期刊
ACS MATERIALS LETTERS
卷 1, 期 6, 页码 594-598出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsmaterialslett.9b00333
关键词
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资金
- Air Force Office of Scientific Research (AFOSR) [17RT0906]
- National Science Foundation [DMR-1709116, CHE-1664661, NSF-DMR-1606952]
- National Science Foundation under NSF [DMR-1644779]
- State of Florida
- U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division
Zero-dimensional (0D) organic metal halide hybrids are an emerging class of light emitting materials with exceptional photo-luminescence quantum efficiencies (PLQEs), thanks to their perfect host-guest structures with light emitting metal halide species periodically embedded in a wide band gap organic cationic matrix through ionic bonds. However, achieving efficient blue emissions is challenging for this class of materials, as structural distortions of metal halides often lead to large Stokes shifts. Here we report a highly luminescent blue emitting 0D organic lead bromide, (C13H19N4 )(2)PbBr4, with a peak emission of 460 nm (2.70 eV), a full width at half maximum (FWHM) of 66 nm (0.40 eV), a Stokes shift of 111 nm (0.85 eV), and a PLQE of similar to 40%. Single crystal structure analysis shows that individual PbBr42- species adopt a nearseesaw structure, which are coordinated to benzyl-hexamethylenetetrammonium (C13H19N4+) organic cations. The relatively small Stokes shift as compared to those of previously reported 0D organic metal halide hybrids are attributed to the low chemical reactivity of Pb 6s(2) lone pairs and the rigid organic cationic matrix. (C13H19N4)(2)PbBr4 also shows exceptional stability in air with little-to-no change of properties for more than a year in ambient conditions.
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