@article{FranzToebbensSteckhanetal.2018,
  author    = {Franz, Alexandra and T{\"o}bbens, Daniel M. and Steckhan, Julia and Schorr, Susan},
  title     = {Determination of the miscibility gap in the solid solutions series of methylammonium lead iodide/chloride},
  series = {Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials},
  volume    = {74},
  journal   = {Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials},
  publisher = {International Union of Crystallography},
  address   = {Chester},
  issn      = {2052-5206},
  doi       = {10.1107/S2052520618010764},
  pages     = {445 -- 449},
  year      = {2018},
  abstract  = {Perovskites are widely known for their enormous possibility of elemental substitution, which leads to a large variety of physical properties. Hybrid perovskites such as CH3NH3PbI3 (MAPbI(3)) and CH3NH3PbCl3 (MAPbCl(3)) are perovskites with an A([XII])B([VI)X(-)([II)(])structure, where A is an organic molecule, B is a lead(II) cation and X is a halide anion of iodine or chlorine. Whereas MAPbCl(3) crystallizes in the cubic space group Pm (3) over barm, MAPbI(3) is in the tetragonal space group I4/mcm. The substitution of I by Cl leads to an increased tolerance against humidity but is challenging or even impossible due to their large difference in ionic radii. Here, the influence of an increasing Cl content in the reaction solution on the miscibility of the solid solution members is examined systematically. Powders were synthesized by two different routes depending on the I:Cl ratio. High-resolution synchrotron X-ray data are used to establish values for the limits of the miscibility gap which are 3.1 (1.1) mol\% MAPbCl(3) in MAPI(3) and 1.0 (1) mol\% MAPbI(3) in MAPCl. The establishment of relations between average pseudo-cubic lattice parameters for both phases allows a determination of the degree of substitution from the observed lattice parameters.},
  language  = {en}
}
@article{FranzToebbensLehmannetal.2020,
  author    = {Franz, Alexandra and T{\"o}bbens, Daniel M. and Lehmann, Frederike and K{\"a}rgell, Martin and Schorr, Susan},
  title     = {The influence of deuteration on the crystal structure of hybrid halide perovskites: a temperature-dependent neutron diffraction study of FAPbBr(3)},
  series = {Acta crystallographica; Section B, Structural science, crystal engineering and materials},
  volume    = {76},
  journal   = {Acta crystallographica; Section B, Structural science, crystal engineering and materials},
  number    = {2},
  publisher = {Wiley-Blackwell},
  address   = {Oxford [u.a.]},
  issn      = {2052-5206},
  doi       = {10.1107/S2052520620002620},
  pages     = {267 -- 274},
  year      = {2020},
  abstract  = {This paper discusses the full structural solution of the hybrid perovskite formamidinium lead tribromide (FAPbBr(3)) and its temperature-dependent phase transitions in the range from 3 K to 300 K using neutron powder diffraction and synchrotron X-ray diffraction. Special emphasis is put on the influence of deuteration on formamidinium, its position in the unit cell and disordering in comparison to fully hydrogenated FAPbBr(3). The temperature-dependent measurements show that deuteration critically influences the crystal structures, i.e. results in partially-ordered temperature-dependent structural modifications in which two symmetry-independent molecule positions with additional dislocation of the molecular centre atom and molecular angle inclinations are present.},
  language  = {en}
}