Post‐Synthetic Graphitization and Photoluminescence Tuning of Carbon Dots from <i>L</i>‐Glutamic Acid

Carbon dots are promising luminescent nanostructures. Their availability, based on inexpensive precursors and their intrinsic fluorescent nature, place them as potential choices against traditional quantum dots in some applications. However, the carbon dots nature is nowadays not well defined and understood. They are usually hybrid nanomaterials in terms of structure and composition, which hinders the knowledge of their photoluminescence mechanisms. Herein, the solvent‐free pyrolysis of L ‐glutamic acid by microwave synthesis leads to an incomplete graphitization of the precursor resulting in loose polymer‐like nanohybrids. Further experiments confirm that these carbon dots (CD) can be crosslinked and graphitized in a second heating step when using temperatures above 160 °C, reaching a plateau of graphitization over 200 °C. An exhaustive analysis by thermogravimetric analysis, Raman and X‐ray photoelectron spectroscopy highlights the structural changes undergo from 140 to 200 °C, where an increase of stability is observed due to the graphitization process. The condensation and decarboxylation reactions with loss of hydrophilic functional groups like amine and carboxylic acids explain the formation of sp 2 domains and the concomitant loss of solubility. The annealed CD exhibit a broader and slightly red‐shifted emission band, with lower emission quantum yields, when compared to the initial nanohybrids.

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Publication Details

Journal
Small Structures
Published
2025-02-05
DOI
https://doi.org/10.1002/sstr.202400532
Citations
11
Primary Topic
Carbon and Quantum Dots Applications
Type
article
Field-Weighted Citation Impact
5.70

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article

Post‐Synthetic Graphitization and Photoluminescence Tuning of Carbon Dots from L‐Glutamic Acid

M. Ángeles Herranz, Nazario Martı́n, Laura Rodríguez‐Pérez, Andrés Ferrer‐Ruiz
11 citations
Small Structures
Carbon and Quantum Dots Applications
5.70
article

Post‐Synthetic Graphitization and Photoluminescence Tuning of Carbon Dots from L‐Glutamic Acid

M. Ángeles Herranz, Nazario Martı́n, Laura Rodríguez‐Pérez, Andrés Ferrer‐Ruiz
article en
11 citations

Abstract

Carbon dots are promising luminescent nanostructures. Their availability, based on inexpensive precursors and their intrinsic fluorescent nature, place them as potential choices against traditional quantum dots in some applications. However, the carbon dots nature is nowadays not well defined and understood. They are usually hybrid nanomaterials in terms of structure and composition, which hinders the knowledge of their photoluminescence mechanisms. Herein, the solvent‐free pyrolysis of L ‐glutamic acid by microwave synthesis leads to an incomplete graphitization of the precursor resulting in loose polymer‐like nanohybrids. Further experiments confirm that these carbon dots (CD) can be crosslinked and graphitized in a second heating step when using temperatures above 160 °C, reaching a plateau of graphitization over 200 °C. An exhaustive analysis by thermogravimetric analysis, Raman and X‐ray photoelectron spectroscopy highlights the structural changes undergo from 140 to 200 °C, where an increase of stability is observed due to the graphitization process. The condensation and decarboxylation reactions with loss of hydrophilic functional groups like amine and carboxylic acids explain the formation of sp 2 domains and the concomitant loss of solubility. The annealed CD exhibit a broader and slightly red‐shifted emission band, with lower emission quantum yields, when compared to the initial nanohybrids.

Small StructuresVol. 6(3)
Universidad Complutense de Madrid (ES), IMDEA Nanoscience (ES)
Comunidad de Madrid, European Commission, Ministerio de Ciencia e Innovación, Agencia Estatal de Investigación
Openalex Percentile: Top 4%
Carbon and Quantum Dots Applications
5.70
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Post‐Synthetic Graphitization and Photoluminescence Tuning of Carbon Dots from <i>L</i>‐Glutamic Acid — M. Ángeles Herranz, Nazario Martı́n, et al. · Small Structures (2025) | TGRS Research Map | TGRS