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Tuning Fullerene Intercalation in a Poly (thiophene) derivative by Controlling the Polymer Degree of Self-Organisation

机译:通过控制聚合物的自组织度来调节聚噻吩衍生物中的富勒烯插层

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摘要

Controlling the nanoscale arrangement in polymer-fullerene organic solar cells is of paramount importance to boost the performance of such promising class of photovoltaic diodes. In this work, we use a pseudo-bilayer system made of poly(2,5-bis(3-hexadecylthiophen-2-yl)thieno[3,2-b]thiophene (PBTTT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM), to acquire a more complete understanding of the diffusion and intercalation of the fullerene-derivative within the polymer layer. By exploiting morphological and structural characterisation techniques, we observe that if we increase the film solidification time the polymer develops a higher crystalline order, and, as a result, it does not allow fullerene molecules to intercalate between the polymer side-chains. Gaining insight into the detailed fullerene intercalation mechanism is important for the development of organic photovoltaic diodes (PVDs).
机译:控制聚合物-富勒烯有机太阳能电池中的纳米级排列对于提高此类有前途的光电二极管的性能至关重要。在这项工作中,我们使用由聚(2,5-双(3-十六烷基噻吩-2-基)噻吩并[3,2-b]噻吩(PBTTT)和[6,6]-苯基- C61-丁酸甲酯(PCBM),以更全面地了解富勒烯衍生物在聚合物层中的扩散和嵌入,通过利用形态学和结构表征技术,我们观察到,如果增加膜的固化时间,聚合物形成更高的结晶顺序,因此不允许富勒烯分子插入聚合物侧链之间,深入了解富勒烯的详细嵌入机制对于有机光电二极管(PVD)的开发非常重要。

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