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Supramolecular hydrogen-bonded chiral networks enable blue circularly polarized emission from polymeric carbon quantum dotsopen access

Authors
Mal, SouravPark, YoungsinDas, DeblinaMeena, AbhisheekJo, YongcheolKyhm, KwangseukTaylor, Robert A.Jana, AtanuCho, Sangeun
Issue Date
2026
Publisher
Royal Society of Chemistry
Citation
Materials Horizons
Indexed
SCIE
SCOPUS
Journal Title
Materials Horizons
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/64055
DOI
10.1039/d6mh00085a
ISSN
2051-6347
2051-6355
Abstract
All-organic circularly polarized luminescence (CPL) emitters acting as intrinsic liquid polarizers provide a promising route to reduce optical crosstalk and enhance spatial resolution in displays by directly emitting circularly polarized light, thereby eliminating external polarizers and minimizing energy loss. Herein, we report a highly efficient, all-organic CPL-active liquid polarizer based on chiral organic binary composites (COBCs), in which camphorquinone-derived chiral inducers are integrated with polymeric carbon quantum dots (PCQDs), opening a previously unexplored pathway toward chiral organic-quantum dot composites. The composites exhibit intense blue emission with a photoluminescence quantum yield (PL QY) of 64%, and strong enantioselective CPL with luminescence dissymmetry factors (glum approximate to +/- 10-2). Circular dichroism spectroscopy reveals multiple Cotton effects with high absorption anisotropy (gabs = 1.2 & times; 10-2), while time-resolved photoluminescence and electrochemical analyses indicate that hydrogen-bonded chiral networks promote charge transfer and generate intrinsic chiral fields enabling selective CPL emission. A prototype device based on COBCs achieves a spatial resolution of 4 lp mm-1, nearly double that of achiral analogues, while effectively suppressing glare and enhancing image contrast. Our findings establish a design strategy for transforming achiral CQDs into CPL-active materials, opening pathways toward next-generation, energy-efficient photonic and display technologies.
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