@article{XuBrennerChenetal.2014,
  author    = {Xu, Jingsan and Brenner, Thomas J. K. and Chen, Zupeng and Neher, Dieter and Antonietti, Markus and Shalom, Menny},
  title     = {Upconversion-agent induced improvement of g-C3N4 photocatalyst under visible light},
  series = {ACS applied materials \& interfaces},
  volume    = {6},
  journal   = {ACS applied materials \& interfaces},
  number    = {19},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {1944-8244},
  doi       = {10.1021/am5051263},
  pages     = {16481 -- 16486},
  year      = {2014},
  abstract  = {Herein, we report the use of upconversion agents to modify graphite carbon nitride (g-C3N4) by direct thermal condensation of a mixture of ErCl3 center dot 6H(2)O and the supramolecular precursor cyanuric acid-melamine. We show the enhancement of g-C3N4 photoactivity after Er3+ doping by monitoring the photodegradation of Rhodamine B dye under visible light. The contribution of the upconversion agent is demonstrated by measurements using only a red laser. The Er3+ doping alters both the electronic and the chemical properties of g-C3N4. The Er3+ doping reduces emission intensity and lifetime, indicating the formation of new, nonradiative deactivation pathways, probably involving charge-transfer processes.},
  language  = {en}
}
@article{ProctorAlbrechtKuiketal.2014,
  author    = {Proctor, Christopher M. and Albrecht, Steve and Kuik, Martijn and Neher, Dieter and Thuc-Quyen Nguyen,},
  title     = {Overcoming geminate recombination and enhancing extraction in solution-processed small molecule solar cells},
  series = {dvanced energy materials},
  volume    = {4},
  journal   = {dvanced energy materials},
  number    = {10},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1614-6832},
  doi       = {10.1002/aenm.201400230},
  pages     = {7},
  year      = {2014},
  language  = {en}
}
@article{KraffertSteyrleuthnerAlbrechtetal.2014,
  author    = {Kraffert, Felix and Steyrleuthner, Robert and Albrecht, Steve and Neher, Dieter and Scharber, Markus C. and Bittl, Robert and Behrends, Jan},
  title     = {Charge Separation in PCPDTBT : PCBM Blends from an EPR Perspective},
  series = {The journal of physical chemistry},
  volume    = {118},
  journal   = {The journal of physical chemistry},
  number    = {49},
  publisher = {American Chemical Society},
  address   = {Washington},
  issn      = {1932-7447},
  doi       = {10.1021/jp509650v},
  pages     = {28482 -- 28493},
  year      = {2014},
  language  = {en}
}
@article{LiuTkachovKomberetal.2014,
  author    = {Liu, W. and Tkachov, R. and Komber, H. and Senkovskyy, V. and Schubert, M. and Wei, Z. and Facchetti, A. and Neher, Dieter and Kiriy, A.},
  title     = {Chain-growth polycondensation of perylene diimide-based copolymers: a new route to regio-regular perylene diimide-based acceptors for all-polymer solar cells and n-type transistors},
  series = {Polymer Chemistry},
  volume    = {5},
  journal   = {Polymer Chemistry},
  number    = {10},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {1759-9954},
  doi       = {10.1039/c3py01707a},
  pages     = {3404 -- 3411},
  year      = {2014},
  abstract  = {Herein, we report the chain-growth tin-free room temperature polymerization method to synthesize n-type perylene diimide-dithiophene-based conjugated polymers (PPDIT2s) suitable for solar cell and transistor applications. The palladium/electron-rich tri-tert-butylphosphine catalyst is effective to enable the chain-growth polymerization of anion-radical monomer Br-TPDIT-Br/Zn to PPDIT2 with a molecular weight up to M-w approximate to 50 kg mol(-1) and moderate polydispersity. This is the second example of the polymerization of unusual anion-radical aromatic complexes formed in a reaction of active Zn and electron-deficient diimide-based aryl halides. As such, the discovered polymerization method is not a specific reactivity feature of the naphthalene-diimide derivatives but is rather a general polymerization tool. This is an important finding, given the significantly higher maximum external quantum efficiency that can be reached with PDI-based copolymers (32-45\%) in all-polymer solar cells compared to NDI-based materials (15-30\%). Our studies revealed that PPDIT2 synthesized by the new method and the previously published polymer prepared by step-growth Stille polycondensation show similar electron mobility and all-polymer solar cell performance. At the same time, the polymerization reported herein has several technological advantages as it proceeds relatively fast at room temperature and does not involve toxic tin-based compounds. Because several chain-growth polymerization reactions are well-suited for the preparation of well-defined multi-functional polymer architectures, the next target is to explore the utility of the discovered polymerization in the synthesis of end-functionalized polymers and block copolymers. Such materials would be helpful to improve the nanoscale morphology of polymer blends in all-polymer solar cells.},
  language  = {en}
}