4.8 Article

Revealing the nature of optical activity in carbon dots produced from different chiral precursor molecules

Journal

LIGHT-SCIENCE & APPLICATIONS
Volume 11, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41377-022-00778-9

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Funding

  1. Priority 2030 Federal Academic Leadership Program
  2. Research Grant Council of Hong Kong [CityU 11306619]
  3. Science Technology and Innovation Committee of Shenzhen Municipality [JCYJ20190808181201899]
  4. Russian Science Foundation [RSF21-73-10131]
  5. ITMO Fellowship and Professorship Program from the Government of the Russian Federation
  6. Ministry of Science and Higher Education of the Russian Federation through the Scholarship of the President of the Russian Federation for young scientists and graduate students [CPi-1807.2022.1, CPi-2180.2021.1]
  7. St. Petersburg State University [93021679]
  8. Russian Science Foundation [21-73-10131] Funding Source: Russian Science Foundation

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Carbon dots are promising nanoparticles for biology and medicine applications due to their easy fabrication, biocompatibility, and attractive optical properties. The researchers successfully synthesized chiral carbon dots using a one-step hydrothermal method, which exhibited high photoluminescence quantum yields, chiral optical signals, and stable optical characteristics. These chiral carbon dots have potential for various bio-applications.
Carbon dots (CDs) are light-emitting nanoparticles that show great promise for applications in biology and medicine due to the ease of fabrication, biocompatibility, and attractive optical properties. Optical chirality, on the other hand, is an intrinsic feature inherent in many objects in nature, and it can play an important role in the formation of artificial complexes based on CDs that are implemented for enantiomer recognition, site-specific bonding, etc. We employed a one-step hydrothermal synthesis to produce chiral CDs from the commonly used precursors citric acid and ethylenediamine together with a set of different chiral precursors, namely, L-isomers of cysteine, glutathione, phenylglycine, and tryptophan. The resulting CDs consisted of O,N-doped (and also S-doped, in some cases) carbonized cores with surfaces rich in amide and hydroxyl groups; they exhibited high photoluminescence quantum yields reaching 57%, chiral optical signals in the UV and visible spectral regions, and two-photon absorption. Chiral signals of CDs were rather complex and originated from a combination of the chiral precursors attached to the CD surface, hybridization of lower-energy levels of chiral chromophores formed within CDs, and intrinsic chirality of the CD cores. Using DFT analysis, we showed how incorporation of the chiral precursors at the optical centers induced a strong response in their circular dichroism spectra. The optical characteristics of these CDs, which can easily be dispersed in solvents of different polarities, remained stable during pH changes in the environment and after UV exposure for more than 400 min, which opens a wide range of bio-applications.

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