Abstract
Cs4PbBr6 is a member of the halide perovskite family that is built from isolated (zero-dimensional) PbBr64- octahedra with Cs+ counter ions. The material exhibits anomalous optoelectronic properties: optical absorption and weak emission in the deep ultraviolet (310 - 375 nm) with efficient luminescence in the green region (540 nm). Several hypotheses have been proposed to explain the giant Stokes shift including: (i) CsPbBr3 phase impurities; (ii) self-trapped exciton; (iii) defect emission. We show -- within the modern first-principles theory of defects -- that many of the low energy point defects in Cs4PbBr6 lead to the formation of polybromide (Br3) species that exist in a range of charge states. We further demonstrate from excited-state calculations that tribromide moieties are photoresponsive and can contribute to the observed green luminescence. Photoactivity of polyhalide molecules is expected to be present in other halide perovskite-related compounds.
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