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Effects of Photo‐oxidation on the Performance of Poly[2‐methoxy‐5‐(3′,7′‐dimethyloctyloxy)‐1,4‐phenylene vinylene]:[6,6]‐Phenyl C 61 ‐Butyric Acid Methyl Ester Solar Cells
Author(s) -
Pacios R.,
Chatten A. J.,
Kawano K.,
Durrant J. R.,
Bradley D. D. C.,
Nelson J.
Publication year - 2006
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.200500714
Subject(s) - photocurrent , materials science , photodegradation , organic solar cell , phenylene , absorption (acoustics) , photochemistry , polymer solar cell , photoactive layer , active layer , poly(p phenylene vinylene) , solar cell , polymer , layer (electronics) , optoelectronics , organic chemistry , chemistry , electroluminescence , nanotechnology , composite material , photocatalysis , catalysis , thin film transistor
A study of the photo‐oxidation of films of poly[2‐methoxy‐5‐(3′,7′‐dimethyloctyloxy)‐1,4‐phenylene vinylene] (MDMO‐PPV) blended with [6,6]‐phenyl C 61 ‐butyric acid methyl ester (PCBM), and solar cells based thereon, is presented. Solar‐cell performance is degraded primarily through loss in short‐circuit current density, J SC . The effect of the same photodegradation treatment on the optical‐absorption, charge‐recombination, and charge‐transport properties of the active layer is studied. It is concluded that the loss in J SC is primarily due to a reduction in charge‐carrier mobility, owing to the creation of more deep traps in the polymer during photo‐oxidation. Recombination is slowed down by the degradation and cannot therefore explain the loss in photocurrent. Optical absorption is reduced by photo‐bleaching, but the size of this effect alone is insufficient to explain the loss in device photocurrent.