Abstract
Solution-processable perovskite nanocrystals (NCs) are gaining increasing interest in the field of photovoltaics because of their enhanced stability compared to their thin-film counterparts. However, the charge transfer dynamics in perovskite NC based light-harvesting systems are not well understood. By applying femtosecond differential transmission (DT) spectroscopy the photoinduced charge transfer from inorganic perovskite CsPbBr3 NCs to the fullerene derivative phenyl-C61-butyric acid methyl ester (PCBM) is investigated for two fundamentally different architectures, namely layer-by-layer heterostructures and blend structures. By varying the thickness of the NC layer on top of the PCBM in the layer-by-layer heterostructure, an exciton diffusion length of 290 +/- 28 nm for CsPbBr3 NC is extracted. The diffusion process is followed by an ultrafast exciton dissociation (within 200 fs) at the CsPbBr3 NC/PCBM interface. In blend structures an overall faster charge transfer process is observed. Furthermore, photoconductivity measurements on a blend structure-based photodetector reveal an effective charge extraction from the active layer resulting in a high photosensitivity. DT measurements on this blend structure including adjacent electron- or hole-transport layers give insight into the extraction process and suggest a certain degree of phase segregation, which assists the charge collection.
Dokumententyp: | Zeitschriftenartikel |
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Fakultät: | Physik |
Fakultätsübergreifende Einrichtungen: | Center for NanoScience (CENS) |
Themengebiete: | 500 Naturwissenschaften und Mathematik > 500 Naturwissenschaften
500 Naturwissenschaften und Mathematik > 530 Physik |
ISSN: | 2195-1071 |
Sprache: | Englisch |
Dokumenten ID: | 84183 |
Datum der Veröffentlichung auf Open Access LMU: | 15. Dez. 2021, 15:10 |
Letzte Änderungen: | 15. Dez. 2021, 15:10 |