Carbon
dots (CDs) are low-dimensional luminescent carbon materials
with novel and tunable surface-dependent properties. Interfacial charge
transfer is the fundamental principle mostly accountable for their
extensive usage in catalysis and optoelectronics; however, this phenomenon
remains mostly underexplored to date. Herein, we inspect the impact
of cationic and anionic surfactants, encapsulation, and Coulombic
interactions on the photoinduced interfacial charge-transfer kinetics
between CDs and vitamin K3 (MQ). With a series of singlet and triplet
state measurements, we have identified the transient intermediates,
connoting the occurrence of excited-state electron transfer (ET) and
hydrogen atom transfer (HAT) between the two. The strong electrostatic
attraction between the cetyl trimethyl ammonium bromide micellar head
groups and CDs enhances ET, while in the sodium dodecyl sulfate micellar
medium, HAT is preferable. With an external magnetic field (MF) equivalent
to the order of hyperfine interactions, we confirm the occurrence
of both ET and HAT in triplet CDs and MQ and observe that their rates
are significantly modulated not only by encapsulation but also by
Coulombic interactions between the charged micellar interface and
CDs. However, in the aqueous medium, the signature of charge-transfer
products is very minimal even in the presence of the MF and is mostly
indistinguishable within the measured time limit.