All-plastic solar cells with a high photovoltaic
dynamic range†
Yinhua Zhou, Talha M. Khan, Jae Won Shim, Amir Dindar, Canek Fuentes-Hernandez
and Bernard Kippelen
*
We report on semitransparent air-processed all-plastic solar cells, fabricated from vacuum-free processes,
comprising two polymer electrodes, a polymeric work-function modification layer and a polymer:fullerene
photoactive layer. The active layer and the top PEDOT:PSS electrode were prepared by sequential film-
transfer lamination on polyethylenimine-modified PEDOT:PSS bottom electrodes. The transferring of
films offers ease of layer patterning and the misalignment of defects in the different layers resulting from
the additive film transfer lamination process yields high shunt resistance values of 10
8
ohm cm
2
.
Consequently, all-plastic solar cells fabricated with this process exhibit very low reverse bias dark current
and can operate in the photovoltaic quadrant with light irradiance varying over five orders of magnitude.
The analysis of the values of the open-circuit voltage as a function of light irradiance over that wide
dynamic range points toward an ideality factor of n ¼ 1.82 and a reverse saturation current density of
6.2 10
11
A cm
2
for solar cells with an active layer comprised of a blend of poly(3-hexylthiophene)
and an indene fullerene bis-adduct.
Organic solar cells are attractive because of their potential for
low cost fabrication, light weight, and excellent mechanical
exibility.
1–10
Currently, most common organic solar cells are
fabricated on indium tin oxide (ITO) coated glass substrates
with vacuum-deposited evaporated metals used as the top
electrodes. To realize the full potential for low cost, ITO-free
organic solar cells should preferably be fabricated using
vacuum-free processes in ambient air.
11–13
Recently, we reported
all-plastic solar cells comprising polymer electrodes: poly(3,4-
ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)
and active layer: poly(3-hexylthiophene) (P3HT):indene-C
60
bis-
adduct (ICBA).
1
These all-plastic solar cells were fully processed
in air from solutions of orthogonal solvents using spin coating.
In these devices, the solvent used to process the active layer,
typically chlorobenzene or dichlorobenzene, allows for water-
based solutions of the conducting polymer PEDOT:PSS to be
deposited on top with minimum damage of the layer under-
neath but wetting issues can be a challenge.
Film-transfer lamination is a method of lm preparation
wherein a lm is rst deposited on a carrier substrate (typically
crosslinked polydimethylsiloxane, PDMS), and is then lami-
nated onto the target substrate with the carrier substrate. The
carrier is nally peeled away to nish the lm transfer. Transfer
lamination is a dry process and avoids wetting issues and lm
damage arising from the use of non-orthogonal solvents during
spin coating, ink-jet printing or any other additive wet-deposi-
tion method. The lm-transfer lamination technology has been
used to prepare top metal electrodes,
14
PEDOT:PSS
15,16
and
active layers
17,18
in organic light-emitting diodes and organic
solar cells. Because of the solvent-free dry process used during
the transfer lamination, this technique was used to construct
multi-layer organic lms as the active layer.
19–21
It was also used
to modulate the vertical phase segregation in P3HT:ICBA to
study its effect on solar cell performance.
22,23
Another important
advantage of the lm-transfer lamination technique is the ease
in patterning the top PEDOT:PSS electrode as compared to the
spin coating technique.
In this work, we report on the rst demonstration of semi-
transparent all-plastic solar cells fabricated in ambient air by
sequential dry lm-transfer lamination of a P3HT:ICBA photo-
active layer and a PEDOT:PSS (high conductivity formulation,
PH1000) top electrode. Fig. 1a shows the device structure of the
solar cells. The bottom electrode is comprised of a patterned
PH1000 lm, modied by a thin layer of polyethylenimine (PEI).
PEI modication has been proven to improve the electron
collection and performance of various types of solar cells by
signicantly reducing the work function of the underlying
conductor.
1,24–30
The P3HT:ICBA and PH1000 lms are respec-
tively used as the active layer and the top electrode, and are
prepared by lm-transfer lamination. These layers are hereby
referred to as P3HT:ICBA-L and PH1000-L. Fig. 1b illustrates the
procedure for fabrication of the all-plastic solar cells. This
Center for Organic Photonics and Electronics (COPE), School of Electrical and
Computer Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
E-mail: kippelen@ece.gatech.edu
† Electronic supplementary information (ESI) available. See DOI:
10.1039/c3ta15073a
Cite this: J. Mater. Chem. A, 2014, 2,
3492
Received 6th December 2013
Accepted 17th January 2014
DOI: 10.1039/c3ta15073a
www.rsc.org/MaterialsA
3492 | J. Mater. Chem. A, 2014, 2, 3492–3497 This journal is © The Royal Society of Chemistry 2014
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