The perennial problem of instability
of fluorescent copper nanoclusters
(Cu NCs), stemming principally from aerial oxidation, has prevented
their vivid usage in energy harvesting compared to the other metal
NCs. However, replacement of the much expensive metal NCs with the
cheaper Cu NCs is desirable if the functions are met with. Although
thiolate protection of Cu NCs could bring some stability to them,
appreciably decentlystable Cu NCs were produced inside the aqueous
core of reverse micelles (RMs). However, this recent development has
not been further explored on the photosensitization of the Cu NCs
inside the RMs and their controlled modulation as energy antenna.
Here we have synthesized stable Cu NCs inside the aqueous core of
RMs with three different pool sizes and established photoinduced electron
transfer (PET) to an electron acceptor. Considering the bulk quencher
concentration, it appears that the extent of PET increases with decrease
in the size of the aqueous core of RMs. However, calculating the effective
concentration of the electron acceptor inside the RMs and considering
the polarity of the microheterogeneous systems, it becomes clear that
the extent of PET actually decreases with decrease in the size of
the aqueous pool (w
0, i.e., [H2O]/[AOT]) = 5–20) in the RMs. This proof of concept and the
results are promising toward applications in PET-driven phenomena
such as solar cells or batteries.