posted on 2019-05-03, 00:00authored bySebastian Pont, Silvio Osella, Alastair Smith, Adam V. Marsh, Zhe Li, David Beljonne, João T. Cabral, James R. Durrant
In polymer/fullerene
organic solar cells, the photochemical dimerization
of phenyl-C61-butyric acid methyl ester (PCBM) was reported
to have either a beneficial or a detrimental effect on device performance
and stability. In this work, we investigate the behavior of such dimers
by measuring the temperature dependence of the kinetics of PCBM de-dimerization
as a function of prior light intensity and duration. Our data reveal
the presence of both “weakly” and “strongly”
bound dimers, with higher light intensities preferentially generating
the latter. DFT simulations corroborate our experimental findings
and suggest a distribution of dimer binding energies, correlated with
the orientation of the fullerene tail with respect to the dimer bonds
on the cage. These results provide a framework to rationalize the
double-edged effects of PCBM dimerization on the stability of organic
solar cells.