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An efficient method for the synthesis of nickel phosphide nanocrystals via thermal decomposition of single-source precursors

机译:通过热分解单源前体的热分解合成磷化镍纳米晶体的一种有效方法

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摘要

An efficient method was developed for the synthesis of nickel phosphide nanocrystals (NCs) via thermal decomposition of bis(triphenylphosphine) nickel dichloride (BTND) precursor in the presence of oleylamine (OAm) for the first time. The effect of synthetic conditions such as reaction temperature, reaction time and OAm quantity on the size and phase of the as-synthesized nickel phosphide NCs was discussed. The structure and morphology were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and N-2 adsorption-desorption measurements. The results showed that the size of Ni2P NCs can be controlled by increasing reaction temperature and OAm quantity. The phase of nickel phosphide NCs can be controlled by changing the reaction time. The shorter reaction time was beneficial for forming Ni12P5 NCs, and longer reaction time was beneficial for forming Ni2P NCs. Furthermore, a possible growth mechanism of the as-synthesized nickel phosphide NCs was proposed. These synthetic techniques may be expanded to other metal phosphide materials.
机译:首次通过BIS(三苯基膦)镍二氯化镍二氯化镍(BTND)前体的热分解在oleylamine(OAM)存在下,开发了一种有效的方法。讨论了合成条件如反应温度,反应时间和OAM数量对合成镍磷化物NCS的尺寸和相的影响。结构和形态的特征在于X射线衍射(XRD),透射电子显微镜(TEM),X射线光电子能谱(XPS)和N-2吸附 - 解吸测量。结果表明,通过增加反应温度和OAM量,可以控制Ni2P NCS的尺寸。可以通过改变反应时间来控制磷化镍NCS的相。较短的反应时间是有益于形成Ni12P5 NCS的有益,并且更长的反应时间有利于形成Ni2P NCS。此外,提出了一种如合成的磷化镍NCS的可能生长机制。这些合成技术可以扩展到其他金属磷化物材料。

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  • 来源
    《RSC Advances》 |2015年第16期|共8页
  • 作者单位

    China Univ Petr State Key Lab Heavy Oil Proc Key Lab Catalysis China Natl Petr Corp CNPC Qingdao 266580 Shandong Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Key Lab Catalysis China Natl Petr Corp CNPC Qingdao 266580 Shandong Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Key Lab Catalysis China Natl Petr Corp CNPC Qingdao 266580 Shandong Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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