Methyl-substituted
germanane is an emerging material that has been
proposed for novel applications in optoelectronics, photoelectrocatalysis,
and biosensors. It is a two-dimensional semiconductor with a strong
above-gap fluorescence associated with water intercalation. Here,
we use time-resolved photoluminescence spectroscopy to understand
the mechanism causing this fluorescence. We show that it originates
from two distinct exciton populations. Both populations recombine
exponentially, accompanied by the thermally activated transfer of
exciton population from the shorter- to the longer-lived type. The
two exciton populations involve different electronic levels and couple
to different phonons. The longer-lived type of exciton migrates within
the disordered energy landscape of localized recombination centers.
These outcomes shed light on the fundamental optical and electronic
properties of functionalized germanane, enabling the groundwork for
future applications in optoelectronics, light harvesting, and sensing.