和红外光谱对样品进行表征。可以通过调节反应温度,反应时间和乙酰丙酮锌的浓度来改变粒径和形貌。 ZnO的单分散粒径为205:300,乙酰丙酮和油胺的摩尔比为1:100,分别可获得1h。随着反应时间的延长或反应温度的升高,ZnO纳米颗粒的平均粒径增加,ZnO颗粒的形状发生变化。在250℃下,使用乙酰丙酮锌和油胺的摩尔比为1:10的溶液,一些ZnO颗粒已经自动聚集成带状,并保持了1 h。油胺在防止ZnO纳米颗粒聚集中起重要作用。

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