Structure and properties of organic semiconductors: from single polymers and oligomers to interacting heterogeneous nanomaterials

有机半导体的结构和性能：从单一聚合物和低聚物到相互作用的异质纳米材料

• 批准号: RGPIN-2014-05986
• 负责人: Lagowski, Jolanta
• 金额: $ 1.82万
• 依托单位: Memorial University of Newfoundland
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2017
• 资助国家: 加拿大
• 起止时间: 2017-01-01 至 2018-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=633362
• 关键词: Structure; properties; organic; semiconductors; single

Materials made of organic conjugated polymers, oligomers and other carbon-based molecular systems are currently a subject of many intensive investigations because of their great potential in optoelectronics. Their applications have been demonstrated in devices such as solar cells, light-emitting diodes, transistors, integrated circuits, sensors, electro-chromic displays, optical switches, electro-optic modulators, batteries and others. It has been found that these devices perform best when they have multilayered and/or heterogeneous structures. For example, bulk heterojunction organic solar cells (where fullerenes, C60 or C70, are blended with the polymers or oligomers) give an improved performance due to a more balanced charge carrier transport. These experimental findings indicate that the weak intermolecular van der Waals (dispersion) forces play an important role in determining the (nanoscale) structures and, hence, properties of these heterogeneous organic semiconductors. Understanding the complex interactions between the building blocks of the organic semiconductors can lead to the design of novel materials. This understanding and the design of new materials is critically important for development of the next generation of organic optoelectronic applications. Using computational methods, the long term goal of my research program is to gain greater understanding of how the main components of the heterogeneous nano-filled organic composites interact and how these interactions eventually affect the materials’ overall electronic and optical properties. My group models the molecular systems as isolated chains, supramolecules, nanoclusters or solids. Our main theoretical/computational tool is density functional theory (DFT). We plan to use the various types of the dispersion corrected DFT to study the molecular structures of these systems. Time-dependent DFT (TD-DFT) is employed to study the excited states and the solid-state DFT is used to determine the polymer crystalline structures. We propose to study these systems in solutions as well as in vacuum (gas phase). This is because, even though the solvent is often removed in the final stage of the fabrication of a given material, there are numerous experimental indications (e.g. aggregate formations) that the type of solvent used in the fabrication process affects the performance of the device. The short-term objectives of my research involve the investigations of the industrially relevant (promising) organic heterogenous nano-complexes using the dispersion corrected DFT and TD-DFT with and without the presence of solvents. We will focus on the role of the van der Waals forces in determining the three-dimensional structures of these noncovalently bonded molecular systems and with the use of the high level ab initio DFT methodologies we will consider the effects of side-chains, end-chains, various chemical structural modifications along the chain backbones, different surrounding media (such as solvents), different supramolecular compositions on their structures and eventually properties such as energy levels, electronic band gaps and widths, conformational energies, absorption and emission spectra, charge transport and others. These computational studies are key to a greater understanding of how microscopic and nanoscale structures relate to macroscopic properties of these materials and will provide the scientific community and Canadian industry with information vital for the development of future more efficient devices made of organic semiconductors.

由有机共轭聚合物、低聚物和其他碳基分子系统制成的材料由于其在光电子学中的巨大潜力而目前是许多深入研究的主题。它们的应用已经在诸如太阳能电池、发光二极管、晶体管、集成电路、传感器、电致变色显示器、光开关、电光调制器、电池等器件中得到证实。已经发现，当这些器件具有多层和/或异质结构时，它们表现最佳。例如，本体异质结有机太阳能电池（其中富勒烯C60或C70与聚合物或低聚物共混）由于更平衡的电荷载流子传输而提供改进的性能。这些实验结果表明，弱分子间的货车德瓦尔斯（分散）力起着重要的作用，在确定（纳米级）的结构，因此，这些异质有机半导体的性能。理解有机半导体结构单元之间的复杂相互作用可以导致新材料的设计。这种理解和新材料的设计对于下一代有机光电应用的发展至关重要。使用计算方法，我的研究计划的长期目标是更好地了解异质纳米填充有机复合材料的主要成分如何相互作用，以及这些相互作用最终如何影响材料的整体电子和光学特性。我的团队将分子系统建模为孤立的链、超分子、纳米团簇或固体。我们的主要理论/计算工具是密度泛函理论（DFT）。我们计划使用各种类型的色散校正密度泛函理论来研究这些体系的分子结构。用含时密度泛函理论（TD-DFT）研究了聚合物的激发态，用固态密度泛函理论研究了聚合物的晶体结构。我们建议在溶液中以及在真空（气相）中研究这些系统。这是因为，即使溶剂通常在给定材料的制造的最后阶段被去除，也有许多实验指示（例如，聚集体形成）表明，在制造过程中使用的溶剂的类型影响器件的性能。我的研究的短期目标涉及的工业相关的（有前途的）有机多相纳米复合物的调查使用分散校正DFT和TD-DFT有和没有溶剂的存在下。我们将重点讨论货车力在确定这些非共价键合分子系统的三维结构中的作用，并使用高水平从头计算DFT方法，我们将考虑侧链，端链，沿着链骨架的各种化学结构修饰，不同的周围介质的影响（例如溶剂），不同的超分子组成对其结构和最终性质（例如能级、电子带隙和宽度、构象能、吸收和发射光谱、电荷传输等）的影响。这些计算研究是更好地理解微观和纳米级结构如何与这些材料的宏观性质相关的关键，并将为科学界和加拿大工业提供对开发未来更有效的有机半导体器件至关重要的信息。