首页> 外文期刊>Bulletin of the Korean Chemical Society >Oxidation Behaviors of Poly(3-hexylthiophene-2,5-diyl) on Indium Tin Oxide Surfaces without and with Additional TiO2 Thin Films
【24h】

Oxidation Behaviors of Poly(3-hexylthiophene-2,5-diyl) on Indium Tin Oxide Surfaces without and with Additional TiO2 Thin Films

机译:聚(3-己基噻吩-2,5-二基)在有和没有其他TiO2薄膜的氧化铟锡表面上的氧化行为

获取原文
获取原文并翻译 | 示例
           

摘要

Poly(3-hexylthiophene-2,5-diyl) (P3HT) layers spin-coated on bare and TiO2-coated indium tin oxide (ITO) surfaces with two different TiO2 film thicknesses were exposed to visible light and humid atmosphere, and the oxidation behaviors these layers were studied using X-ray photoelectron spectroscopy. S atoms in P3HT were oxidized to sulfoxide without ring opening of P3HT under our experimental conditions. When the mean thickness of TiO2 on ITO was similar to 19 nm, oxidation of the S atoms on this substrate was more pronounced than on bare ITO and ITO covered with thinner TiO2 films (mean thickness: similar to 7 nm). Studies using photoluminescence (PL) suggest that electron-hole pairs created in P3HT on bare ITO can be transferred into the ITO and most likely recombine efficiently in ITO by electron-electron scattering. Relatively thin TiO2 films on ITO do not show much change in PL with respect to the case of bare ITO; however, when a thicker TiO2 film is deposited between ITO and P3HT, charge transfer from optically excited P3HT to ITO seems to be suppressed. Therefore, the probability for charge transfer from optically excited P3HT to O-2 and H2O, forming strong oxidizing agents such as O-2(-) and OH radicals, can be increased in the presence of a thicker TiO2 film on ITO.
机译:将旋涂在裸露的和TiO2涂层的氧化铟锡(ITO)表面上的聚(3-己基噻吩-2,5-二基)(P3HT)层暴露在可见光和潮湿的环境中,该氧化钛具有两种不同的TiO2膜厚度使用X射线光电子能谱研究了这些层的行为。在我们的实验条件下,P3HT中的S原子被氧化为亚砜而没有P3HT的开环。当ITO上TiO2的平均厚度接近19 nm时,与裸ITO和覆盖有更薄TiO2膜的ITO(平均厚度:近似7 nm)相比,该衬底上S原子的氧化更为明显。使用光致发光(PL)的研究表明,在裸ITO上的P3HT中创建的电子-空穴对可以转移到ITO中,并且很可能通过电子-电子散射在ITO中有效地重组。 ITO上相对较薄的TiO2膜相对于裸ITO而言,PL的变化不大。然而,当在ITO和P3HT之间沉积较厚的TiO2膜时,似乎抑制了从光激发的P3HT到ITO的电荷转移。因此,在ITO上存在较厚的TiO2膜时,可以增加电荷从光学激发的P3HT转移到O-2和H2O的可能性,形成强氧化剂,例如O-2(-)和OH自由基。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号