钙钛矿(结构)
卤化物
材料科学
介孔材料
钙钛矿太阳能电池
光电子学
沉积(地质)
色素敏化染料
太阳能电池
载流子
纳米技术
化学工程
化学
无机化学
电极
古生物学
生物化学
物理化学
沉积物
工程类
电解质
生物
催化作用
作者
Tomas Leijtens,Beat Lauber,Giles E. Eperon,Samuel D. Stranks,Henry J. Snaith
摘要
Emerging from the field of dye-sensitized solar cells, organometal halide perovskite-based solar cells have recently attracted considerable attention. In these devices, the perovskite light absorbers can also be used as charge transporting materials, changing the requirements for efficient device architectures. The perovskite deposition can vary from merely sensitizing the TiO2 electron transporting scaffold as an endowment of small nanoparticles, to completely filling the pores where it acts as both light absorber and hole transporting material in one. By decreasing the TiO2 scaffold layer thickness, we change the solar cell architecture from perovskite-sensitized to completely perovskite-filled. We find that the latter case leads to improvements in device performance because higher electron densities can be sustained in the TiO2, improving electron transport rates and photovoltage. Importantly, the primary recombination pathway between the TiO2 and the hole transporting material is blocked by the perovskite itself. This understanding helps to rationalize the high voltages attainable on mesoporous TiO2-based perovskite solar cells.
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