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Effect of macromolecular parameters and processing conditions on supramolecular organisation, morphology and electrical transport properties in thin layers of regioregular poly(3-hexylthiophene)

机译:大分子参数和加工条件对区域规则聚(3-己基噻吩)薄层中超分子组织,形态和电输运性质的影响

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The effects of molecular weight and the processing conditions on the polymer supramolecular organisation, its morphology and charge carriers mobility have been investigated for regioregular poly(3-hexylthiophene) (RR-P3HT) thin layers used for the fabrication of field-effect transistors (FETs). The application of three distinctly different processing techniques (dip coating, spin coating and drop casting) together with polymers exhibiting different molecular weights, including previously unexplored molecular weight value (120 kDa by SEC equal to 27 kDa after the MALDITOF correction) enabled the separation of the influence of purely macromolecular factors from the morphological ones. It has been demonstrated that the chain length of the deposited polymer is the determining factor in the fabrication of layers with high carriers mobility which changes from 10(-5) cm(2)/(V s) for the shortest chains (Mn corrected= 1 kDa) to 0.04 cm(2)/(V S) for the longest ones (Mn corrected = 27 kDa). The changes of the film morphology cannot explain the dependence of the mobility on Mn. The observed relationship can be rationalized by considering the principal factors, intervening on three different levels: (i) on the molecular level the increase of the conjugation length with Mn is observed which leads to a higher mobility of the carriers along a single chain; (ii) on the supramolecular level the probability of the interchain charge carriers hopping is higher for longer chains since the number of low activation energy pathways for the crossing between chains grows with the increase of the chain length; (iii) on the mesoscopic level the connectivity between aggregations of higher mobility, for example, nanorods observed by AFM, is better assured for longer polymer chains. The product of these contributions results in an enhanced carriers mobility for layers fabricated from high molecular weight polymer fractions. The morphology of the RR-P3HT layers is strongly dependent on the processing method used. For high rate deposition techniques (spin coating) nanorod-type morphologies are obtained for low molecular weight polymers whereas fractions of high molecular weight give films with a granular morphology. For low deposition rate techniques (dip coating) the rod-like morphology persists even for films fabricated from the highest molecular weight fraction. Moreover, for layers obtained from intermediate polymer fractions (from 1.9 to 10.8 kDa) the individual rod width is, within the experimental error, equal to the length of the polymer chain if the all trans conformation is assumed. The above obsenation implies that polymer chains are oriented perpendicularly to the rod long axis. GIXD investigations fully corroborate this hypothesis. The rod diameter in layers deposited using the highest molecular weight fraction (27 kDa) is significantly lower than the length of the chain in the all trans conformation, suggesting chain folds via all trans-all cis-all trans sequence of conformation changes which would limit the rod diameter. (c) 2006 Elsevier BX All rights reserved.
机译:分子量和加工条件对聚合物超分子组织,其形态和电荷载流子迁移率的影响已被研究用于制造场效应晶体管(FET)的区域规则聚(3-己基噻吩)(RR-P3HT)薄层)。三种截然不同的加工技术(浸涂,旋涂和滴铸)与表现出不同分子量的聚合物一起使用,包括先前未开发的分子量值(通过MALDITOF校正后,SEC的120 kDa等于27 kDa)使得能够分离出纯粹的大分子因素从形态因素的影响。已经证明,沉积的聚合物的链长是制造具有高载流子迁移率的层的决定因素,对于最短的链,载流子迁移率从10(-5)cm(2)/(V s)变化(Mn校正为= 1 kDa)到最长的0.04 cm(2)/(VS)(Mn校正= 27 kDa)。膜形态的变化不能解释迁移率对Mn的依赖性。可以通过考虑主要因素并在三个不同的水平上进行干预来使观察到的关系合理化:(i)在分子水平上,观察到与Mn的结合长度增加,这导致载体沿单链的迁移率更高; (ii)在超分子水平上,较长链的链间电荷载流子跳跃的可能性较高,因为链间交叉的低活化能途径的数目随链长的增加而增加; (iii)在介观水平上,对于更长的聚合物链,可以更好地确保较高迁移率的聚集体之间的连通性,例如通过原子力显微镜观察到的纳米棒。这些贡献的乘积导致由高分子量聚合物馏分制成的层的载流子迁移率提高。 RR-P3HT层的形态在很大程度上取决于所使用的处理方法。对于高速率沉积技术(旋涂),低分子量聚合物获得纳米棒型形貌,而高分子量级分则得到具有颗粒形貌的薄膜。对于低沉积速率技术(浸涂),即使对于由最高分子量分数制成的薄膜,棒状形态仍然存在。此外,对于由中间聚合物级分(1.9至10.8 kDa)获得的层,如果假定所有反式构象,则单个杆的宽度在实验误差范围内等于聚合物链的长度。上述感觉暗示聚合物链垂直于棒长轴取向。 GIXD调查充分证实了这一假设。使用最高分子量分数(27 kDa)沉积的层中的杆直径明显低于全反式构象的链长,这表明通过所有反式-顺式-反式构象变化的链折叠杆直径。 (c)2006 Elsevier BX保留所有权利。

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