posted on 2014-07-31, 00:00authored bySandra Jenatsch, Roland Hany, Anna C. Véron, Martin Neukom, Simon Züfle, Andreas Borgschulte, Beat Ruhstaller, Frank Nüesch
Bilayer organic solar cells based
on trimethine cyanine donor and
C60 acceptor materials have been fabricated by coating
the trimethine dye from solution on molybdenum oxide (MoO3) anode buffer layer. The choice of deposition solvent drastically
influences device performance, with 2,2,3,3-tetrafluoro-1-propanol
(TFP) reducing the fill factor and power conversion efficiency of
the device by 36 and 21%, respectively, as compared to chlorobenzene.
In the case of TFP, extraction of photogenerated charge carriers by
linearly increasing voltage (photo-CELIV) and capacitance–voltage
analysis revealed the formation of a hole trapping zone at the molybdenum
oxide interface which is also responsible for the S-shape current–voltage
curve under white light irradiation. The transient charge extraction
signal originating from trapped holes at the MoO3 interface
could be clearly distinguished from the one relating to hole mobility
in cyanine films using photo-CELIV measurements with varying delay
times.