The photophysical properties of a series of
-conjugated oligothiophene-perylene bisimide dyads
nT-PBI (
n= 1, 2, and 3) in solutions were investigated. A sharp fluorescence quenching of the perylene bisimide moietyin these dyads
nT-PBI (
n = 1, 2, and 3) was observed upon photoexcitation of the perylene bisimide moiety,indicating a fast and efficient electron-transfer process. The properties of photoinduced electron transfer ofthese dyads
nT-PBI (
n = 1, 2, and 3) in solutions were investigated by time-resolved fluorescence spectraand femtosecond transient absorption spectra in the visible region. It was found that as the number of thiophenerepeat units, i.e., the size, increases, the rate constants of charge separation and charge recombination increaseabout 3 orders and over 1 order of magnitude, respectively, because of the combined effects of energeticsand electronic coupling. These results demonstrate that a change in size of donor could change and modulatethe dynamics of electron transfer.