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Mechanical Characterization of Nanocomposite CdSe Quantum Dot – MEH-PPV Polymer Thin Films via Nanoindentation

机译:纳米压痕法对纳米复合CdSe量子点– MEH-PPV聚合物薄膜的力学表征

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摘要

Progress in the burgeoning field of organic electronics is enabling the development of novel technologies such as low-cost, printable solar cells and flexible, high-resolution displays. One exciting avenue of research in this field is nanostructured hybrid organics such as quantum dot (QD)-polymer devices. The incorporation of QDs can greatly improve a device’s efficiency and gives one the ability to tune its electrical and optical characteristics. In order for such technologies to be commercially viable, it is important to classify their mechanical integrity and reliability. Surprisingly little is known about the mechanical properties of QD-polymer thin films (u3c100 nm). This is in part due to challenges of: (1) isolating the mechanical response of a thin film from the underlying substrate, (2) obtaining a homogeneous dispersion of QDs in the film, and (3) the sensitivity of mechanical properties to the inherent rate dependence of polymer deformation (i.e., viscoelasticity). All of these challenges can introduce significant errors in the measurement of mechanical properties. Furthermore, the deformation mechanisms in nanocomposites are not well understood, so it is difficult to predict the effect of adding QDs on the mechanical behavior of films. In this thesis, these challenges are addressed for characterizing the mechanical properties of thin films of CdSe QD-poly[2-methoxy-5-2(2΄-ethylhexyloxy-p-phenylenevinylene)] (MEH-PPV) nanocomposites using quasi-static nanoindentation testing. Elastic modulus, hardness, and creep are measured as a function of QD concentration and loading and unloading rates. The QDsu27 ligands are removed by pyridine treatment prior to mixing with MEH-PPV to improve dispersion. The films are prepared via spin-coating onto glass substrates and subsequent annealing in air. Efforts are taken in the mechanical testing to minimize errors due to viscoelastic creep and interference from the substrate. Transmission electron microscopy reveals that the QDs are relatively well-dispersed in the polymer matrix. It is observed that adding QDs increases the elastic modulus (E) and hardness (H) of the films, while reducing the viscoelastic creep. Both E and H increase linearly with the volume percent of QDs. E ranges from 14.5 GPa to 52.7 GPa for pure MEH-PPV (0% QDs) and 100% QD films, respectively, while H ranges from 220 MPa to 1430 MPa for the same films, respectively. The films behave viscoelastically at lower QD loading, but assume a more granular character as the loading approaches 100%.
机译:在有机电子领域蓬勃发展中,进步使得诸如低成本,可打印太阳能电池和柔性,高分辨率显示器等新型技术得以发展。该领域中令人兴奋的研究途径是纳米结构的杂化有机物,例如量子点(QD)聚合​​物器件。集成QD可以大大提高设备的效率,并使设备能够调节其电气和光学特性。为了使这种技术在商业上可行,对它们的机械完整性和可靠性进行分类很重要。令人惊讶的是,对QD聚合物薄膜(<100 nm)的机械性能知之甚少。这部分是由于以下挑战:(1)将薄膜的机械响应与下面的基板隔离开来;(2)在薄膜中获得QD的均匀分散;以及(3)机械特性对固有特性的敏感性聚合物变形的速率依赖性(即粘弹性)。所有这些挑战都可能在机械性能的测量中引入重大错误。此外,对纳米复合材料的变形机理还没有很好的理解,因此很难预测添加QD对薄膜机械性能的影响。在本文中,这些挑战解决了使用准静态表征CdSe QD-聚[2-甲氧基-5-2(2′-乙基己氧基-对亚苯基亚乙烯基)](MEH-PPV)纳米复合材料薄膜的力学性能的问题。纳米压痕测试。弹性模量,硬度和蠕变是QD浓度和装卸速率的函数。在与MEH-PPV混合以改善分散之前,通过吡啶处理除去QDs27配体。通过旋涂到玻璃基板上并随后在空气中退火来制备薄膜。在机械测试中要尽力减少由于粘弹性蠕变和基材干扰引起的误差。透射电子显微镜显示,量子点在聚合物基质中相对分散。观察到添加QDs增加了膜的弹性模量(E)和硬度(H),同时减小了粘弹性蠕变。 E和H均随QD的体积百分比线性增加。对于纯MEH-PPV(0%QDs)和100%QD膜,E分别为14.5 GPa至52.7 GPa,而对于相同的膜,H分别为220 MPa至1430 MPa。薄膜在较低的QD载荷下表现出粘弹性,但当载荷接近100%时,呈现出更颗粒的特征。

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    McCumiskey Edward;

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  • 年度 2009
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