Authors
Umarfaruk S Sayyad, Sapna Waghmare, Himanshu Bhatt, Payal Swami, Hirendra N Ghosh, Somen Mondal
Published in
Nanoscale. Aug 05, 2026. Epub Aug 05, 2026.
Abstract
Photobases are materials that exhibit enhanced basicity in their excited states and play a significant role in applications such as photocatalytic chemical transformations, water splitting, and polymerization. In this study, we investigated the photobasicity of excitation dependent full color light emitting carbon Dots (C-Dots) and examined the role of nitrogen sites, specifically pyridinic, pyrrolic, and graphitic nitrogen in the core, along with various electron-donating (-NH2) and electron-withdrawing (-COOH) surface functional groups in regulating their photobase characteristics. Exploring the photobasic properties and proton transfer pathways of differently emitting C-Dots is challenging due to their complex internal structure. To address this, the ground- and excited-state pKa values, along with the protonation sites of different emitting C-Dots, were first determined using pH-metric titration. Furthermore, optical studies were carried out to investigate the photobase properties of the C-Dots. The combined results suggest the protonation pathways in various emitting C-Dots. In B-C-Dots, proton abstraction occurs directly at the core from water, whereas in G-C-Dots and R-C-Dots, protonation occurs with the assistance of functional groups present on the surface of the C-Dots upon the photoexcitation of C-Dots. Ultrafast spectroscopic measurements reveal that proton transfer occurs in different emitting C-Dots within 180-480 fs after excitation, with the fastest process observed in G-C-Dots at approximately 185 fs. Therefore, this study provides a strategy for controlling the photobasicity of C-Dots, which may open up promising applications in related fields.
PMID:
42555869
Bibliographic data and abstract were imported from PubMed on 06 Aug 2026.
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