Rühle Sven, Dittrich Thomas
Department of Materials and Interfaces, Weizmann Institute of Science, Rehovot 76100, Israel.
J Phys Chem B. 2005 May 19;109(19):9522-6. doi: 10.1021/jp046211y.
We have investigated the electrostatic potential distribution in compact and nanoporous TiO2 films, deposited on conducting F-doped SnO2 substrate (FTO), which are used in dye-sensitized solar cells. The TiO2 films were immersed into aqueous electrolyte and excited from the FTO side by light pulses of a N2 laser while the current response was measured as a function of time. The measurements were carried out as a function of the pH value of the electrolyte and at different electrostatic potentials. For compact TiO2 films, the sign of the transient current at short response times changed when the applied electrostatic potential or the pH value was decreased. This was not observed for mesoporous TiO2 films directly deposited onto the FTO substrate without a compact TiO2 layer. We interpret the results in terms of a macroscopic electric field across the compact layer which is changed by the applied potential or the pH of the electrolyte. In contrast, measurements on mesoporous TiO2 films indicate that the contact region is mainly field-free, and we explain our results by a very sharp electrostatic potential drop within the first layer of particles at the TiO2/FTO interface.
我们研究了沉积在导电的氟掺杂二氧化锡衬底(FTO)上的致密和纳米多孔二氧化钛薄膜中的静电势分布,这些薄膜用于染料敏化太阳能电池。将二氧化钛薄膜浸入水性电解质中,并通过氮气激光的光脉冲从FTO一侧进行激发,同时测量电流响应随时间的变化。测量是作为电解质pH值的函数以及在不同静电势下进行的。对于致密的二氧化钛薄膜,当施加的静电势或pH值降低时,短响应时间下瞬态电流的符号会发生变化。对于直接沉积在没有致密二氧化钛层的FTO衬底上的介孔二氧化钛薄膜,未观察到这种情况。我们根据致密层上的宏观电场来解释结果,该电场会因施加的电势或电解质的pH值而改变。相比之下,对介孔二氧化钛薄膜的测量表明接触区域主要无电场,我们通过二氧化钛/FTO界面处第一层颗粒内非常陡峭的静电势降来解释我们的结果。