Voïtchovsky Kislon, Ashari-Astani Negar, Tavernelli Ivano, Tétreault Nicolas, Rothlisberger Ursula, Stellacci Francesco, Grätzel Michael, Harms Hauke A
†EPFL STI IMX SUNMIL, Station 12, CH-1015 Lausanne, Switzerland.
‡Physics Department, Durham University, Durham DH1 3LE, United Kingdom.
ACS Appl Mater Interfaces. 2015 May 27;7(20):10834-42. doi: 10.1021/acsami.5b01638. Epub 2015 May 15.
Amphiphilic sensitizers are central to the function of dye-sensitized solar cells. It is known that the cell's performance depends on the molecular arrangement and the density of the dye on the semiconductor surface, but a molecular-level picture of the cell-electrolyte interface is still lacking. Here, we present subnanometer in situ atomic force microscopy images of the Z907 dye at the surface of TiO2 in a relevant liquid. Our results reveal changes in the conformation and the lateral arrangement of the dye molecules, depending on their average packing density on the surface. Complementary quantitative measurements on the ensemble of the film are obtained by the quartz-crystal microbalance with dissipation technique. An atomistic picture of the dye coverage-dependent packing, the effectiveness of the hydrophobic alkyl chains as blocking layer, and the solvent accessibility is obtained from molecular dynamics simulations.
两亲性敏化剂是染料敏化太阳能电池功能的核心。已知电池性能取决于染料在半导体表面的分子排列和密度,但仍缺乏电池 - 电解质界面的分子水平图像。在此,我们展示了在相关液体中TiO₂表面Z907染料的亚纳米原位原子力显微镜图像。我们的结果揭示了染料分子的构象和横向排列的变化,这取决于它们在表面的平均堆积密度。通过具有耗散技术的石英晶体微天平对薄膜整体进行了补充定量测量。从分子动力学模拟中获得了染料覆盖度依赖性堆积、疏水烷基链作为阻挡层的有效性以及溶剂可及性的原子级图像。