光电诱导形成多噻吩/TiO2纳米杂化异质结薄膜在太阳能电池中的应用

Y. Otsuka, Y. Okamoto, H. Y. Akiyama, K. Umekita, Y. Tachibana, S. Kuwabata
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引用次数: 34

摘要

研究了在TiO2纳米孔内光诱导聚合噻吩形成纳米结构的聚噻吩/TiO2异质结薄膜。所得薄膜在TiO2纳米孔域内具有纳米杂化和电子连接。光聚合过程分为三个阶段:(i)光激发共价附着在TiO2表面的噻吩,(ii)附着在TiO2表面的噻吩的电子注入反应,以及(iii)电解质中的噻吩反应物的电子转移到附着在表面的噻吩上。最初的快速光聚合和随后的缓慢聚合物生长是通过一系列实验的分析来解释的,例如,光照射时间、应用偏压、电解质类型、噻吩反应物类型和它们的形态。对吸附在TiO2上的噻吩进行电化学测量,发现其氧化还原电位分布广泛。这可以解释为TiO2表面局部电场的影响以及表面结合的噻吩与TiO2之间的强相互作用。将纳米杂化膜应用于感光型光电化学太阳能电池,证实了纳米杂化膜在电子器件上的直接应用。太阳能电池的性能与纳米杂化膜的界面结构和光聚合度密切相关。
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Photoinduced Formation of Polythiophene/TiO2 Nanohybrid Heterojunction Films for Solar Cell Applications
Formation of nanostructured polythiophene/TiO2 heterojunction films, using photoinduced polymerization of thiophene inside TiO2 nanopores, was investigated. The resultant film possesses nanohybridization and electronic connection within the TiO2 nanoporous domain. Photopolymerization proceeded in three stages: (i) photoexcitation of bithiophene covalently attached to the TiO2 surface, (ii) an electron injection reaction from the surface attached thiophene to the TiO2, and (iii) an electron transfer from a thiophene reactant in an electrolyte to the surface-attached bithiophene. Initial rapid photopolymerization and subsequent slow polymer growth were explained by analysis of a series of experiments, e.g., with respect to light irradiation time, applied bias, electrolyte types, thiophene reactant type, and their morphology. Electrochemical measurements for the bithiophene adsorbed on TiO2 revealed a wide distribution of redox potentials. This was explained by influence of the local electric field on the TiO2 surface in addition to strong interaction between the surfacebound bithiophene and the TiO2. The nanohybrid film was applied to a sensitized-type photoelectrochemical solar cell, substantiating direct application of the nanohybrid film to electronic devices. The solar cell performance was closely associated with the interfacial structure in the nanohybrid film and the photopolymerization degree.
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