Abstract
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[Pb3Br12] (T1) and (bmpy)9[ZnBr4]2[Pb3Br11] (T2) (bmpy: 1-butyl-1-methylpyrrolidinium), which contain metal halide trimer clusters with different geometries. T1 with chain-shaped [Pb3Br12]6- clusters is not emissive at room temperature, whereas T2 with triangle-shaped [Pb3Br11]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.
Original language | English |
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Pages (from-to) | 374-380 |
Number of pages | 7 |
Journal | Chemistry of Materials |
Volume | 32 |
Issue number | 1 |
DOIs | |
State | Published - Jan 14 2020 |
Externally published | Yes |
Funding
This work is supported by the National Science Foundation (DMR-1709116) and the Air Force Office of Scientific Research (AFOSR) (17RT0906). J.N. acknowledges support from NSF-DMR-1606952. Part of the work was carried out at the National High Magnetic Field Laboratory, which is supported by the National Science Foundation under NSF DMR-1644779 and the State of Florida. The authors thank Dr. Kenneth Hanson for the help with emission measurements.