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Synthesis of trimetallic nitride endohedral metallofullerene derivatives for enhanced solar energy conversion.

机译:合成三金属氮化物内表面金属富勒烯衍生物以增强太阳能转化。

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摘要

The preparation and electrochemical properties of donor – acceptor systems based on trimetallic nitride endohedral metallofullerenes (TNT-EMFs) for enhanced solar energy conversion is described. It was found that TNT-EMFs have an enhanced ability to stabilize charge separated states formed upon light irradiation when compared to empty cage fullerene analogues. The influence of the linker connecting the donor and acceptor moieties was studied in two different systems. Optimal conditions for preparing cyclopropanated Bingel-Hirsch derivaties of the most common TNT-EMFs were found; this functionalization approach is a very useful alternative to the 1,3-dipolar cycloaddition reactions that yield pyrrolidine derivatives, because the latter are sensitive to both heat and oxidation.;Novel D-A systems were prepared using this strategy and their electrochemical properties revealed that they form films by electro-oxidative polymerization. These films generate current under irradiation. Finally, the arcing conditions for the preparation of a novel sulfur endohedral metallofullerene family were optimized and their electrochemical properties were studied. Due to the high yields obtained, these new endohedral compounds may also be potential candidates to be used in similar applications to those found for other TNT-EMFs.
机译:描述了基于三金属氮化物内表面金属富勒烯(TNT-EMFs)的供体-受体体系的制备及其电化学性能,可提高太阳能转化率。发现与空笼式富勒烯类似物相比,TNT-EMF具有增强的稳定由光照射形成的电荷分离状态的能力。在两个不同的系统中研究了连接供体和受体部分的接头的影响。发现了最常见的TNT-EMFs制备环丙烷化的Bingel-Hirsch衍生物的最佳条件。这种官能化方法是产生吡咯烷衍生物的1,3-偶极环加成反应的非常有用的替代方法,因为后者对热和氧化均敏感。;新颖的DA系统是用这种策略制备的,其电化学性质表明它们形成了膜通过电氧化聚合。这些膜在辐射下产生电流。最后,优化了制备新型硫内表面金属富勒烯家族的电弧条件,并研究了它们的电化学性能。由于获得的高收率,这些新的内面体化合物也可能是潜在的候选物,可用于与其他TNT-EMF相似的应用中。

著录项

  • 作者

    Pinzon Joya, Julio Roberto.;

  • 作者单位

    Clemson University.;

  • 授予单位 Clemson University.;
  • 学科 Alternative Energy.;Chemistry Inorganic.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 205 p.
  • 总页数 205
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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