@article{NikolisMischokSiegmundetal.2019,
  author    = {Nikolis, Vasileios C. and Mischok, Andreas and Siegmund, Bernhard and Kublitski, Jonas and Jia, Xiangkun and Benduhn, Johannes and H{\"o}rmann, Ulrich and Neher, Dieter and Gather, Malte C. and Spoltore, Donato and Vandewal, Koen},
  title     = {Strong light-matter coupling for reduced photon energy losses in organic photovoltaics},
  series = {Nature Communications},
  volume    = {10},
  journal   = {Nature Communications},
  publisher = {Nature Publ. Group},
  address   = {London},
  issn      = {2041-1723},
  doi       = {10.1038/s41467-019-11717-5},
  pages     = {8},
  year      = {2019},
  abstract  = {Strong light-matter coupling can re-arrange the exciton energies in organic semiconductors. Here, we exploit strong coupling by embedding a fullerene-free organic solar cell (OSC) photo-active layer into an optical microcavity, leading to the formation of polariton peaks and a red-shift of the optical gap. At the same time, the open-circuit voltage of the device remains unaffected. This leads to reduced photon energy losses for the low-energy polaritons and a steepening of the absorption edge. While strong coupling reduces the optical gap, the energy of the charge-transfer state is not affected for large driving force donor-acceptor systems. Interestingly, this implies that strong coupling can be exploited in OSCs to reduce the driving force for electron transfer, without chemical or microstructural modifications of the photoactive layer. Our work demonstrates that the processes determining voltage losses in OSCs can now be tuned, and reduced to unprecedented values, simply by manipulating the device architecture.},
  language  = {en}
}
@article{UllbrichBenduhnJiaetal.2019,
  author    = {Ullbrich, Sascha and Benduhn, Johannes and Jia, Xiangkun and Nikolis, Vasileios C. and Tvingstedt, Kristofer and Piersimoni, Fortunato and Roland, Steffen and Liu, Yuan and Wu, Jinhan and Fischer, Axel and Neher, Dieter and Reineke, Sebastian and Spoltore, Donato and Vandewal, Koen},
  title     = {Emissive and charge-generating donor-acceptor interfaces for organic optoelectronics with low voltage losses},
  series = {Nature materials},
  volume    = {18},
  journal   = {Nature materials},
  number    = {5},
  publisher = {Nature Publ. Group},
  address   = {London},
  issn      = {1476-1122},
  doi       = {10.1038/s41563-019-0324-5},
  pages     = {459 -- 464},
  year      = {2019},
  abstract  = {Intermolecular charge-transfer states at the interface between electron donating (D) and accepting (A) materials are crucial for the operation of organic solar cells but can also be exploited for organic light-emitting diodes(1,2). Non-radiative charge-transfer state decay is dominant in state-of-the-art D-A-based organic solar cells and is responsible for large voltage losses and relatively low power-conversion efficiencies as well as electroluminescence external quantum yields in the 0.01-0.0001\% range(3,4). In contrast, the electroluminescence external quantum yield reaches up to 16\% in D-A-based organic light-emitting diodes(5-7). Here, we show that proper control of charge-transfer state properties allows simultaneous occurrence of a high photovoltaic and emission quantum yield within a single, visible-light-emitting D-A system. This leads to ultralow-emission turn-on voltages as well as significantly reduced voltage losses upon solar illumination. These results unify the description of the electro-optical properties of charge-transfer states in organic optoelectronic devices and foster the use of organic D-A blends in energy conversion applications involving visible and ultraviolet photons(8-11).},
  language  = {en}
}