Chemical and Materials Science Center, National Renewable Energy Laboratory (NREL), Golden, Colorado 80401, United States.
ACS Nano. 2011 Oct 25;5(10):8267-74. doi: 10.1021/nn2029567. Epub 2011 Sep 20.
Sensitization of solid-state dye-sensitized solar cells (SSDSSCs) with a new, organic donor-π-acceptor dye with a large molar absorption coefficient led to an open-circuit voltage of over 1 V at AM1.5 solar irradiance (100 mW/cm(2)). Recombination of electrons in the TiO(2) film with the oxidized species in the hole-transfer material (HTM) was significantly slower with the organic dye than with a standard ruthenium complex dye. Density functional theory indicated that steric shielding of the electrons in the TiO(2) by the organic dye was important in reducing recombination. Preventing the loss of photoelectrons resulted in a significant voltage gain. There was no evidence that the organic dye contributed to the high voltage by shifting the band edges to more negative electrode potentials. Compared with an iodide-based liquid electrolyte, however, the more positive redox potential of the solid-state HTM used in the SSDSSCs favored higher voltages.
敏化具有大摩尔消光系数的新型有机给体-π-受体染料的固态染料敏化太阳能电池(SSDSSCs),在 AM1.5 阳光辐照(100 mW/cm(2))下开路电压超过 1 V。与标准钌配合物染料相比,TiO(2)薄膜中的电子与空穴传输材料(HTM)中氧化物种的复合要慢得多。密度泛函理论表明,TiO(2)中电子的空间位阻对减少复合很重要。防止光电子的损失导致了显著的电压增益。没有证据表明有机染料通过将能带边缘移向更负的电极电位来产生高电压。然而,与基于碘化物的液体电解质相比,SSDSSCs 中固态 HTM 的更正氧化还原电位有利于更高的电压。