@phdthesis{PerdigonToro2022,
  author    = {Perdig{\´o}n-Toro, Lorena},
  title     = {On the Generation and Fate of Free Carriers in Non-Fullerene Acceptor Organic Solar Cells},
  doi       = {10.25932/publishup-55807},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-558072},
  school      = {Universit{\"a}t Potsdam},
  pages     = {ix, 191},
  year      = {2022},
  abstract  = {Organic solar cells offer an efficient and cost-effective alternative for solar energy harvesting. This type of photovoltaic cell typically consists of a blend of two organic semiconductors, an electron donating polymer and a low molecular weight electron acceptor to create what is known as a bulk heterojunction (BHJ) morphology. Traditionally, fullerene-based acceptors have been used for this purpose. In recent years, the development of new acceptor molecules, so-called non-fullerene acceptors (NFA), has breathed new life into organic solar cell research, enabling record efficiencies close to 19\%. Today, NFA-based solar cells are approaching their inorganic competitors in terms of photocurrent generation, but lag in terms of open circuit voltage (V_OC). Interestingly, the V_OC of these cells benefits from small offsets of orbital energies at the donor-NFA interface, although previous knowledge considered large energy offsets to be critical for efficient charge carrier generation. In addition, there are several other electronic and structural features that distinguish NFAs from fullerenes. My thesis focuses on understanding the interplay between the unique attributes of NFAs and the physical processes occurring in solar cells. By combining various experimental techniques with drift-diffusion simulations, the generation of free charge carriers as well as their recombination in state-of-the-art NFA-based solar cells is characterized. For this purpose, solar cells based on the donor polymer PM6 and the NFA Y6 have been investigated. The generation of free charge carriers in PM6:Y6 is efficient and independent of electric field and excitation energy. Temperature-dependent measurements show a very low activation energy for photocurrent generation (about 6 meV), indicating barrierless charge carrier separation. Theoretical modeling suggests that Y6 molecules have large quadrupole moments, leading to band bending at the donor-acceptor interface and thereby reducing the electrostatic Coulomb dissociation barrier. In this regard, this work identifies poor extraction of free charges in competition with nongeminate recombination as a dominant loss process in PM6:Y6 devices. Subsequently, the spectral characteristics of PM6:Y6 solar cells were investigated with respect to the dominant process of charge carrier recombination. It was found that the photon emission under open-circuit conditions can be almost entirely attributed to the occupation and recombination of Y6 singlet excitons. Nevertheless, the recombination pathway via the singlet state contributes only 1\% to the total recombination, which is dominated by the charge transfer state (CT-state) at the donor-acceptor interface. Further V_OC gains can therefore only be expected if the density and/or recombination rate of these CT-states can be significantly reduced. Finally, the role of energetic disorder in NFA solar cells is investigated by comparing Y6 with a structurally related derivative, named N4. Layer morphology studies combined with temperature-dependent charge transport experiments show significantly lower structural and energetic disorder in the case of the PM6:Y6 blend. For both PM6:Y6 and PM6:N4, disorder determines the maximum achievable V_OC, with PM6:Y6 benefiting from improved morphological order. Overall, the obtained findings point to avenues for the realization of NFA-based solar cells with even smaller V_OC losses. Further reduction of nongeminate recombination and energetic disorder should result in organic solar cells with efficiencies above 20\% in the future.},
  language  = {en}
}
@phdthesis{Hosseini2022,
  author    = {Hosseini, Seyed Mehrdad},
  title     = {Non-Langevin Recombination in Fullerene and Non-Fullerene Acceptor Solar Cells},
  doi       = {10.25932/publishup-54783},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-547831},
  school      = {Universit{\"a}t Potsdam},
  pages     = {XII, 103},
  year      = {2022},
  abstract  = {Organic solar cells (OSCs), in recent years, have shown high efficiencies through the development of novel non-fullerene acceptors (NFAs). Fullerene derivatives have been the centerpiece of the accepting materials used throughout organic photovoltaic (OPV) research. However, since 2015 novel NFAs have been a game-changer and have overtaken fullerenes. However, the current understanding of the properties of NFAs for OPV is still relatively limited and critical mechanisms defining the performance of OPVs are still topics of debate. In this thesis, attention is paid to understanding reduced-Langevin recombination with respect to the device physics properties of fullerene and non-fullerene systems. The work is comprised of four closely linked studies. The first is a detailed exploration of the fill factor (FF) expressed in terms of transport and recombination properties in a comparison of fullerene and non-fullerene acceptors. We investigated the key reason behind the reduced FF in the NFA (ITIC-based) devices which is faster non-geminate recombination relative to the fullerene (PCBM[70]-based) devices. This is then followed by a consideration of a newly synthesized NFA Y-series derivative which exhibits the highest power conversion efficiency for OSC at the time. Such that in the second study, we illustrated the role of disorder on the non-geminate recombination and charge extraction of thick NFA (Y6-based) devices. As a result, we enhanced the FF of thick PM6:Y6 by reducing the disorder which leads to suppressing the non-geminate recombination toward non-Langevin system. In the third work, we revealed the reason behind thickness independence of the short circuit current of PM6:Y6 devices, caused by the extraordinarily long diffusion length of Y6. The fourth study entails a broad comparison of a selection of fullerene and non-fullerene blends with respect to charge generation efficiency and recombination to unveil the importance of efficient charge generation for achieving reduced recombination. I employed transient measurements such as Time Delayed Collection Field (TDCF), Resistance dependent Photovoltage (RPV), and steady-state techniques such as Bias Assisted Charge Extraction (BACE), Temperature-Dependent Space Charge Limited Current (T-SCLC), Capacitance-Voltage (CV), and Photo-Induce Absorption (PIA), to analyze the OSCs. The outcomes in this thesis together draw a complex picture of multiple factors that affect reduced-Langevin recombination and thereby the FF and overall performance. This provides a suitable platform for identifying important parameters when designing new blend systems. As a result, we succeeded to improve the overall performance through enhancing the FF of thick NFA device by adjustment of the amount of the solvent additive in the active blend solution. It also highlights potentially critical gaps in the current experimental understanding of fundamental charge interaction and recombination dynamics.},
  language  = {en}
}