首页> 外文学位 >Synthesis and characterization of anisotropic cadmium and lead sulfide nanostructures from single source molecular precursors and an insight to their growth mechanisms.
【24h】

Synthesis and characterization of anisotropic cadmium and lead sulfide nanostructures from single source molecular precursors and an insight to their growth mechanisms.

机译:从单一来源的分子前体合成和表征各向异性的镉和硫化铅纳米结构,并了解其生长机理。

获取原文
获取原文并翻译 | 示例

摘要

This thesis details the synthesis and characterization of anisotropic cadmium and lead sulfide nanostructures from single-source molecular precursors. Six new precursors were synthesized for cadmium and lead sulfide each, by the reaction of the appropriate metal acetate with picolinic (HPic), 2,6-dipicolinic (H2dipic) or salicylic acid (H2sal) followed by the addition of thiourea (th) or thiosemicarbazide (ths). The precursors for CdS are [Cd(Hsal)2(tu)2] (Cd1a), [Cd(Hsal) 2(ths)2]·nH2O (Cd1b), [Cd(pic) 2(tu)2]·0.5H2O (Cd2a), [Cd(pic) 2(ths)2]·2H2O (Cd2b), [Cd(dipic)(tu) 2] (Cd3a) and [Cd(dipic)(ths)2(H2O)]·2H 2O (Cd3b) and the precursors for PbS are [Pb(Hsal) 2(th)2] (Pb1a), [Pb(Hsal)2(ths) 2] (Pb1b), [Pb(pic)2(th)2] ( Pb2a), [Pb(pic)2(ths)2] (Pb2b), [Pb(dipic)(th)(H2O)]2·2H2O ( Pb3a) and [Pb(dipic)(ths)2]·H2O ( Pb3b). All of the compounds were characterized spectroscopically and by elemental analysis. Cd1a, Cd2a, Cd2b, Cd3a, Cd3b, Pb2b Pb3a and Pb3b formed well-defined crystals and were characterized by single crystal X-ray diffraction.;The precursors were decomposed at or around 170 °C using n-cetyltrimethylammonium bromide (CTAB), sodium dodecylsulphate (SDS), ethylenediamine, oleic acid, oleylamine, trioctylamine or hexadecylamine as surfactants. Systematic variations of surfactants gave small spherical nanoparticles, micro-sized flowers, multipods and nanorods for CdS and nanocubes, truncated nanocubes, hexapods, octahedrons and dendritic stars for PbS. From XRPD studies it was found that most of the CdS nanostructures were of the stable hexagonal phase. However, in two cases the nanostructures were found to be predominantly of a metastable orthorhombic phase. For PbS system, all the decompositions yielded pure crystalline galena. For CdS system, TEM studies revealed planar defects (such as polysynthetic and multiplet twinning) in the nanocrystals, which gave an explanation for mechanism of growth. For PbS system, in order to elucidate the effect of single source precursors on the mechanism of growth of nanoparticles, the decomposition results were compared with PbS nanostructures synthesized from multiple-source precursors, lead acetate and thiourea or thiosemicarbazide. It was found that in the reactions of multiple source precursors, acidic components in the reaction mixture (oleic acid, acetic acid) led to etching and crystal splitting, which played a crucial role in the formation of anisotropic nanostructures.
机译:本文详细介绍了单源分子前驱体的各向异性镉和硫化铅纳米结构的合成与表征。通过使适当的金属乙酸盐与吡啶甲酸(HPic),2,6-二吡啶甲酸(H2dipic)或水杨酸(H2sal)反应,然后添加硫脲(th)或苯甲酸,分别合成了六种新的镉和硫化铅前体。硫代氨基脲(ths)。 CdS的前体是[Cd(Hsal)2(tu)2](Cd1a),[Cd(Hsal)2(ths)2]·nH2O(Cd1b),[Cd(pic)2(tu)2]·0.5 H2O(Cd2a),[Cd(pic)2(ths)2]·2H2O(Cd2b),[Cd(dipic)(tu)2](Cd3a)和[Cd(dipic)(ths)2(H2O)]· 2H 2O(Cd3b)和PbS的前体是[Pb(Hsal)2(th)2](Pb1a),[Pb(Hsal)2(ths)2](Pb1b),[Pb(pic)2(th) 2](Pb2a),[Pb(pic)2(ths)2](Pb2b),[Pb(dipic)(th)(H2O)] 2·2H2O(Pb3a)和[Pb(dipic)(ths)2] ·H2O(Pb3b)。所有化合物均通过光谱和元素分析进行​​表征。 Cd1a,Cd2a,Cd2b,Cd3a,Cd3b,Pb2b,Pb3a和Pb3b形成了明确的晶体,并通过单晶X射线衍射进行了表征;前驱物在170°C左右或使用正十六烷基三甲基溴化铵(CTAB)分解,十二烷基硫酸钠(SDS),乙二胺,油酸,油胺,三辛胺或十六烷基胺作为表面活性剂。表面活性剂的系统变化产生了小的球形纳米颗粒,用于CdS和纳米立方体的微细花,多荚和纳米棒,用于PbS的截短的纳米立方体,六足类,八面体和树枝状星。通过XRPD研究发现,大多数CdS纳米结构均具有稳定的六方相。然而,在两种情况下,发现纳米结构主要为亚稳态斜方晶相。对于PbS系统,所有分解均产生纯净的方铅矿。对于CdS系统,TEM研究揭示了纳米晶体中的平面缺陷(例如多合成和多重孪晶),这为生长机理提供了解释。对于PbS系统,为了阐明单源前体对纳米颗粒生长机理的影响,将分解结果与多源前体,乙酸铅和硫脲或硫代氨基脲合成的PbS纳米结构进行了比较。发现在多种来源的前体的反应中,反应混合物中的酸性成分(油酸,乙酸)导致蚀刻和晶体分裂,这在各向异性纳米结构的形成中起着至关重要的作用。

著录项

  • 作者

    Mandal, Trinanjana.;

  • 作者单位

    Rice University.;

  • 授予单位 Rice University.;
  • 学科 Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 119 p.
  • 总页数 119
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号