Chemical and Conformational Control of the Spectroscopic Properties of Multi-Layer and Multi-Defect Carbon Dots

Fuente: arXiv
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Main Authors: Mehmood, Arshad, Hetherington, Caitlin V., Zaidi, Zain, Levine, Benjamin G.
Format: Preprint
Published: 2025
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author Mehmood, Arshad
Hetherington, Caitlin V.
Zaidi, Zain
Levine, Benjamin G.
author_facet Mehmood, Arshad
Hetherington, Caitlin V.
Zaidi, Zain
Levine, Benjamin G.
contents Carbon dots (CDs) are renowned for their bright and tunable photoluminescence (PL), stability, and biocompatibility, yet it remains challenging to link their heterogeneous structures to their spectroscopic properties. This study utilizes density functional theory (DFT) and time-dependent DFT (TD-DFT) to systematically investigate how the spectroscopic properties of complex CDs with multiple layers and multiple defects are determined by their structures and compositions. Calculations reveal that strongly oxidizing defects, such as carbonyl and carbonyl acetate, significantly redshift absorption and emission spectra. In contrast, less oxidizing defects, such as hydroxyl, behave as spectators with minimal impact on absorption and emission, except when they interact strongly with more oxidizing defects. We find that not only the excitation energy but also the excitation character itself is impacted by the presence of specific defects, and the pH-dependence of the spectroscopic properties can be attributed to their protonation state-dependent excitation character. We show that the twisting, sliding, and linker-mediated folding of surface-functionalized layers in CDs markedly alter excitation energies and characters, offering a molecular explanation for experimentally observed emission intermittency and polarization fluctuations. These insights provide strategies for optimizing CDs for various applications, including bioimaging, photocatalysis, and optoelectronic devices.
format Preprint
id arxiv_https___arxiv_org_abs_2508_16520
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Chemical and Conformational Control of the Spectroscopic Properties of Multi-Layer and Multi-Defect Carbon Dots
Mehmood, Arshad
Hetherington, Caitlin V.
Zaidi, Zain
Levine, Benjamin G.
Chemical Physics
Mesoscale and Nanoscale Physics
Materials Science
Carbon dots (CDs) are renowned for their bright and tunable photoluminescence (PL), stability, and biocompatibility, yet it remains challenging to link their heterogeneous structures to their spectroscopic properties. This study utilizes density functional theory (DFT) and time-dependent DFT (TD-DFT) to systematically investigate how the spectroscopic properties of complex CDs with multiple layers and multiple defects are determined by their structures and compositions. Calculations reveal that strongly oxidizing defects, such as carbonyl and carbonyl acetate, significantly redshift absorption and emission spectra. In contrast, less oxidizing defects, such as hydroxyl, behave as spectators with minimal impact on absorption and emission, except when they interact strongly with more oxidizing defects. We find that not only the excitation energy but also the excitation character itself is impacted by the presence of specific defects, and the pH-dependence of the spectroscopic properties can be attributed to their protonation state-dependent excitation character. We show that the twisting, sliding, and linker-mediated folding of surface-functionalized layers in CDs markedly alter excitation energies and characters, offering a molecular explanation for experimentally observed emission intermittency and polarization fluctuations. These insights provide strategies for optimizing CDs for various applications, including bioimaging, photocatalysis, and optoelectronic devices.
title Chemical and Conformational Control of the Spectroscopic Properties of Multi-Layer and Multi-Defect Carbon Dots
topic Chemical Physics
Mesoscale and Nanoscale Physics
Materials Science
url https://arxiv.org/abs/2508.16520