@article{GorenflotPaulkePiersimonietal.2018,
  author    = {Gorenflot, Julien and Paulke, Andreas and Piersimoni, Fortunato and Wolf, Jannic and Kan, Zhipeng and Cruciani, Federico and El Labban, Abdulrahman and Neher, Dieter and Beaujuge, Pierre M. and Laquai, Frederic},
  title     = {From recombination dynamics to device performance},
  series = {dvanced energy materials},
  volume    = {8},
  journal   = {dvanced energy materials},
  number    = {4},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1614-6832},
  doi       = {10.1002/aenm.201701678},
  pages     = {12},
  year      = {2018},
  abstract  = {An original set of experimental and modeling tools is used to quantify the yield of each of the physical processes leading to photocurrent generation in organic bulk heterojunction solar cells, enabling evaluation of materials and processing condition beyond the trivial comparison of device performances. Transient absorption spectroscopy, "the" technique to monitor all intermediate states over the entire relevant timescale, is combined with time-delayed collection field experiments, transfer matrix simulations, spectral deconvolution, and parametrization of the charge carrier recombination by a two-pool model, allowing quantification of densities of excitons and charges and extrapolation of their kinetics to device-relevant conditions. Photon absorption, charge transfer, charge separation, and charge extraction are all quantified for two recently developed wide-bandgap donor polymers: poly(4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b′]dithiophene-3,4-difluorothiophene) (PBDT[2F]T) and its nonfluorinated counterpart poly(4,8-bis((2-ethylhexyl)oxy)benzo[1,2-b:4,5-b′]dithiophene-3,4-thiophene) (PBDT[2H]T) combined with PC71BM in bulk heterojunctions. The product of these yields is shown to agree well with the devices' external quantum efficiency. This methodology elucidates in the specific case studied here the origin of improved photocurrents obtained when using PBDT[2F]T instead of PBDT[2H]T as well as upon using solvent additives. Furthermore, a higher charge transfer (CT)-state energy is shown to lead to significantly lower energy losses (resulting in higher VOC) during charge generation compared to P3HT:PCBM.},
  language  = {en}
}
@article{LoveFeuersteinWolffetal.2017,
  author    = {Love, John A. and Feuerstein, Markus and Wolff, Christian Michael and Facchetti, Antonio and Neher, Dieter},
  title     = {Lead Halide Perovskites as Charge Generation Layers for Electron Mobility Measurement in Organic Semiconductors},
  series = {ACS applied materials \& interfaces},
  volume    = {9},
  journal   = {ACS applied materials \& interfaces},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {1944-8244},
  doi       = {10.1021/acsami.7b10361},
  pages     = {42011 -- 42019},
  year      = {2017},
  abstract  = {Hybrid lead halide perovskites are introduced as charge generation layers (CGLs) for the accurate determination of electron mobilities in thin organic semiconductors. Such hybrid perovskites have become a widely studied photovoltaic material in their own right, for their high efficiencies, ease of processing from solution, strong absorption, and efficient photogeneration of charge. Time-of-flight (ToF) measurements on bilayer samples consisting of the perovskite CGL and an organic semiconductor layer of different thickness are shown to be determined by the carrier motion through the organic material, consistent with the much higher charge carrier mobility in the perovskite. Together with the efficient photon-to-electron conversion in the perovskite, this high mobility imbalance enables electron-only mobility measurement on relatively thin application-relevant organic films, which would not be possible with traditional ToF measurements. This architecture enables electron-selective mobility measurements in single components as well as bulk-heterojunction films as demonstrated in the prototypical polymer/fullerene blends. To further demonstrate the potential of this approach, electron mobilities were measured as a function of electric field and temperature in an only 127 nm thick layer of a prototypical electron-transporting perylene diimide-based polymer, and found to be consistent with an exponential trap distribution of ca. 60 meV. Our study furthermore highlights the importance of high mobility charge transporting layers when designing perovskite solar cells.},
  language  = {en}
}
@misc{CardinalettiKestersBerthoetal.2014,
  author    = {Cardinaletti, Ilaria and Kesters, Jurgen and Bertho, Sabine and Conings, Bert and Piersimoni, Fortunato and Lutsen, Laurence and Nesladek, Milos and Van Mele, Bruno and Van Assche, Guy and Vandewal, Koen and Salleo, Alberto and Vanderzande, Dirk and Maes, Wouter and Manca, Jean V.},
  title     = {Toward bulk heterojunction polymer solar cells with thermally stable active layer morphology},
  series = {Journal of photonics for energy},
  volume    = {4},
  journal   = {Journal of photonics for energy},
  publisher = {SPIE},
  address   = {Bellingham},
  issn      = {1947-7988},
  doi       = {10.1117/1.JPE.4.040997},
  pages     = {12},
  year      = {2014},
  abstract  = {When state-of-the-art bulk heterojunction organic solar cells with ideal morphology are exposed to prolonged storage or operation at elevated temperatures, a thermally induced disruption of the active layer blend can occur, in the form of a separation of donor and acceptor domains, leading to diminished photovoltaic performance. Toward the long-term use of organic solar cells in real-life conditions, an important challenge is, therefore, the development of devices with a thermally stable active layer morphology. Several routes are being explored, ranging from the use of high glass transition temperature, cross-linkable and/or side-chain functionalized donor and acceptor materials, to light-induced dimerization of the fullerene acceptor. A better fundamental understanding of the nature and underlying mechanisms of the phase separation and stabilization effects has been obtained through a variety of analytical, thermal analysis, and electro-optical techniques. Accelerated aging systems have been used to study the degradation kinetics of bulk heterojunction solar cells in situ at various temperatures to obtain aging models predicting solar cell lifetime. The following contribution gives an overview of the current insights regarding the intrinsic thermally induced aging effects and the proposed solutions, illustrated by examples of our own research groups. (C) The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License.},
  language  = {en}
}