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Organic metal halide hybrids with low-dimensional structures at the molecular level have received great attention recently for their exceptional structural tunability and unique photophysical properties. Here we report for the first time the synthesis and characterization of a one-dimensional (1D) organic metal halide hybrid, which contains metal halide nanoribbons with a width of three octahedral units. It is found that this material with a chemical formula C 8 H 28 N 5 Pb 3 Cl 11 shows a dual emission with a photoluminescence quantum efficiency (PLQE) of around 25%. Photophysical studies and density functional theory (DFT) calculations suggest the coexisting of delocalized free excitons and localized self-trapped excitons in metal halide nanoribbons leading to the dual emission.more » « lessFree, publicly-accessible full text available March 23, 2024
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The photophysical properties of square planar Pt(II) complexes are often strongly dependent on their self‐assembly modes and intermolecular Pt⋯Pt interactions. Controlling these interactions is important to achieve valuable properties for various applications, such as light‐emitting diodes and environmental sensing devices. Herein, a series of highly luminescent ionic Pt(II) complexes with tunable emission colors are reported, by controlling the molecular structures and interactions in solid state. Four ionic Pt(II) complexes, with a general formula [Pt(C^N)(N^N)]+X−(C^N = 2‐phenylpyridine or 2‐(2,4‐difluorophenyl)pyridine; N^N = 2,2′‐bipyridine; X−= chloride (Cl−) or tetraphenylborate (BPh4−), are designed, synthesized, and characterized. Due to the presence of intermolecular Pt⋯Pt interactions, strong metal–metal‐to‐ligand charge transfer (MMLCT) emissions are recorded in all four complexes with color changing from green to deep red in solid state. A high photoluminescence quantum efficiency (PLQE) of 81% is achieved for one of the complexes containing large BPh4−anions, due to the site isolation effects. Detailed structural and photophysical characterizations reveal a clear correlation between the stacking of these Pt(II) complexes and their photophysical properties, which can be well regulated by the molecular structures and counter‐anions.
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Abstract Zero‐dimensional (0D) organic metal halide hybrids (OMHHs) have recently emerged as a new class of light emitting materials with exceptional color tunability. While near‐unity photoluminescence quantum efficiencies (PLQEs) are routinely obtained for a large number of 0D OMHHs, it remains challenging to apply them as emitter for electrically driven light emitting diodes (LEDs), largely due to the low conductivity of wide bandgap organic cations. Here, the development of a new OMHH, triphenyl(9‐phenyl‐9H‐carbazol‐3‐yl) phosphonium antimony bromide (TPPcarzSbBr4), as emitter for efficient LEDs, which consists of semiconducting organic cations (TPPcarz+) and light emitting antimony bromide anions (Sb2Br82−), is reported. By replacing one of the phenyl groups in a well‐known tetraphenylphosphonium cation (TPP+) with an electroactive phenylcarbazole group, a semiconducting TPPcarz+cation is developed for the preparation of red emitting 0D TPPcarzSbBr4single crystals with a high PLQE of 93.8%. With solution processed TPPcarzSbBr4thin films (PLQE of 86.1%) as light emitting layer, red LEDs are fabricated to exhibit an external quantum efficiency (EQE) of 5.12%, a peak luminance of 5957 cd m−2, and a current efficiency of 14.2 cd A−1, which are the best values reported to date for electroluminescence devices based on 0D OMHHs.