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Efficient Ultraviolet Circularly Polarized Luminescence in Zero‐Dimensional Hybrid Cerium Bromides.

Authors :
Li, Chen
Wei, Yi
Zhang, Yan
Luo, Zhishan
Liu, Yulian
He, Meiying
Quan, Zewei
Source :
Angewandte Chemie International Edition. Jun2024, Vol. 63 Issue 26, p1-8. 8p.
Publication Year :
2024

Abstract

Ultraviolet circularly polarized luminescence (UV‐CPL) with high photon energy shows great potential in polarized light sources and stereoselective photopolymerization. However, developing luminescent materials with high UV‐CPL performance remains challenging. Here, we report a pair of rare earth Ce3+‐based zero‐dimensional (0D) chiral hybrid metal halides (HMHs), R/S‐(C14H24N2)2CeBr7, which exhibits characteristic UV emissions derived from the Ce 5d–4f transition. The compounds show simultaneously high photoluminescent quantum yields of (32–39)% and large luminescent dissymmetry factor (|glum|) values of (1.3–1.5)×10−2. Thus, the figures of merits of R/S‐(C14H24N2)2CeBr7 are calculated to be (4.5–5.8)×10−3, which are superior to the reported UV‐CPL emissive materials. Additionally, nearly 91 % of their PL intensities at 300 K can be well preserved at 380 K (LED operating temperature) without phase transition or decomposition, demonstrating the excellent structural and optical thermal stabilities of R/S‐(C14H24N2)2CeBr7. Based on these enantiomers, the fabricated UV‐emitting CP‐LEDs exhibit high polarization degrees of ±1.0 %. Notably, the UV‐CPL generated from the devices can significantly trigger the enantioselective photopolymerization of diacetylene with remarkable stereoselectivity, and consequently yield polymerized products with the anisotropy factors of circular dichroism (gCD) up to ±3.9×10−2, outperforming other UV‐CPL materials and demonstrating their great potential as UV‐polarized light sources. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14337851
Volume :
63
Issue :
26
Database :
Academic Search Index
Journal :
Angewandte Chemie International Edition
Publication Type :
Academic Journal
Accession number :
177903329
Full Text :
https://doi.org/10.1002/anie.202403727