Hope, Michael AllanCordova, ManuelMishra, AdityaGunes, UmmugulsumCaiazzo, AlessandroDatta, KunalJanssen, Rene A. J.Emsley, Lyndon2024-03-182024-03-182024-03-182024-02-1910.1002/anie.202314856https://infoscience.epfl.ch/handle/20.500.14299/206447WOS:001165453500001Bandgap-tuneable mixed-halide 3D perovskites are of interest for multi-junction solar cells, but suffer from photoinduced spatial halide segregation. Mixed-halide 2D perovskites are more resistant to halide segregation and are promising coatings for 3D perovskite solar cells. The properties of mixed-halide compositions depend on the local halide distribution, which is challenging to study at the level of single octahedra. In particular, it has been suggested that there is a preference for occupation of the distinct axial and equatorial halide sites in mixed-halide 2D perovskites. Pb-207 NMR can be used to probe the atomic-scale structure of lead-halide materials, but although the isotropic Pb-207 shift is sensitive to halide stoichiometry, it cannot distinguish configurational isomers. Here, we use 2D isotropic-anisotropic correlation 207Pb NMR and relativistic DFT calculations to distinguish the [PbX6] configurations in mixed iodide-bromide 3D FAPb(Br1-xIx)(3) perovskites and 2D BA(2)Pb(Br1-xIx)(4) perovskites based on formamidinium (FA(+)) and butylammonium (BA(+)), respectively. We find that iodide preferentially occupies the axial site in BA-based 2D perovskites, which may explain the suppressed halide mobility.Physical SciencesAb Initio Calculations2D Halide PerovskitesHalide SegregationNmr SpectroscopyPhotovoltaic Materialstext::journal::journal article::research article