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Reversible P3HT/Oxygen Charge Transfer Complex Identification in Thin Films Exposed to Direct Contact with Water

机译:可逆P3HT /氧气电荷转移复合膜在暴露于与水直接接触的薄膜中

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摘要

Combined systems of semiconducting polymers and aqueous electrolytes are emerging as a new frontier of organic electronics, with many promising applications in neuroscience, biomedicine, and photoelectrochemical cells. A detailed characterization of the effect of direct, prolonged contact with water in working conditions, typically upon visible light illumination, is thus urgently needed. Here, we report a comprehensive study of processes occurring in thin films of regioregular poly(3-hexylthiophene) (rr-P3HT), the election material for such applications, exposed to different environmental conditions. We demonstrate that the contact with saline solutions is not worse than contact with open air: in both situations the reversible formation of a charge transfer complex between polymer and molecular oxygen is the main phenomenon, enhanced by visible light illumination. Experimental data and theoretical modeling provide an insightful picture of the complex formation, as a precursor of photoactivated doping, and first unambiguously identify its spectral signature by means of vibrational spectroscopy techniques. In perspective, this work validates use of semiconducting polymers in contact with electrolytes and paves the way to new, rapidly emerging trends in organic electronics.
机译:半导体聚合物和含水电解质的组合体系是有机电子的新前沿,在神经科学,生物医学和光电化细胞中具有许多有前途的应用。因此,迫切需要在工作条件下直接延长与水的效果的详细表征,迫切需要在可见光照射时。在这里,我们报告了在植物聚(3-己基噻吩)(RR-P3HT)的薄膜中发生的过程的综合研究,这些应用的选配材料暴露于不​​同的环境条件。我们证明与盐水溶液的接触不比与露天的接触差是差的:在这种情况下,在聚合物和分子氧之间的电荷转移复合物的可逆形成是主要现象,通过可见光照明增强。实验数据和理论建模提供了一种复杂形成的富富态图片,作为光活化的掺杂的前体,并首先通过振动光谱技术揭示其光谱签名。在视角下,这项工作验证了使用半导体聚合物与电解质接触并铺平了有机电子产品的新的快速新兴趋势。

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