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A study of novel eco-friendly nanomaterials for optoelectronic and electrochemical applications.

机译:用于光电和电化学应用的新型环保纳米材料的研究。

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摘要

Nanotechnology has developed rapidly in recent decades, producing many new functional materials, devices, and systems by controlling matter at nanometer length scales (1-100 nm). Nanocrystals are of broad interest due to their tunable size- and shape-dependent physical and chemical properties, which give them enormous potential for application in future electronics, renewable energy technologies, health care, and medicine. This dissertation focuses on understanding bottom-up synthesis of nanomaterials from molecular precursors. Through systematic controlled synthesis of nanomaterials, their properties can be tuned to meet the needs of specific applications. These studies also improve our overall understanding of the relationships between nanomaterial synthesis processes and the resulting product properties.;In chapter 1, we focus on copper-based alloy chalcogenide nanocrystals, particularly cation deficient nanocrystals that exhibit localized surface plasmon resonance (LSPR). This class of materials has attracted much interest due to their lack of toxicity, potential low cost, and tunable band gap and LSPR energies. Three specific systems are considered in this chapter. We present new methods for solution phase synthesis of Cu-In-S, Cu-Sn-S and Cu-Sn-Se and characterize the range of obtainable nanocrystal sizes, compositions, morphologies, and properties in each case. These materials have enormous potential for application in future low-cost solution-processed electronics and optoelectronics.;In chapter 2, we use cation exchange to prepare a new heterogeneous nanostructure. We employ cation-deficient copper sulfide (Cu2-xS) NCs as a template for preparing gold sulfide (Au2S) NCs. Such high-quality colloidal Au2S NCs are difficult to prepare directly. In this process, Au cations simultaneously diffuse into the NCs and fill Cu vacancies, as the original cations Cu diffuse out, initially forming Cu2- xS--Au2S core/shell nanostructures and then pure Au2S nanoparticles.;In chapter 3, we explore the use of degenerately doped copper chalcogenide NCs as electrocatalysts. Covellite phase Cu2-xS nanoplates with three different doping levels were tested for their electrocatalytic activity for the oxygen reduction reaction (ORR) in alkaline solution. Additionally, the most heavily doped, and most active, Cu2-xS nanoplates were deposited on carbon black and on reduced graphene oxide, producing significant improvement in electrical conductivity and electrocatalytic performance. This work showed that free hole-rich copper-deficient copper chalcogenides may provide a new opportunity to develop novel electrocatalysts and can be the starting point for a new class of nonprecious metal electrocatalysts.;In chapter 4, we study highly graphitized nitrogen-doped nanocarbon materials derived from low-cost nitrogen-carbon precursors via a high-temperature approach in the presence of Fe, Co, Ni, and Mn. Synthesis in the presence of Fe yielded the largest tube size, followed by Co and Ni. In contrast to generating tubes, Mn produced a clot-like carbon morphology with relatively low surface area. We tested the ORR activity of these nanocarbons in both acidic and alkaline media, and demonstrated that the Fe-derived tubes exhibited the highest electrocatalytic activity, along with the highest BET surface area, electrochemically accessible surface area, and nitrogen content. This work provides an effective approach to further improve the performance of M-N-C precious metal-free electrocatalysts by optimizing morphology and surface area of nanocarbons.;Chapter 5 provides a summary of the dissertation and chapter 6 discusses possible future research directions.
机译:纳米技术在最近的几十年中发展迅速,通过控制纳米尺度(1-100 nm)的物质,生产了许多新的功能材料,设备和系统。纳米晶体因其可调节的尺寸和形状相关的物理和化学特性而备受关注,这使其在未来的电子,可再生能源技术,医疗保健和医学中具有巨大的应用潜力。本论文着重于了解从分子前驱物自下而上合成纳米材料。通过系统地控制合成纳米材料,可以调整其性能以满足特定应用的需求。这些研究还提高了我们对纳米材料合成过程与所得产品性能之间关系的整体理解。在第一章中,我们重点研究铜基合金硫族化物纳米晶体,特别是表现出局部表面等离子体激元共振(LSPR)的阳离子缺陷型纳米晶体。这类材料因缺乏毒性,潜在的低成本以及可调节的带隙和LSPR能量而引起了人们的极大兴趣。本章考虑了三种特定的系统。我们提出了Cu-In-S,Cu-Sn-S和Cu-Sn-Se固溶相合成的新方法,并描述了每种情况下可获得的纳米晶体尺寸,组成,形态和性质的范围。这些材料在未来低成本溶液加工的电子和光电子学中具有巨大的应用潜力。在第二章中,我们使用阳离子交换来制备新的异质纳米结构。我们采用阳离子不足的硫化铜(Cu2-xS)NC作为制备硫化金(Au2S)NC的模板。这种高质量的胶态Au2S NCs很难直接制备。在此过程中,Au阳离子同时扩散到NC中并填充Cu空位,因为原始阳离子Cu扩散出来,最初形成Cu2-xS--Au2S核/壳纳米结构,然后形成纯Au2S纳米颗粒。;在第3章中,我们探索了简并掺杂的硫族硫化铜NCs作为电催化剂。测试了具有三种不同掺杂水平的Covellite相Cu2-xS纳米板对碱性溶液中氧还原反应(ORR)的电催化活性。此外,掺杂最重,活性最高的Cu2-xS纳米板沉积在炭黑和还原的氧化石墨烯上,从而显着提高了电导率和电催化性能。这项工作表明,富空孔的缺铜的铜硫属元素化物可能为开发新型电催化剂提供新的机会,并且可以成为新型非贵金属电催化剂的起点。在第四章​​中,我们研究了高度石墨化的氮掺杂纳米碳。在Fe,Co,Ni和Mn存在的情况下,通过高温方法从低成本的氮碳前体中提取的金属材料。在Fe的存在下合成产生最大的管尺寸,然后是Co和Ni。与发电管相反,锰产生的凝块状碳形态具有相对较低的表面积。我们在酸性和碱性介质中测试了这些纳米碳的ORR活性,并证明了铁衍生的管表现出最高的电催化活性,以及​​最高的BET表面积,电化学可及的表面积和氮含量。这项工作为通过优化纳米碳的形态和表面积,进一步提高M-N-C不含金属的电催化剂的性能提供了有效的方法。第五章对全文进行了总结,第六章探讨了未来可能的研究方向。

著录项

  • 作者

    Wang, Xianliang.;

  • 作者单位

    State University of New York at Buffalo.;

  • 授予单位 State University of New York at Buffalo.;
  • 学科 Engineering.;Materials science.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 149 p.
  • 总页数 149
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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