光致发光
钙钛矿(结构)
电子转移
纳秒
材料科学
电子
分析化学(期刊)
通量
动力学
化学
光电子学
结晶学
光学
光化学
物理
离子
激光器
有机化学
量子力学
色谱法
作者
Xiangtian Chen,Hannu P. Pasanen,Ramsha Khan,Nikolai V. Tkachenko,Csaba Janáky,Gergely F. Samu
标识
DOI:10.1021/acs.jpclett.3c03536
摘要
The kinetics of electron extraction at the electron transfer layer/perovskite interface strongly affects the efficiency of a perovskite solar cell. By combining transient absorption and time-resolved photoluminescence spectroscopy, the electron extraction process between FA0.83Cs0.17Pb(I0.83Br0.17)3 and TiO2 single crystals with different orientations of (100), (110), and (111) were probed from subpicosecond to several hundred nanoseconds. It was revealed that the band alignment between the constituents influenced the relative electron extraction process. TiO2(100) showed the fastest overall and hot electron transfer, owing to the largest conduction band and Fermi level offset compared to FA0.83Cs0.17Pb(I0.83Br0.17)3. It was found that an early electron accumulation in these systems can have an influence on the following electron extraction on the several nanosecond time scale. Furthermore, the existence of a potential barrier at the TiO2/perovskite interface was also revealed by performing excitation fluence-dependent measurements.
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