The inner V2O5layer was introduced as a buffer layer to improve holes collection, while the outer V2O5layer served as a light coupling layer to enhance optical transmittance of the devic
Trang 1Semitransparent polymer solar cells using V 2 O 5 /Ag/V 2 O 5
as transparent anodes
Liang Shen⇑, Yang Xu, Fanxu Meng, Fumin Li, Shengping Ruan, Weiyou Chen
State Key Laboratory on Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, 2699 Qianjin Street,
Changchun 130012, People’s Republic of China
a r t i c l e i n f o
Article history:
Received 12 December 2010
Received in revised form 23 March 2011
Accepted 23 March 2011
Available online 6 April 2011
Keywords:
Semitransparent
Inverted
Transmittance
Reflectance
a b s t r a c t
We demonstrate semi-transparent inverted polymer solar cells with transparent anodes, made of Vanadium pentoxide (V2O5)/silver (Ag)/V2O5 The inner V2O5layer was introduced
as a buffer layer to improve holes collection, while the outer V2O5layer served as a light coupling layer to enhance optical transmittance of the device The transmittance and reflectance of V2O5(10 nm)/Ag (13 nm)/V2O5(x = 20, 40, 60, 80 nm) electrode are mea-sured and compared, and the dependence of the device performances on the thickness of the outer V2O5layer was investigated The results show that the maximum transmittance
of 90%, which appears from 400 to 700 nm, is obtained when the thickness of outer V2O5
layer is 40 nm
Ó 2011 Elsevier B.V All rights reserved
1 Introduction
During the past decade, polymer solar cells (PSCs) that
convert solar light directly into electricity have been
exten-sively investigated due to their advantage of low-cost,
flex-ible, and large area electronic devices [1–4] The most
recent progress[5–7] has addressed these concerns well
and the manufacture of PSCs on an industrial scale is
pos-sible and the operational stability is sufficient to allow for
demonstrations and round robins The power conversion
efficiency (PCE) of PSCs has recently achieved 6% or more
[8,9]in bulk heterojunction (BHJ) structure, where a
pho-toactive layer is composed of a mixture solution of
poly-meric electron donors (D) and soluble fullerene-based
electron acceptor (A) The light absorption can be
strength-ened by either using a thick active layer or developing low
bandgap polymers However, the short exciton diffusion
length and relatively low charge mobility in organic
semi-conductor materials limit the thickness within 100 nm
around[10] The limited use of the solar spectrum is also
a difficult problem to improve efficiency[11] One promis-ing way to achieve this is to use variable bandgap polymers
in a tandem structure in which multiple subcells with dif-ferent energy gaps are stacked, which uses a semitranspar-ent electrode to connect the front and back solar cells
[12,13] A variety of semitransparent electrode structures have been reported, but low transmittance and high series resistance exist universally to reduce the PCE[14,15] Here,
we report semitransparent inverted PSCs with a multilayer anode structure of V2O5/Ag/V2O5 V2O5, which is a kind of transition metal oxides, has been reported to enhance the performance of the polymer solar cells as an anodic buffer layer by Shrotriya et al.[16] Norrman et al.[17]have re-cently shown the PEDOT: PSS is the reason that very long lifetime PSCs (based on PEDOT) is unlikely to be possible
as some fatal degradation paths are linked to the active layer and edot interface So we get rid of PEDOT: PSS and manufacture the inverted PSCs The V2O5/Ag/V2O5is both optically transparent and suitable for holes collecting The inner V2O5layer is inserted between the active layer and Ag to serves as an anodic buffer layer to enhance holes collection The outer V2O5layer is used as a top-capping layer to enhance light coupling It would also lower the series resistance of PSCs
1566-1199/$ - see front matter Ó 2011 Elsevier B.V All rights reserved.
⇑Corresponding author.
E-mail address: shenliang@jlu.edu.cn (L Shen).
Contents lists available atScienceDirect
Organic Electronics
j o u r n a l h o m e p a g e : w w w e l s e v i e r c o m / l o c a t e / o r g e l
Trang 22 Experimental
The photovoltaic device has a structure of ITO/nc-TiO2/
RR-P3HT: PCBM/V2O5/Ag/V2O5, as shown schematically in
Fig 1 The ITO-conducting glass substrate (a sheet
resis-tance of 15X/hwas precleaned by acetone, ethanol, and
de-ionized water, respectively, for 15 min Anatase TiO2
thin films were prepared as described in our previous
pa-pers[18,19] The thickness of TiO2is 25 nm P3HT (Lumtec
Corp., used as received) was dissolved in
1,2-dichloroben-zene to produce 18 mg/ml solution, followed by blending
with PCBM (Lumtec Corp, used as received) in 1:1 weight
ratio[20] The blend was stirred for 72 h in the air before
spin coating on top of TiO2film surface Then the samples
were baked in low vacuum (vacuum oven) at 160°C or
20 min The typical film thickness of P3HT: PCBM is about
200 nm Finally 10 nm V2O5, 13 nm Ag, and x (x = 20, 40,
60, 80 nm) V2O5were thermally evaporated in sequence
under a high vacuum (5 104Pa) without disrupting
the vacuum The deposition rate was about 0.02 nm/s,
which was monitored with a quartz-oscillating thickness
monitor (ULVAC, CRTM-9000) The active area of the
de-vice was about 6.4 mm2
Current density–voltage (J–V) characteristics were
mea-sured with a computer-programmed Keithley 2400 source/
meter under AM1.5G solar illuminations with an Oriel
300 W solar simulator The intensity of the solar simulator
was 100 mW/cm2 The light intensity was measured with a
photometer (International light, IL1400) which was
cor-rected by a standard silicon solar cell The transmission
spectra and the reflection spectra were measured by
means of ultraviolet/visible spectrometer (UV 1700,
Shimadzu)
3 Results and discussion
Fig 2a shows the J–V characteristics of semitransparent
inverted polymer solar cells with outer 40 nm (device II)
and without V2O5 (device I) under AM1.5G illumination
of 100 mW/cm2 The incidence light irradiate from the
ITO side (Bottom) The detailed results are given inTable 1
Device I shows short circuit current density (Jsc) of
5.31 mA/cm2, open circuit voltage (Voc) of 0.590 V, fill fac-tor (FF) of 0.540, and power conversion efficiency (PCE) of 1.69 DeviceP shows Jscof 4.83 mA/cm2, Vocof 0.581 V,
FF of 0.606, PCE of 1.70 It can be seen that the PCE of device
I is almost same as that of device II The Jscof deviceP de-creases, but FF increases dramatically compared to that of device I We attribute the decrease of Jscto lower reflec-tance of V2O5/Ag/V2O5 from 400 to 650 nm, which is shown inFig 3b It is evident that the resistivity of the thin
Fig 1 The schematic structure drawing of the semitransparent inverted
Fig 2 The J–V characteristics of device ITO/nc-TiO 2 /P3HT: PCBM/V 2 O 5 (10 nm)/Ag (13 nm)/V 2 O 5 (x = 0, 40 nm) when illuminated from (a) ITO side and (b) V 2 O 5 /Ag/V 2 O 5 side.
Table 1 Characteristic data of semitransparent inverted polymer solar cells with different thickness of the V 2 O 5 capping layer illuminated from ITO (bottom) and V 2 O 5 /Ag/V 2 O 5 (top) side.
Device (nm) Illumination J sc (mA/cm2) V oc (V) FF (%) PCE (%)
Trang 3metal film (13 nm Ag here) is higher than that of the bulk
metal due to the scattering of the electrons from the
sur-face of the discontinuous film The outer V2O5decreases
the series resistance (Rsc), which is defined by the slope
of the J–V curve at J = 0 mA/cm2 The series resistance is
estimated to be 33.6X for device I and 23.3X for device
P The decrease of Rscresults in the increase of FF from
0.540 to 0.606 Fig 2b shows the J–V characteristics of
semitransparent inverted polymer solar cells (device I
andP) under AM1.5G illumination of 100 mW/cm2when
illuminated from V2O5/Ag/V2O5 side (Bottom) Here, the
mixture of P3HT and PCBM, which has main absorption
spectrum from 400 to 650 nm, is chosen as active layers
The photocurrent density is in direct proportion to light
absorption of the active layer Since devicePhas higher
transmittance from 400 to 650 nm, as shown inFig 3a, it
has bigger Jscthan device I
Fig 3a shows the transmittance spectra of the V2O5/Ag/
V2O5from 300 to 1000 nm It can be seen that the
trans-mittance becomes week with the increase of wavelength,
and high transmittance of 80% appears in short wavelength
range when the thickness of V2O5is zero When
introduc-ing outer VO (capping layer), the transmittance is
changed dramatically With the increase of the thickness
of V2O5 capping layer, the transmittance peaks are red-shifted The maximum transmittance of 90%, which ap-pears from 400 to 700 nm, is obtained when the thickness of V2O5 is 40 nm To continue increasing the thickness of V2O5, the transmittance gradually descends
It is evident that transmission can vary with the thickness
of the V2O5capping layer
Fig 3b shows the reflectance spectra of the V2O5/Ag/
V2O5from 300 to 1000 nm Since the absorption is little, the reflectance spectrum is nearly one to one complement with the transmittance spectrum It can be seen that reflectance peaks are redshifted gradually and would match better to the absorption spectra of the active layer (400–650 nm) when the thickness of the V2O5 capping layer increases
Fig 4a shows the the J–V characteristics of semitrans-parent inverted polymer solar cells under AM1.5G illumi-nation of 100 mW/cm2 when illuminated from ITO side (Bottom) The detailed results are given inTable 1 When the thickness of V2O5is 40 nm, the Jscis 4.83 mA/cm2, the
Vocis 0.581 V, the FF is 60.6%, and the PCE is 1.70% When
Fig 3 (a) The transmittance spectra of the transparent electrode V 2 O 5
(10 nm)/Ag (13 nm)/V 2 O 5 (x = 0, 20, 40, 60, 80 nm) (b) the reflectance
spectra of the transparent electrode V 2 O 5 (10 nm)/Ag (13 nm)/V 2 O 5 (x = 0,
20, 40, 60, 80 nm).
Fig 4 The J–V characteristics of device ITO/nc-TiO 2 /P3HT: PCBM/V 2 O 5 (10 nm)/Ag (13 nm)/V 2 O 5 (x = 20, 40, 60, 80 nm) dependent on the thickness of the V 2 O 5 capping layer when illuminated from (a) ITO side and (b) from V O /Ag/V O side.
Trang 4the thickness of V2O5is 80 nm, the photovoltaic device has
a Jscof 5.96 mA/cm2, Vocof 0.594 V, FF of 59.8%, and PCE of
2.12% The Jscof the device with 40 nm V2O5is the smallest;
and the Jscof the device with 80 nm V2O5is the biggest It is
known that the reflectance of the top electrode plays an
important role in trapping light for the active layer to
reab-sorb The reflectance of V2O5/Ag/V2O5(80 nm) from 400 to
650 nm is the strongest, but the reflectance of V2O5/Ag/
V2O5(40 nm) is poorest inFig 3b
Fig 4b shows the the J–V characteristics of
semitrans-parent inverted polymer solar cells under AM1.5G
illumi-nation of 100 mW/cm2 when illuminated from V2O5/Ag/
V2O5side (Top) The detailed results are given inTable 1
When the thickness of V2O5 is 40 nm, the Jscis 3.79 mA/
cm2, the Voc is 0.565 V, the FF is 60.6%, and the PCE is
1.30% When the thickness of V2O5is 80 nm, the
photovol-taic device has a Jscof 2.67 mA/cm2, Vocof 0.551 V, FF of
59.8%, and PCE of 0.88% The Jscof the device with 40 nm
V2O5 is the biggest, and that for the device with 80 nm
V2O5is the smallest This is because the transmittance of
V2O5/Ag/V2O5(40 nm) is the highest, and the absorption
of active layer material is directly proportional to the
transmittance of the incidence electrode When
illumi-nated from V2O5/Ag/V2O5 side, the Voc becomes smaller
compared with that illuminated from the ITO side The
dependence of the Vocand the photocurrent (Iph) can be
generally expressed as follows[21]:
Voc¼kT
q Log
Iph
Is þ 1
ð1Þ
Where Isis reverse saturation current, k is Boltzman
constant, T is the temperature, and q is charge Under Eq
(1), the Vocis directly proportional to Iph The Iphfrom ITO
side is much bigger than that from V2O5/Ag/V2O5 side,
which is shown inTable 1
4 Conclusion
In summary, we present efficient semi-transparent
in-verted polymer solar cells with highly transparent V2O5/
Ag/V2O5anodes The inner V2O5layer was introduced as
a buffer layer to improve holes collection, while the outer
V2O5 served as a light coupling layer to enhance optical
transmittance The incident light transmittance changed
with the thickness of V2O5.When the thickness of V2O5is
40 nm, the highest transmittance is obtained The reflec-tance peaks are redshifted gradually and would match bet-ter to the absorption spectra of the P3HT: PCBM layer when the thickness of the V2O5capping layer increases Acknowledgements
The authors are grateful to Major Project of Science and Technology Development Plan of Jilin Provincial Science and Technology Department (Grant Nos 20070402,
20080330, 20100103), the China 863 Program (Grant No 2007AA03Z406, 2009AA032402), Scientific Frontier and Interdiscipline Innovative Projects of Jilin University (Grant Nos 200903087), National Natural Science Foundation of China (Grant Nos 60977031, 50977038, 61007022,
61077046, 61006013) and Doctoral Found of Ministry of Education of China Grant Nos 20090061110040,
20100061120045 for the support to the work
References
[1] M Helgesen, R Søndergaard, F.C Krebs, J Mater Chem 20 (2010) 36 [2] F.C Krebs, Sol Energy Mater Sol Cells 93 (2009) 394.
[3] C Deibel, V Dyakonov, Rep Prog Phys 73 (2010) 096401 [4] R Po, M Maggini, N Camaioni, J Phys Chem C 114 (2010) 695 [5] F.C Krebs, T.D Nielsen, J Fyenbo, M Wadstrøm, M.S Pedersen, Energy Environ Sci 3 (2010) 512.
[6] F.C Krebs, J Fyenbo, M Jørgensen, J Mater Chem 20 (2010) 8994 [7] F.C Krebs, T Tromholt, M Jørgensen, Nanoscale 2 (2010) 873 [8] S.H Park, A Roy, S Beaupré, S Cho, N Coates, J.S Moon, D Moses, M Leclerc, K Lee, A.J Heeger, Nat Photonics 3 (2009) 297.
[9] H.Y Chen, J Hou, S Zhang, Y Liang, G Yang, Y Yang, L Yu, Y Wu, G.
Li, Nat Photonics 3 (2009) 649.
[10] P Peumans, A Yakimov, S.R Forrest, J Appl Phys 93 (2003) 3693 [11] G Dennler, M C Scharber, C J Brabec, Adv Mater 21 (2009) 1323 [12] T Ameri, G Dennler, C Lungenschmied, C J Brabec, Energy Environ Sci 2 (2009) 347.
[13] J Gilot, M.M Wienk, R.A.J Janssen, Appl Phys Lett 90 (2007) 143512.
[14] F.C Chen, J.L Wu, K.H Hsieh, W.C Chen, S.W Lee, Org Electron 9 (2008) 1132.
[15] G.M Ng, E.L Kietzke, T Kietzke, L.W Tan, P.K Liew, F.R Zhu, Appl Phys Lett 90 (2007) 103505.
[16] V Shrotriya, G Li, Y Yao, C Chu, Y Yang, Appl Phys Lett 88 (2006) 073508.
[17] K Norrman, M.V Madsen, S.A Gevorgyan, F.C Krebs, J Am Chem Soc 132 (2010) 16883.
[18] C Tao, S.P Ruan, X.D Zhang, G.H Xie, L Shen, X.Z Kong, W Dong, C.X Liu, W.Y Chen, Appl Phys Lett 93 (2008) 193307.
[19] L Shen, G.H Zhu, W.B Guo, C Tao, X.D Zhang, C.X Liu, W.Y Chen, S.P Ruan, Z.C Zhong, Appl Phys Lett 92 (2008) 073307 [20] V Shrotriya, G Li, Y Yao, T Moriarty, K Emery, Y Yang, Adv Funct Mater 16 (2006) 2016.
[21] A Moliton, J.M Nunzi, Polym Int 55 (2006) 583.