Department of Chemical and Biomolecular Engineering, Sogang University, 1 Sinsu-dong, Mapo-gu, Seoul, Republic of Korea.
Phys Chem Chem Phys. 2013 Jul 14;15(26):10835-40. doi: 10.1039/c3cp50214g. Epub 2013 May 22.
Electron transport and recombination in three-dimensionally-ordered (3D-ordered) structure electrodes were investigated using intensity-modulated photocurrent and photovoltage spectroscopy. The surface-modified TiO2 inverse opal structure was applied as a 3D electrode. The morphology, crystalline structure and surface states of the 3D-ordered structure were characterized by SEM, TEM and XPS and compared to those of the conventional nanoparticulate TiO2 structure. The performance of the 3D electrode was also evaluated by comparing the transport time and recombination lifetime to those of the conventional electrodes. Remarkably, the recombination lifetime in inverse opal was found to be greater than in nanocrystalline TiO2 by 4.3-6.2 times, thus improving the electron collection efficiency by 10%. Comparing the photovoltaic performance, although the dye adsorption of the 3D-ordered porous electrode is lower, the electrode achieves a photocurrent density comparable to that of a nanoparticulate TiO2 electrode due to the higher light scattering as well as the higher collection efficiency.
使用强度调制光电流和光电压光谱法研究了三维有序结构电极中的电子输运和复合。采用表面修饰的 TiO2 反蛋白石结构作为 3D 电极。通过 SEM、TEM 和 XPS 对 3D 有序结构的形貌、晶体结构和表面状态进行了表征,并与传统的纳米颗粒 TiO2 结构进行了比较。还通过比较传输时间和复合寿命来评估 3D 电极的性能。值得注意的是,反蛋白石中的复合寿命比纳米晶 TiO2 长 4.3-6.2 倍,从而将电子收集效率提高了 10%。比较光伏性能,尽管 3D 有序多孔电极的染料吸附较低,但由于更高的光散射和更高的收集效率,电极实现了与纳米颗粒 TiO2 电极相当的光电流密度。