Polarizable Anionic Sublattices Can Screen Molecular Dipoles in Noncentrosymmetric Inorganic-Organic Hybrids

We report the growth and photophysical characterization of two polar hybrid lead halide phases, methylenedianiline lead iodide and bromide, (MDA)Pb2I6 and (MDA)Pb2Br6, respectively. The phases crystallize in noncentrosymmetric space group Fdd2, which produces a highly oriented molecular dipole moment that gives rise to second harmonic generation (SHG) upon excitation at 1064 nm. While both compositions are isostructural, the size dependence of the SHG signal suggests that the bromide exhibits a stronger phase-matching response whereas the iodide exhibits a significantly weaker non-phasematching signal. Similarly, fluorescence from (MDA)Pb2Br6 is observed around 630 nm below 75 K whereas only very weak luminescence from (MDA)Pb2I6 can be seen. We attribute the contrasting optical properties to differences in the character of the halide sublattice and postulate that the increased polarizability of the iodide ions acts to screen the local dipole moment, effectively reducing the local electric field in the crystals.

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We report the growth and photophysical characterization of two polar hybrid lead halide phases, methylenedianiline lead iodide and bromide, (MDA)Pb2I6 and (MDA)Pb2Br6, respectively. The noncentrosymmetric crystal structure of these phases leads to highly oriented molecular dipole moments, resulting in second harmonic generation (SHG) upon excitation at 1064 nm. The size dependence of the SHG signal indicates that the bromide exhibits a stronger phase-matching response while the iodide exhibits a significantly weaker non-phase-matching signal. Fluorescence from (MDA)Pb2Br6 is observed around 630 nm below 75 K, whereas (MDA)Pb2I6 exhibits very weak luminescence. The contrasting optical properties are attributed to differences in the character of the halide sublattice, with the increased polarizability of the iodide ions reducing the local electric field in the crystals.