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Single crystalline bulk assemblies of metal halide clusters show great potential as highly efficient light emitters with tunable photophysical properties. However, synthetic control of the geometry of the clusters in a rational manner has not been well established, and the relationships between the photophysical properties and structures of this emerging class of zero-dimensional materials are still not well understood. Here, we report the synthesis and characterization of two bulk assemblies of lead bromide clusters, (bmpy) 6 [Pb 3 Br 12 ] ( T1 ) and (bmpy) 9 [ZnBr 4 ] 2 [Pb 3 Br 11 ] ( T2 ) (bmpy: 1-butyl-1-methylpyrrolidinium), which contain metal halide trimer clusters with different geometries. T1 with chain-shaped [Pb 3 Br 12 ] 6– clusters is not emissive at room temperature, whereas T2 with triangle-shaped [Pb 3 Br 11 ] 5– clusters exhibits yellowish-green emission peaked at 564 nm with a photoluminescence quantum efficiency of 7% at room temperature. Detailed analysis of the structural and photophysical properties show that the photophysical properties and excited-state dynamics of these materials are highly dependent on the geometry of the metal halide clusters.
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Lee et al. (2019) studied this question.
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