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Self-assembly of colloidal nanocrystals: Surface ligands promote the formation of unexpected superlattices.

机译:胶体纳米晶体的自组装:表面配体促进意外的超晶格的形成。

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摘要

The advent and refinement of chemical techniques to produce uniform collections of colloidal nanocrystals in recent years has made accessible a wide range of nanocrystal materials, shapes, and sizes, offering a fertile testbed for developing an understanding of nanoscale crystallization. Elucidating the role of nanocrystal surfaces in promoting self-assembly of superlattice phases unanticipated by hard-shape packing models has been the focus of my graduate work. Chapter One provides a practical overview of the experimental approaches to prepare and characterize colloidal nanocrystals and self-assembled nanocrystal superlattices. Chapter Two discusses colloidal nanocrystal surfaces including atomic composition, chemical reactivity, and influence over electronic structure. Chapter Three provides an overview of nanocrystal self-assembly including interparticle potentials and predicted phase behavior for hard and soft shapes. Chapter Four describes the preparation of tetrahedrally-shaped CdSe nanocrystals and their self-assembly into an unexpected superlattice structure. Chapter Five presents a selection of electron microscopy images of superlattices comprised of nearly spherical nanocrystals. Chapter Six describes the application of image analysis techniques to elucidate ligand shell deformability of spherical nanocrystals and resulting implications for entropy-driven crystallization of soft objects. Chapter Seven analyzes the role of PbS surface ligand desorption in determining binary phase behavior with Au nanocrystals. Chapter Eight describes the implications of the ideas presented in this thesis, places them in the context of recent work by others in the field, and offers an outlook towards promising directions for future research. Together, the ideas contained herein aim to provide the conceptual foundation necessary to exploit nanocrystal self-assembly for the rational design of next-generation functional solids.
机译:近年来,化学技术的出现和改进以产生均匀的胶体纳米晶体集合,已经使人们可以使用各种各样的纳米晶体材料,形状和大小,从而为发展对纳米级结晶的理解提供了肥沃的试验台。阐明纳米晶体表面在促进硬形堆积模型无法预料的超晶格相自组装中的作用一直是我研究工作的重点。第一章概述了制备和表征胶体纳米晶体和自组装纳米晶体超晶格的实验方法。第二章讨论了胶体纳米晶体的表面,包括原子组成,化学反应性和对电子结构的影响。第三章概述了纳米晶体的自组装,包括颗粒间的电势以及硬和软形状的预测相行为。第四章介绍了四面体形CdSe纳米晶体的制备及其自组装成意想不到的超晶格结构。第五章介绍了由近球形纳米晶体组成的超晶格的电子显微镜图像。第六章介绍了图像分析技术在阐明球形纳米晶体的配体壳可变形性方面的应用,以及由此产生的熵驱动软物体结晶的含义。第七章分析了PbS表面配体解吸在确定Au纳米晶体的二元相行为中的作用。第八章介绍了本文提出的思想的含义,将其置于本领域其他人最近的工作背景下,并展望了未来研究的有希望的方向。总之,本文包含的思想旨在提供必要的概念基础,以开发纳米晶体自组装用于下一代功能性固体的合理设计。

著录项

  • 作者

    Boles, Michael Adam.;

  • 作者单位

    The University of Chicago.;

  • 授予单位 The University of Chicago.;
  • 学科 Physical chemistry.;Nanoscience.
  • 学位 Ph.D.
  • 年度 2016
  • 页码 247 p.
  • 总页数 247
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 宗教;
  • 关键词

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