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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Dynamics of Interfacial Charge Transfer States and Carriers Separation in Dye-Sensitized Solar Cells: A Time-Resolved Terahertz Spectroscopy Study
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Dynamics of Interfacial Charge Transfer States and Carriers Separation in Dye-Sensitized Solar Cells: A Time-Resolved Terahertz Spectroscopy Study

机译:透析敏化太阳能电池中界面电荷转移状态和载体分离的动态:时间分辨的太赫兹光谱研究

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Electron injection from a photoexcited molecular sensitizer into a wide-bandgap semiconductor is the primary step toward charge separation in dye-sensitized solar cells (DSSCs). According to the current understanding of DSSCs functioning mechanism, charges are separated directly during this primary electron transfer process, yielding hot conduction band electrons in the semiconductor and positive holes localized on oxidized dye molecules at the surface. Comparing results of ultrafast transient absorption and time-resolved terahertz measurements, we show here that intermediate interfacial charge transfer states (CTSs) are rather formed upon ultrafast injection from photoexcited Ru(II)bipyridyl dye-sensitizer molecules into mesoporous TiO2 films. Formation and dissociation of these CTSs were found to strongly depend on their ionic environment and excess excitation energy. This finding establishes a new mechanism for charge separation in DSSCs. It also offers a rationale for the effect of electrolyte composition in liquid-based devices and of ion doping in solid-state solar cells under working conditions.
机译:从光屏蔽的分子敏化剂到宽带隙半导体中的电子注入是染料敏化太阳能电池(DSSCs)中的电荷分离的主要步骤。根据目前对DSSCS功能机构的理解,在该初级电子转移过程中直接分离电荷,在半导体中产生热导带电子,并且在表面的氧化染料分子上局部地定位的正孔。比较超快瞬态吸收和时间分辨的太赫兹测量的结果,我们在此显示中间界面电荷转移状态(CTS)在从光透镜Ru(II)双吡啶染料敏化剂分子中以超速注入到中孔TiO 2膜上。发现这些CTS的形成和解离强烈取决于其离子环境和过度的激发能量。此发现建立了一种新机制,用于DSSCS中的电荷分离。它还提供了在工作条件下固态太阳能电池中电解质组合物和离子掺杂的电解质组合物效果的理由。

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