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Inverted non-fullerene organic solar cells: Charge carrier extraction and interface characterization

Subject Area Experimental Condensed Matter Physics
Electronic Semiconductors, Components and Circuits, Integrated Systems, Sensor Technology, Theoretical Electrical Engineering
Term from 2012 to 2022
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 196886395
 
Final Report Year 2022

Final Report Abstract

The aim of this research project was to gain a fundamental understanding of charge extraction via dedicated oxide interlayers in inverted organic solar cells (OSCs). To this end, in a close collaboration of the research teams at University of Wuppertal and TU Darmstadt we combined the study of the electro-optic device characteristics and photoelectron spectroscopy (PES) of the relevant organic/oxide interfaces. Our project was mainly focused on the electron extraction at the cathode (bottom) side of inverted OSCs. In the beginning of this project OSCs were almost exclusively based on fullerenes as acceptors, however we also considered non-fullerene acceptors in the last stage of our project. We initially studied the common phenomenon of light soaking in OSCs incorporating metal-oxide electron extraction layers (EEL), such as TiOx or ZnO. We were able to rule out a barrier at the interface ITO/TiOx and a potentially low bulk conductivity of TiOx as origin of the s-shaped J/V characteristics upon illumination without UV spectral components. Using a correlation of device data and photoelectron spectroscopy we were able to identify an extraction barrier between metal-oxide and fullerene. UV light soaking of the TiOx/organic acceptor interface reduced the barrier and improved electron extraction. We could also show that for the electrically doped Al:ZnO instead of TiOx no barrier is formed and UV light soaking is not required. As an alternative to electrical doping, we have identified plasmonic sensitization of metal-oxides by the introduction of metal-nanoparticles as an approach to mitigate the need for UV activation. Plasmonically mediated charge transfer from the metal nanoparticles to the metal-oxide already occurs upon illumination with hν

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