Comment on "Interface state recombination in organic solar cells"

In a recent paper, Street et al. [Phys. Rev. B 81, 205307 (2010)] propose first order recombination due to interface states to be the dominant loss mechanism in organic bulk heterojunction solar cells, based on steady-state current--voltage characteristics. By applying macroscopic simulations, we found that under typical solar cell conditions, monomolecular or bimolecular recombination cannot be inferred from the slope of the light intensity dependent photocurrent. In addition, we discuss the validity of calculating a mobility--lifetime product from steady-state measurements. We conclude that the experimental technique applied by Street et al. is not sufficient to unambiguously determine the loss mechanism.Comment: 4 pages, 2 figures. Corrected Eqns. (2) and (4): 1/... was missin

Investigation of electronic trap states in organic photovoltaic materials by current-based deep level transient spectroscopy

Current-based deep level transient spectroscopy was used to study trap states in poly(3- hexylthiophene-2,5-diyl) (P3HT), [6,6]-phenyl-C61 butyric acid methyl ester (PCBM) and P3HT:PCBM blend. The obtained spectra showed traps of 87 meV activation energy in pure P3HT and 21 meV for PCBM. The blend shows a complex emission rate spectrum consisting of several different emission rate bands in the range of (0.1-30) s^-1, yielding activation energies between about 30 meV and 160 meV.Comment: 4 pages, 3 figure