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Ni(II) and Pb(II) dithiocarbamate complexes as precursors for the synthesis of HDA-capped NiS and PbS nanoparticles

机译:Ni(II)和pb(II)二硫代氨基甲酸盐配合物作为合成HDa封端的Nis和pbs纳米颗粒的前体

摘要

Ni(II) and Pb(II) dithiocarbamate complexes were synthesized and characterized by elemental analysis, UV-Vis, FTIR and TGA and some of the Ni(II) complexes and one Pb(II) were further analyzed by 1H-NMR and 13C-NMR spectroscopy. Generally all the dithiocarbamate ligands are soluble in water while the complexes were soluble mostly in solvents such as chloroform, toluene, DMSO and DCM. Based on the elemental analysis, the dithiocarbamate complexes are formulated as four coordinate (tetrahedral or square planar) compounds. However, the FTIR showed that each of the dithiocarbamate ligands acted as bidentate ligand through two sulfur atoms. The TGA of the most complexes showed one major decomposition step to give respective metal sulfide above 200 oC. In this research project, dithiocarbamate complexes were used as single source precursor for the synthesis of metal sulfide nanoparticles. We studied the optical and structural properties of metal sulfide nanoparticles using UV-Vis, photoluminescence (PL), powder X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The absorption spectra of the metal sulfide nanoparticles are blue shifted in respect to bulk material and they also showed broad emission. The XRD of the NiS nanoparticles were indexed to the cubic and rhombohedral phase, with crystallite sizes of 15 - 18 nm. The XRD of PbS nanoparticles were indexed to the face centered cubic and cubic rock salts, with the crystallite sizes 12 - 18 nm. The TEM images of the metal sulfide nanoparticles showed particles with spherical and rectangular shapes with crystallite sizes 4 - 35 nm.
机译:合成了Ni(II)和Pb(II)二硫代氨基甲酸酯配合物并通过元素分析对其进行了表征,并通过1H-NMR和13C对UV-Vis,FTIR和TGA以及一些Ni(II)配合物和一种Pb(II)进行了进一步分析。 -NMR光谱。通常,所有二硫代氨基甲酸酯配体都可溶于水,而络合物则大部分可溶于溶剂,如氯仿,甲苯,DMSO和DCM。根据元素分析,将二硫代氨基甲酸酯配合物配制成四个配位(四面体或正方形平面)化合物。然而,FTIR显示,每个二硫代氨基甲酸酯配体通过两个硫原子充当二齿配体。大多数配合物的TGA显示出一个主要的分解步骤,从而使各自的金属硫化物高于200 oC。在该研究项目中,二硫代氨基甲酸酯配合物被用作合成金属硫化物纳米粒子的单一来源前体。我们使用UV-Vis,光致发光(PL),粉末X射线衍射(XRD),能量色散X射线(EDX),扫描电子显微镜(SEM)和透射电子显微镜对金属硫化物纳米颗粒的光学和结构性质进行了研究( TEM)。相对于块状材料,金属硫化物纳米粒子的吸收光谱蓝移,并且它们还显示出宽发射。 NiS纳米粒子的XRD指示为立方相和菱面体相,微晶尺寸为15-18 nm。将PbS纳米粒子的XRD标记为面心立方和立方岩盐,微晶尺寸为12-18 nm。金属硫化物纳米粒子的TEM图像显示具有球形和矩形形状且微晶尺寸为4-35 nm的颗粒。

著录项

  • 作者

    Chintso Thobani;

  • 作者单位
  • 年度 2015
  • 总页数
  • 原文格式 PDF
  • 正文语种 English
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