@article{JordanFechlerXuetal.2015,
  author    = {Jordan, Thomas and Fechler, Nina and Xu, Jingsan and Brenner, Thomas J. K. and Antonietti, Markus and Shalom, Menny},
  title     = {"Caffeine Doping" of Carbon/Nitrogen-Based Organic Catalysts: Caffeine as a Supramolecular Edge Modifier for the Synthesis of Photoactive Carbon Nitride Tubes},
  series = {ChemCatChem : heterogeneous \& homogeneous \& bio- \& nano-catalysis ; a journal of ChemPubSoc Europe},
  volume    = {7},
  journal   = {ChemCatChem : heterogeneous \& homogeneous \& bio- \& nano-catalysis ; a journal of ChemPubSoc Europe},
  number    = {18},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {1867-3880},
  doi       = {10.1002/cctc.201500343},
  pages     = {2826 -- 2830},
  year      = {2015},
  abstract  = {An alternative method for the structure tuning of carbon nitride materials by using a supramolecular approach in combination with caffeine as lining-agent is described. The self-assembly of the precursor complex consisting of melamine and cyanuric acid can be controlled by this doping molecule in terms of morphology, electronic, and photophysical properties. Caffeine is proposed to insert as an edge-molecule eventually leading to hollow tube-like carbon nitride structures with improved efficiency of charge formation. Compared to the bulk carbon nitride, the caffeine-doped analogue possesses a higher photocatalytic activity for the degradation of rhodamineB dye. Furthermore, this approach is also shown to be suitable for the modification of carbon nitride electrodes.},
  language  = {en}
}
@article{LiebigSarhanPrietzeletal.2016,
  author    = {Liebig, Ferenc and Sarhan, Radwan Mohamed and Prietzel, Claudia Christina and Reinecke, Antje and Koetz, Joachim},
  title     = {"Green" gold nanotriangles: synthesis, purification by polyelectrolyte/micelle depletion flocculation and performance in surface-enhanced Raman scattering},
  series = {RSC Advances},
  volume    = {6},
  journal   = {RSC Advances},
  publisher = {Royal Society of Chemistry},
  address   = {Cambridge},
  issn      = {2046-2069},
  doi       = {10.1039/c6ra04808k},
  pages     = {33561 -- 33568},
  year      = {2016},
  abstract  = {The aim of this study was to develop a one-step synthesis of gold nanotriangles (NTs) in the presence of mixed phospholipid vesicles followed by a separation process to isolate purified NTs. Negatively charged vesicles containing AOT and phospholipids, in the absence and presence of additional reducing agents (polyampholytes, polyanions or low molecular weight compounds), were used as a template phase to form anisotropic gold nanoparticles. Upon addition of the gold chloride solution, the nucleation process is initiated and both types of particles, i.e., isotropic spherical and anisotropic gold nanotriangles, are formed simultaneously. As it was not possible to produce monodisperse nanotriangles with such a one-step procedure, the anisotropic nanoparticles needed to be separated from the spherical ones. Therefore, a new type of separation procedure using combined polyelectrolyte/micelle depletion flocculation was successfully applied. As a result of the different purification steps, a green colored aqueous dispersion was obtained containing highly purified, well-defined negatively charged flat nanocrystals with a platelet thickness of 10 nm and an edge length of about 175 nm. The NTs produce promising results in surface-enhanced Raman scattering.},
  language  = {en}
}
@article{MikelskisHorn2000,
  author    = {Mikelskis, Helmut and Horn, Martin Erik},
  title     = {"Holographie" als Thema im Physikunterricht},
  isbn      = {3-88064-294-X},
  year      = {2000},
  language  = {de}
}
@article{ChenSavateevPronkinetal.2017,
  author    = {Chen, Zupeng and Savateev, Aleksandr and Pronkin, Sergey and Papaefthimiou, Vasiliki and Wolff, Christian Michael and Willinger, Marc Georg and Willinger, Elena and Neher, Dieter and Antonietti, Markus and Dontsova, Dariya},
  title     = {"The Easier the Better" Preparation of Efficient Photocatalysts-Metastable Poly(heptazine imide) Salts},
  series = {Advanced materials},
  volume    = {29},
  journal   = {Advanced materials},
  publisher = {Wiley-VCH},
  address   = {Weinheim},
  issn      = {0935-9648},
  doi       = {10.1002/adma.201700555},
  pages     = {21800 -- 21806},
  year      = {2017},
  abstract  = {Cost-efficient, visible-light-driven hydrogen production from water is an attractive potential source of clean, sustainable fuel. Here, it is shown that thermal solid state reactions of traditional carbon nitride precursors (cyanamide, melamine) with NaCl, KCl, or CsCl are a cheap and straightforward way to prepare poly(heptazine imide) alkali metal salts, whose thermodynamic stability decreases upon the increase of the metal atom size. The chemical structure of the prepared salts is confirmed by the results of X-ray photoelectron and infrared spectroscopies, powder X-ray diffraction and electron microscopy studies, and, in the case of sodium poly(heptazine imide), additionally by atomic pair distribution function analysis and 2D powder X-ray diffraction pattern simulations. In contrast, reactions with LiCl yield thermodynamically stable poly(triazine imides). Owing to the metastability and high structural order, the obtained heptazine imide salts are found to be highly active photo-catalysts in Rhodamine B and 4-chlorophenol degradation, and Pt-assisted sacrificial water reduction reactions under visible light irradiation. The measured hydrogen evolution rates are up to four times higher than those provided by a benchmark photocatalyst, mesoporous graphitic carbon nitride. Moreover, the products are able to photocatalytically reduce water with considerable reaction rates, even when glycerol is used as a sacrificial hole scavenger.},
  language  = {en}
}
@article{HenkelGardinerNegretti2004,
  author    = {Henkel, Carsten and Gardiner, Simon A. and Negretti, Antonio},
  title     = {(De)coherence physics with condensates in microtraps},
  issn      = {1054-660X},
  year      = {2004},
  abstract  = {We discuss the dynamics of a condensate in a miniaturized electromagnetic trap formed above a microstructured substrate. Recent experiments have found that trap lifetimes get reduced when approaching the substrate because atoms couple to thermally excited near fields. The data agree quantitatively with our theory [Appl. Phys. B 69, 379 (1999)]. We focus on the decoherence of a quantum degenerate gas in a quasi-one-dimensional trap. Monte Carlo simulations indicate that atom interactions reduce the condensate decoherence rate. This is explained by a simple theory in terms of the suppression of long-wavelength excitations. We present preliminary simulation results for the adiabatic generation of dark solitons},
  language  = {en}
}
@article{PadeSchmidtStumpeetal.1996,
  author    = {Pade, Sylvia and Schmidt, Hartmut and Stumpe, Joachim and Fischer, Thomas M.},
  title     = {(Micro-)fluorescence spectroscopy of side chain polymers with bezanilide moieties},
  year      = {1996},
  language  = {en}
}
@article{Gardiner2002,
  author    = {Gardiner, Simon A.},
  title     = {(Quantum) chaos in Bose-Einstein condensates},
  issn      = {0950-0340},
  year      = {2002},
  language  = {de}
}
@article{MikatFrancoRegensteinetal.2000,
  author    = {Mikat, J{\"u}rgen E. R. and Franco, Olga and Regenstein, Wolfgang and Reck, G{\"u}nter and Knochenhauer, Gerald and Schulz, Burkhard and Orgzall, Ingo},
  title     = {1,3,4-oxadiazole crystals under high pressure-phase transitions and properties},
  year      = {2000},
  language  = {en}
}
@article{EichlerHaaseMenzel1995,
  author    = {Eichler, Hans Joachim and Haase, Alfred and Menzel, Ralf},
  title     = {100 watt average output power 1.2*diffraction limited beam from pulsed neodym single rod amplifier with SBS- phaseconjugation},
  year      = {1995},
  language  = {en}
}
@article{SchulzeBettBivouretal.2020,
  author    = {Schulze, Patricia S. C. and Bett, Alexander J. and Bivour, Martin and Caprioglio, Pietro and Gerspacher, Fabian M. and Kabakl{\i}, {\"O}zde Ş. and Richter, Armin and Stolterfoht, Martin and Zhang, Qinxin and Neher, Dieter and Hermle, Martin and Hillebrecht, Harald and Glunz, Stefan W. and Goldschmidt, Jan Christoph},
  title     = {25.1\% high-efficiency monolithic perovskite silicon tandem solar cell with a high bandgap perovskite absorber},
  series = {Solar RRL},
  volume    = {4},
  journal   = {Solar RRL},
  number    = {7},
  publisher = {John Wiley \& Sons, Inc.},
  address   = {New Jersey},
  pages     = {10},
  year      = {2020},
  abstract  = {Monolithic perovskite silicon tandem solar cells can overcome the theoretical efficiency limit of silicon solar cells. This requires an optimum bandgap, high quantum efficiency, and high stability of the perovskite. Herein, a silicon heterojunction bottom cell is combined with a perovskite top cell, with an optimum bandgap of 1.68 eV in planar p-i-n tandem configuration. A methylammonium-free FA(0.75)Cs(0.25)Pb(I0.8Br0.2)(3) perovskite with high Cs content is investigated for improved stability. A 10\% molarity increase to 1.1 m of the perovskite precursor solution results in approximate to 75 nm thicker absorber layers and 0.7 mA cm(-2) higher short-circuit current density. With the optimized absorber, tandem devices reach a high fill factor of 80\% and up to 25.1\% certified efficiency. The unencapsulated tandem device shows an efficiency improvement of 2.3\% (absolute) over 5 months, showing the robustness of the absorber against degradation. Moreover, a photoluminescence quantum yield analysis reveals that with adapted charge transport materials and surface passivation, along with improved antireflection measures, the high bandgap perovskite absorber has the potential for 30\% tandem efficiency in the near future.},
  language  = {en}
}