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Novel high volumetric energy density nanostructured electrode materials for biomedical applications.

机译:用于生物医学应用的新型高体积能量密度纳米结构电极材料。

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摘要

A definitive focus is being made to develop cathode materials of higher energy and good power for primary and rechargeable lithium batteries upon the development of implantable biomedical devices (cardiac defibrillators). In this thesis, novel electroactive nanostructured silver metal oxyfluoride perovskites, Ag1+3Mo6+(O3F 3) and Ag1+3Nb5+(O2F 4) have been successfully synthesized by a mechanochemical reaction. The formation of these perovskites was investigated throughout the Ag-Mo / Nb composition range with the use of either Ag1+ or Ag 2+ in the form of AgF and AgF2 as the reactant, respectively. The compositional study combined with XRD and extensive Raman investigation was utilized to determine structure and cation distribution and infer oxidation state.;An electrochemical characterization of these silver metal oxyfluoride perovskite positive electrodes for Li batteries was investigated for the first time as a function of synthesis condition, stoichiometry and effect of Mo and Ag derived second phases. A detailed in-situ electrochemical study by XAS, Raman and XRD was performed, revealing a 3 electron silver displacement or conversion reaction at > 3 V and a 2 electron reduction of Mo6+ to Mo4+ in the region 3 V.;To further improve the rate capability of silver metal oxyfluorides, metallic Ag2F phase has been successfully synthesized through the mechanochemical reaction of Ag and AgF. Its unique metallic character within Ag layers lead to a very good electronic conductivity (7.89x10 -2 S/cm). The efficacy of SMOF composites consisting of conducting matrix (carbon black, Ag2F and Ag phase) for lithium battery was investigated through discharge rate studies. Results indicated that Ag 2F phase could be utilized as an alternative conductive additive with exceptional density.
机译:随着可植入生物医学设备(心脏除颤器)的发展,人们正集中精力开发用于一次和可充电锂电池的高能量和高功率的正极材料。本文通过机械化学反应成功地合成了新型电活性纳米结构的氟氧化钙金属银,即Ag1 + 3Mo6 +(O3F 3)和Ag1 + 3Nb5 +(O2F4)。在整个Ag-Mo / Nb组成范围内,分别使用AgF +和AgF2形式的Ag1 +或Ag 2+作为反应物,研究了这些钙钛矿的形成。结合XRD的成分研究和广泛的拉曼研究,确定结构和阳离子分布并推断氧化态。;首次研究了锂电池中这些金属氟氧化物钙钛矿型正极的电化学特性,作为合成条件的函数,化学计量以及Mo和Ag衍生的第二相的影响。 XAS,Raman和XRD进行了详细的原位电化学研究,揭示了在> 3 V时发生3电子银置换或转化反应,并且在<3 V区域中将Mo6 +还原为Mo4 +的2电子。通过Ag和AgF的机械化学反应已成功合成了金属氟氧化物的高速率容量,金属Ag2F相。其在Ag层中独特的金属特性导致非常好的电子传导性(7.89x10 -2 S / cm)。通过放电速率研究,研究了由导电基质(炭黑,Ag2F和Ag相)组成的SMOF复合材料对锂电池的功效。结果表明,Ag 2F相可以用作具有优异密度的替代导电添加剂。

著录项

  • 作者

    Tong, Wei.;

  • 作者单位

    Rutgers The State University of New Jersey - New Brunswick.;

  • 授予单位 Rutgers The State University of New Jersey - New Brunswick.;
  • 学科 Chemistry Inorganic.;Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 265 p.
  • 总页数 265
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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