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Advanced transition metal phosphide materials from single-source molecular precursors.

机译:来自单一来源分子前体的先进过渡金属磷化物材料。

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摘要

In this thesis, the feasibility of employing organometallic single-source precursors in the preparation of advanced transition metal pnictide materials such as colloidal nanoparticles and films has been investigated. In particular, the ternary FeMnP phase was targeted as a model for preparing advanced heterobimetallic phosphide materials, and the iron-rich Fe3P phase was targeted due to its favorable ferromagnetic properties as well as the fact that the preparation of advanced Fe3P materials has been elusive by commonly used methods.;Progress towards the synthesis of advanced Fe2--xMn xP nanomaterials and films was facilitated by the synthesis of the novel heterobimetallic complexes FeMn(CO)8(mu-PR1R 2) (R1 = H, R2 = H or R1 = H, R2 = Ph), which contain the relatively rare mu-PH2 and mu-PPhH functionalities. Iron rich Fe2--xMnxP nanoparticles were obtained by thermal decomposition of FeMn(CO)8(mu-PH 2) using solution-based synthetic methods, and empirical evidence suggested that oleic acid was responsible for manganese depletion. Films containing Fe, Mn, and P with the desired stoichiometric ratio of 1:1:1 were prepared using FeMn(CO)8(mu-PH2) in a simple low-pressure metal-organic chemical vapor deposition (MOCVD) apparatus. Although the elemental composition of the precursor was conserved in the deposited film material, spectroscopic evidence indicated that the films were not composed of pure-phase FeMnP, but were actually mixtures of crystalline FeMnP and amorphous FeP and Mn xOy.;A new method for the preparation of phase-pure ferromagnetic Fe 3P films on quartz substrates has also been developed. This approach involved the thermal decomposition of the single-source precursors H 2Fe3(CO)9PR (R = tBu or Ph) at 400 °C. The films were deposited using a simple home-built MOCVD apparatus and were characterized using a variety of analytical methods. The films exhibited excellent phase purity, as evidenced by X-ray diffraction, X-ray photoelectron spectroscopy, and field-dependent magnetization measurements, the results of which were all in good agreement with measurements obtained from bulk Fe3P. As-deposited Fe3P films were found to be amorphous, and little or no magnetic hysteresis was observed in plots of magnetization versus applied field. Annealing the Fe3P films at 550 °C resulted in improved crystallinity as well as the observation of magnetic hysteresis.
机译:本文研究了有机金属单源前驱体在制备先进的过渡金属肽材料如胶体纳米颗粒和薄膜中的可行性。特别是,以三元FeMnP相为模型来制备高级异双金属磷化物材料,并以富铁的Fe3P相为目标,这是由于其良好的铁磁性能以及先进的Fe3P材料的制备难以实现的事实。新型异质双金属配合物FeMn(CO)8(mu-PR1R 2)(R1 = H,R2 = H或R1)的合成促进了高级Fe2--xMn xP纳米材料和薄膜的合成= H,R2 = Ph),其中包含相对罕见的mu-PH2和mu-PPhH功能。富铁的Fe2--xMnxP纳米粒子是通过使用溶液基合成方法对FeMn(CO)8(mu-PH 2)进行热分解而获得的,经验证据表明油酸是造成锰消耗的原因。在简单的低压金属有机化学气相沉积(MOCVD)设备中,使用FeMn(CO)8(mu-PH2)制备具有所需化学计量比为1:1:1的含Fe,Mn和P的薄膜。尽管在沉积的薄膜材料中保留了前体的元素组成,但光谱证据表明该薄膜不是由纯相FeMnP组成,而是实际上是结晶FeMnP和非晶态FeP和Mn xOy的混合物。还已经开发了在石英衬底上制备纯铁磁Fe 3P薄膜的方法。这种方法涉及在400°C下热分解单源前驱体H 2Fe3(CO)9PR(R = tBu或Ph)。使用简单的家用MOCVD设备沉积薄膜,并使用多种分析方法对其进行表征。 X射线衍射,X射线光电子能谱和与场有关的磁化强度测量结果表明,这些膜具有极好的相纯度,其结果与从大量Fe3P获得的测量结果非常吻合。发现沉积的Fe3P薄膜是非晶态的,在磁化强度与外加磁场的关系图中几乎没有或没有观察到磁滞现象。将Fe3P薄膜在550°C退火可改善结晶度并观察磁滞现象。

著录项

  • 作者

    Colson, Adam Caleb.;

  • 作者单位

    Rice University.;

  • 授予单位 Rice University.;
  • 学科 Chemistry General.;Engineering Materials Science.;Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 184 p.
  • 总页数 184
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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