Chasing Charge Transfer States in DBP:C70 Organic solar Cells
Golnaz Sherafatipour  1, *@  , Koen Vandewal  2  , Morten Madsen  1@  
1 : NanoSYD, Mads Clausen Institute, University of Southern Denmark, Alsion 2, DK-6400 Sønderborg, Denmark
2 : Institute fur Angewandte Photophysik, Technische Universitst Dresden, Dresden, Germany
* : Corresponding author

Organic solar cells (OSC) are promising devices within the area of green energy technology, which can be fabricated from organic compounds with cheep techniques and on flexible or transparent substrates such as plastic or glass. OSCs are cost efficient, and lightweight devices that can exhibit high power conversion efficiencies (PCE) under low light irradiation. These advantages have made OSCs of great interest in research communities, where they have been extensively studied over the course of the past few years[1]. Despite these advantages, OSCs still exhibit low stability and lifetimes, which puts a barrier between laboratory achievements and industrial scale requirements. Therefore, in order to close this gap and obtain further improvements in device performance and long-term outdoor stability, a detailed understanding of the device degradation mechanism is required.

In an OSC, effective dissociation of the excitons takes place at the donor-acceptor interface via delocalized charge-transfer (CT) states, which represents intermediate states between the exciton dissociation and generation of free charges (or recombination back to the ground state). In this work, we investigate both electroluminescence (EL) created by bimolecular recombination via interface charge transfer states as well as sensitive external quantum efficiency measurements (sEQE) in DBP:C70 based OSCs, in order to study the role of CT states on degradation of the OSC devices[2]. The results from these measurements reveal valuable information about the loss mechanisms during OSC aging by considering the energetic and photo-physical behavior of the CT states, which also will set the base for further device modeling[3] and optimizing of the stability of the organic solar cells.

[1] Cao, H. et al. Recent progress in degradation and stabilization of organic solar cells. J. Power Sources 264, 168–183 (2014).

[2] Tvingstedt, K. et al. Electroluminescence from charge transfer states in polymer solar cells. J. Am. Chem. Soc. 131, 11819–11824 (2009).

[3] Liu, Y., Zojer, K., Lassen, B., Kjelstrup-hansen, J. & Madsen, M. The Role of Charge Transfer State on the Reduced Langevin Recombination in Organic Solar Cells : A Theoretical Study. J. Phys. Chem. C in press, (2015).



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