Picosecond Capture of Photoexcited Electrons Improves Photovoltaic Conversion in MAPbI3 :C70 -Doped Planar and Mesoporous Solar Cells

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - (2018) vom: 23. Aug., Seite e1801496
1. Verfasser: Gharibzadeh, Saba (VerfasserIn)
Weitere Verfasser: Valduga de Almeida Camargo, Franco, Roldán-Carmona, Cristina, Gschwend, Grégoire Clément, Pascual, Jorge, Tena-Zaera, Ramón, Cerullo, Giulio, Grancini, Giulia, Nazeeruddin, Mohammad Khaja
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article C70:MAPbI3 interface ETL free perovskite solar cells electron transfer hybrid perovskite solar cells ultrafast dynamics
Beschreibung
Zusammenfassung:© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
In this work, solar cells based on methylammonium lead iodide (MAPbI3 ) doped in solution with C70 fullerene in a mesoporous as well as planar electron-transporting layer (ETL)-free architecture are realized, showcasing in the latter case a record efficiency of 15.7% and an improved open-circuit voltage (VOC ). Contrary to the bulk heterojunction previously reported, the C70 molecules do not phase segregate and they are rather finely dispersed in the perovskite film, possibly infiltrating at the grain boundaries, while assisting the growth of a highly uniform perovskite layer. By means of time-resolved femtosecond-to-nanosecond optical spectroscopy, with an extended spectral coverage, it is observed that electrons photogenerated in the perovskite are transferred to C70 with a time constant of 20 ps. Despite being captured by C70 , electrons are not deeply trapped and can potentially bounce back into the perovskite, as suggested by the high fill factor and enhanced VOC of the MAPbI3 :C70 solar cells, especially in the case of the ETL-free device configuration
Beschreibung:Date Revised 27.02.2024
published: Print-Electronic
Citation Status Publisher
ISSN:1521-4095
DOI:10.1002/adma.201801496