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Unconventional Strategies Toward Efficient Self-Assembly in Solution Processed Small Molecule Organic Photovoltaics

机译:在溶液加工的小分子有机光伏中实现高效自组装的非常规策略

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摘要

Broadly described by conductive ?-conjugated cores with electronically-inert solubilizing groups, solution-processed organic semiconductors have wide applications in modern electronics such as transistor, sensor, lighting and energy-harvesting technologies. However, their optical and electronic properties in the solid-state strongly depend upon their ability to organize into ordered phases during solution deposition. Frustrated self-assembly contributes to performance variation and thermal instability. Organic photovoltaics (OPVs) offer a relevant case-in-point, as they rely on a blend of electron-donating and electron-accepting semiconductors to achieve light harvesting and photocurrent generation. Efficient charge generation requires the self-assembly of internal ordered domains and broad interfaces between these components, while charge carrier extraction simultaneously demands that each form continuous pathways. Understanding how the chemical structure and processing of these materials impacts their organizational tendencies is essential for the design of materials that readily and reliably reach this desired complex morphology.;This dissertation discusses the novel strategies for directing self-assembly in OPV materials suggested by this understanding. Chapter 1 presents our current understanding of the processes involved in the formation of the bulk heterojunction and processing methods for manipulating morphology, such as solvent additives. Chapter 2 discusses how a solid and electronically-inert additive, polystyrene, provides additional interfaces for crystalline nucleation during solution-casting, a different mechanism than solvent additives. In Chapter 3, we find that molecular design that reduces available structural conformation decreases morphological disorder during solution-deposition, with minimal impact on other molecular properties. Chapter 4 discusses how molecules designed to change topology in solution and film states can readily create ordered phases without sacrificing processibility. Chapter 5 concludes this work by discussing how these strategies can be applied toward emerging fields within organic semiconductor research, namely processing from environmentally-friendly solvents and designing of electron-accepting materials.
机译:溶液处理有机半导体广泛地描述为具有电子惰性增溶基团的导电α共轭核,在现代电子技术中具有广泛的应用,例如晶体管,传感器,照明和能量收集技术。然而,它们在固态中的光学和电子性质在很大程度上取决于它们在溶液沉积过程中组织成有序相的能力。沮丧的自组装会导致性能变化和热不稳定。有机光伏(OPV)提供了一个相关的案例,因为它们依靠给电子和受电子半导体的混合物来实现光收集和光电流产生。高效的电荷产生需要内部有序域的自组装和这些组件之间的广泛接口,而电荷载流子提取同时要求它们形成连续的路径。理解这些材料的化学结构和加工过程如何影响其组织趋势,对于设计能够轻松,可靠地达到所需的复杂形态的材料至关重要。;本文讨论了这种理解所提出的指导自组装在OPV材料中的新颖策略。 。第1章介绍了我们目前对本体异质结形成的过程以及用于处理形态学(例如溶剂添加剂)的加工方法的理解。第2章讨论了固态和电子惰性添加剂聚苯乙烯如何为溶液浇铸过程中的晶核形成提供额外的界面,这种机理与溶剂添加剂不同。在第3章中,我们发现减少可用结构构象的分子设计可减少溶液沉积过程中的形态紊乱,而对其他分子特性的影响则最小。第4章讨论了旨在改变溶液和薄膜状态的拓扑结构的分子如何在不牺牲可加工性的情况下轻松创建有序相。第5章通过讨论如何将这些策略应用于有机半导体研究中的新兴领域(即从环境友好的溶剂中进行处理和设计电子接受材料)来结束这项工作。

著录项

  • 作者

    McDowell, Caitlin Irene.;

  • 作者单位

    University of California, Santa Barbara.;

  • 授予单位 University of California, Santa Barbara.;
  • 学科 Materials science.;Chemistry.
  • 学位 Ph.D.
  • 年度 2018
  • 页码 207 p.
  • 总页数 207
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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