Bright near-infrared-emitting
Ag2S nanocrystals
(NCs)
are used for in vivo temperature sensing relying on a reversible variation
in intensity and photoluminescence lifetime within the physiological
temperature range. Here, to gain insights into the luminescence and
quenching mechanisms, we investigated the temperature-dependent luminescence
of Ag2S NCs from 300 to 10 K. Interestingly, both emission
and lifetime measurements reveal similar and strong thermal quenching
from 200 to 300 K, indicating an intrinsic quenching process that
limits the photoluminescence quantum yield at room temperature, even
for perfectly passivated NCs. The low thermal quenching temperature,
broadband emission, and multiexponential microsecond decay behavior
suggest the optical transition involves strong lattice relaxation,
which is consistent with the recombination of a Ag+-trapped
hole with a delocalized conduction band electron. Our findings offer
valuable insights for understanding the optical properties of Ag2S NCs and the thermal quenching mechanism underlying their
temperature-sensing capabilities.