Femtosecond transient absorption spectral (TAS) investigations
were performed to understand the carrier relaxation mechanism for
perovskite nanocrystals Cs1–x
FA
x
PbBr3 (CF, x =
0.45) and CsPbBr3 (CS), which served as efficient photocatalysts
for splitting of CO2 into CO and O2 in the absence
of water. Upon light irradiation for 12 h, formation of deep trap
states was found for both CS and CF samples with spectral characteristics
of the TAS photobleach (PB) band showing a long spectral tail extending
to the long wavelength region. The charge recombination rates at the
shallow surface states, bulk states, and deep-trapped surface state
were found to be significantly retarded for the CF sample than for
the CS sample, in agreement with the photocatalytic performances for
CO product yields of the CF catalyst being greater by a factor of
3 compared to those of the CS catalyst.