MEH-PPV and PCBM Solution Concentration Dependence of Inverted-Type Organic Solar Cells Based on Eosin-Y-Coated ZnO Nanorod Arrays

Ginting, Riski Titian; Yap, Chi Chin; Yahaya, Muhammad; Mat Salleh, Muhamad

doi:https://doi.org/10.1155/2013/503715

International Journal of Photoenergy

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Organic Electronics

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Research Article | Open Access

Volume 2013 | Article ID 503715 | https://doi.org/10.1155/2013/503715

MEH-PPV and PCBM Solution Concentration Dependence of Inverted-Type Organic Solar Cells Based on Eosin-Y-Coated ZnO Nanorod Arrays

Riski Titian Ginting,¹Chi Chin Yap,¹Muhammad Yahaya,¹and Muhamad Mat Salleh²

Academic Editor: Manoj A. G. Nambuthiry

Received01 Aug 2012

Revised29 Nov 2012

Accepted29 Nov 2012

Published08 Jan 2013

Abstract

The influence of polymer solution concentration on the performance of chlorobenzene- (CB-) and chloroform- (CF-) based inverted-type organic solar cells has been investigated. The organic photoactive layers consisted of poly(2-methoxy-5-(2-ethyl hexyloxy)-1,4-phenylenevinylene) (MEH-PPV) and (6,6)-phenyl C₆₁ butyric acid methyl ester (PCBM) were spin coated from CF with concentrations of 4, 6, and 8 mg/mL and from CB with concentrations of 6, 8, and 10 mg/mL onto Eosin-Y-coated ZnO nanorod arrays (NRAs). Fluorine doped tin oxide (FTO) and silver (Ag) were used as electron collecting electrode and hole collecting electrode, respectively. Experimental results showed that the short circuit current density and power conversion efficiency increased with decrease of solution concentration for both CB and CF devices, which could be attributed to reducing charge recombination in thinner photoactive layer and larger contact area between the rougher photoactive layer and Ag contact. However, the open circuit voltage decreased with decreasing solution concentration due to increase of leakage current from ZnO NRAs to Ag as the ZnO NRAs were not fully covered by the polymer blend. The highest power conversion efficiencies of % and % were achieved at the respective lowest solution concentrations of CB and CF.

1. Introduction

Rapid development in enhancing the performance of organic solar cells (OSCs) for the past few years by utilizing bulk heterojunction (BHJ) devices has enabled power conversion efficiency (PCE) up to 10.6% to be achieved [1]. In the case of BHJ conventional device structure, an active layer which consists of polymer donor and acceptor material is normally sandwiched between indium tin oxide (ITO) anode and aluminium (Al) cathode [2]. Poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) or PEDOT:PSS which plays role as conductive hole transport layer (HTL) is commonly introduced in between organic photoactive layer and ITO anode [3]. However, due to strong acidic nature of PEDOT:PSS, instability between the interface of ITO/PEDOT:PSS could create defect site and thus leading to deteriorated device performance [4, 5]. Moreover, oxidation of low work function Al electrode (4.28 eV) in air could also lead to instability at the interface between metal and organic photoactive layer [6]. In order to solve these issues, inverted configuration with low work function metal or metal oxides materials as electron transporting layer and high work function metal (e.g., silver, gold) as hole collection electrode have been introduced to improve the stability of the device [6, 7]. Lately, a lot of attention towards inverted OSCs with various metal oxide nanostructures as electron transporting layer have been developed, such as ZnO [8–14], TiO₂ [15–19], alkali-metal oxide cesium carbonate (Cs₂CO₃) [20, 21], and others [22, 23]. The environmental-friendly and low-cost ZnO nanorods arrays (NRAs) can be grown at low temperature (below 100°C) by hydrothermal method [24]. The ZnO NRAs not only have good electron collecting and transporting property in the inverted OSCs hybridized with the polymer blend, but also can provide larger interface surface area to improve photocurrent and efficiency [25].

Recently, much effort has been focused on utilizing blend film of poly(3-hexylthiophene) (P3HT) and (6,6)-phenyl C₆₁ butyric acid methyl ester (PCBM) as photoactive layer in ZnO NRAs-based inverted OSCs [19–23]. Various P3HT-PCBM processing parameters such as solvent selection, solution concentration, and spin coating speed have been investigated to optimize the solar cell performance [25, 26]. Takanezawa et al. [25] reported that thicker organic photoactive layer deposited by using higher solution concentration or lower spin coating speed results in better power conversion efficiency as a consequence of improved optical absorption and short circuit current density. Meanwhile, Chou et al. [26] demonstrated that organic photoactive layer drying time could be lengthened by lowering the spin coating speed, hence leading to improved photovoltaic performance as a result of better polymer crystallinity, increased thickness, and enhanced infiltration of photoactive layer. However, little attention has been given to poly[2-methoxy-5-(2′-ethylhexyloxy)-p-phenylenevinylene] (MEH-PPV) blended with PCBM as photoactive layer in the similar OSCs. MEH-PPV has broad optical absorption region 400–600 nm and also higher hole mobility compared to electron mobility [27].

The present work reports on the effects of MEH-PPV and PCBM solution concentration on the performance of inverted-type OSCs based on Eosin-Y-coated ZnO NRAs. Eosin-Y organic dye, a low-cost alternative to expensive Ru-complexes dye, has good absorption property and is able to increase the wettability of ZnO surface [28]. Different solution concentrations of MEH-PPV and PCBM were prepared from chlorobenzene (CB) and chloroform (CF). The short circuit current density and power conversion efficiency increased, whereas the open circuit voltage decreased with the reduction of solution concentration. The optimum power conversion efficiencies of 0.54 ± 0.10% and 0.87 ± 0.15% were achieved at the respective lowest solution concentration of CB and CF devices.

2. Experimental Methods

2.1. Device Fabrication

Inverted OSCs with fluorine doped tin oxide (FTO)/Eosin-Y-coated ZnO NRAs/MEH-PPV and PCBM(1:2)/Ag structure were constructed. The FTO (~15 /sq) substrates were ultrasonically cleaned by using acetone and 2-propanol each for 15 min. The ZnO seed layer was spin coated on top of precleaned substrates for 3 times from an equimolar solution (0.2 M) of zinc acetate dehydrate (Zn(O₂CCH₃)₂·(H₂O)₂) and diethanolamine (DEA) in ethanol followed by annealing at 300°C for one hour in air. The hydrothermal growth of ZnO NRA was done by immersing ZnO seed coated substrates into an equimolar aqueous solution (40 mM) of zinc nitrate hexahydrate (Zn(NO₃)₂·6H₂O) and hexamethylenetetramine (HMT) at 90°C for 45 min in a laboratory oven. The dye coating was performed by spin coating a thin layer of Eosin-Y from a 0.3 mM acetone solution onto ZnO NRAs. The MEH-PPV with molecular weight 40,000–70,000 g mol⁻¹ and PCBM were purchased from Sigma-Aldrich and Nano-C, respectively. MEH-PPV and PCBM (1:2 by weight) were dissolved in two different solvents, namely chloroform (CF) and chlorobenzene (CB) at various concentrations. CF solutions with concentration of 4 mg/mL to 8 mg/mL and CB solutions with concentration of 6 mg/mL to 10 mg/mL were spin-coated on top of Eosin-Y-coated ZnO NRAs. The spinning speed and spinning time were fixed at 1000 rpm and 60 s, respectively. Finally, the silver (Ag) contact (200 nm) was deposited by using magnetron sputtering under vacuum (~10⁻³ Torr) by flowing Argon (Ar) gas at 45 cc/min. During sputtering process, a slow deposition rate ~0.17 nm s⁻¹ was used in order to avoid the damage of organic photoactive layer. Furthermore, in order to oxidize silver, pure oxygen gas was introduced during sputtering process into the vacuum chamber at a flow rate of 5 cc/min. It was believed that oxidation of Ag will increase its work function from 4.3 to 5.0 eV, which in turn facilitate hole collection from donor materials to Ag and improve the cells performance [29]. Four devices for each solution concentration were fabricated.

2.2. Device Characterization

The absorption spectra of blend films consisted of organic photoactive layer and Eosin-Y-coated ZnO NRAs were investigated using a Perkin Elmer Lambda 900 UV-Vis spectrophotometer. The cross-sectional images of organic photoactive layer deposited on Eosin-Y-coated ZnO NRAs were recorded by using Carl Zeiss Supra 55VP Field Emission Scanning Electron Microscope (FESEM). The surface morphology of the organic photoactive layers was investigated by using Ntegra Prima NT-MDT scanning probe microscope under ambient condition at %RH ~68% and room temperature 26°C. The characteristics of the devices were measured with Keithley 237 SMU under illumination at 100 mW/cm² from a solar simulator with AM 1.5 G filter. The active area of the devices was defined as 0.07 cm² by using mask. The incident photon to current conversion efficiency (IPCE) values was measured using Newport IPCE system at a chopping frequency of 10 Hz. The above device fabrication and measurements were conducted under ambient atmosphere (without encapsulation).

3. Results and Discussion

Figure 1 shows the optical absorption properties of blend films of organic photoactive layer and Eosin-Y-coated ZnO NRAs. Broad absorption from 400 nm up to 600 nm is correlated with MEH-PPV [30], whereas absorption below 400 nm is contributed by PCBM and ZnO NRAs [31]. The absorption increased with solution concentration for both CF and CB. It has been reported that enhanced absorption in the long wavelength range of the polymer indicates the increase in crystallinity and hole mobility of the polymer [32]. However, the shape of absorption spectra of MEH-PPV and PCBM blend film (in the range of 400–600 nm) showed no notable changes with different solvents and solution concentration, suggesting no significant different in crystallinity and hole mobility of the polymer. The Eosin-Y-coated ZnO NRAs exhibited absorption in visible region from 440 nm to 560 nm (inset of Figure 1) and two absorption peaks at 500 nm and 530 nm corresponding to the monomeric and dimeric forms of Eosin-Y were observed [33]. The intensity of Eosin-Y absorption was much lower than that of MEH-PPV, suggesting Eosin-Y had a little contribution to the overall absorption of device. However, the existence of thin layer dye on top of ZnO NRAs may enhance the charge transfer efficiency at the MEH-PPV/ZnO NRAs interface and also improve the wetting state of ZnO NRAs [34].

(a)

(b)

Figure 2 shows typical cross-sectional images of devices prepared from CB and CF at different concentrations. ZnO nanorods with diameter ranging from 50 nm to 80 nm and with length up to 300 nm were obtained. The total thickness of the blend films prepared from CB and CF reduced from ~560 nm to ~460 nm and from ~500 nm and ~400 nm, respectively, with decrease of solution concentration. This is consistent with absorption result shown above where the absorption increased with increasing solution concentration, indicating formation of thicker blend film. In addition, it can be clearly seen that the infiltration of organic blend prepared from CB into the spacing between Eosin-Y-coated ZnO nanorods was better than that prepared from CF, as indicated by the increased number of voids appeared in the interspaces between ZnO nanorods. The polymer prepared from a higher boiling point solvent has longer time to effectively infiltrate into the spacing between ZnO nanorods and gives enough time for polymer chain to self-organized [35]. Therefore, the poor infiltration could be attributed to lower boiling point of CF (~61°C) as compared to CB (~131°C).

(a)

(b)

(c)

(d)

The characteristics of typical devices under illumination of a simulated AM 1.5 sunlight at 100 mW/cm² are shown in Figure 3(a), whereas the statistical data for photovoltaic parameters obtained from a series of four individual devices for each parameter are plotted in Figure 3(b). The short-circuit current density (), fill factor (FF) and power conversion efficiency (PCE) increased with decreasing solution concentration for both CB- and CF-based devices, whereas the open circuit voltage () exhibited opposite behavior. Both CB- and CF-based devices showed the highest PCE at respective lowest solution concentration. The device prepared from CB at concentration of 6 mg/mL exhibited the highest PCE of 0.54 ± 0.10% with of 3.45 ± 0.17 mA cm⁻², of 0.34 ± 0.02 V and FF of 0.48 ± 0.02. In the case of CF, the highest PCE of 0.87 ± 0.15% was achieved at the concentration of 4 mg/mL, with of 4.76 ± 0.17 mA cm⁻², of 0.35 ± 0.03 V, and FF of 0.51 ± 0.02. However, further reduction of polymer solution concentration results in very low V and low mA cm⁻² for both CB and CF devices (not shown here). The series resistance () and shunt resistance () were determined from the slopes at and in the curve, respectively. The enhancement of with decreasing solution concentration could be correlated with the organic photoactive layer thickness. It is generally accepted that increase in thickness results in more excitons due to higher absorption. However, the charge recombination rate also increases with thickness, resulting in lower . In contrast to study obtained on P3HT and PCBM-based inverted-type organic solar cell [25], increase in thickness did not lead to increase in , but to a decrement in present work. This suggests that charge recombination process dominated the variation of with respect to thickness. It is believed that the probability of photogenerated electrons and holes to transport to ZnO NRAs and Ag, respectively, became higher with thinner photoactive layer. The decreased significantly from 397.24 ± 30.87 to 25.40 ± 6.91 cm² and from 220.26 ± 11.53 to 15.97 ± 2.47 cm² as the polymer solution concentration reduced for CB and CF devices, respectively. This result indicates the decrease of bulk resistance across the organic photoactive layer with decreasing thickness, leading to higher number of electron and hole extracted from the device. Besides, the increase of with the solution concentration for both solvents could be due to suppression of leakage current as indicated by larger . The significant decrement of with respect to leads to increment in FF. Therefore, the increase in both and FF was great enough to offset the reduced , which in turn improved the overall device performance. The overall photovoltaic performance of all devices is summarized in Table 1.

Figure 4 shows IPCE spectra of the devices measured from wavelength 350 to 800 nm with maximum IPCE of ~16% and ~20% at 500 nm was achieved at respective lowest solution concentration for CB and CF device. Despite the increase of absorption with solution concentration, the opposite trend was observed from IPCE spectra. The IPCE result is consistent with which increased with decreasing solution concentration and further confirms that relatively thick organic photoactive layer on top of Eosin-Y-coated ZnO NRAs causes the increase of charge recombination in the organic photoactive layer and results in lower even though the absorption increased. The IPCE spectra of the CB and CF devices with the highest solution concentration exhibited low photon conversion efficiency at wavelength (500 nm) corresponding to absorption peak of MEH-PPV. For thicker photoactive layer deposited at high solution concentration, most of the photons with wavelength close to 500 nm were absorbed in the region close to FTO/Eosin-Y-coated ZnO NRAs. Meanwhile, photons with wavelength away from 500 nm were more uniformly absorbed throughout the photoactive layer. The distortion of IPCE spectrum of thick photoactive layer indicates that photocurrent generation in the bulk region close to Ag was more efficient than that in the region close to ZnO NRAs [36]. This result also suggests that the probability of holes generated in the region close to ZnO NRAs to be trapped or recombine before reaching Ag was higher.

(a)

(b)

Figure 5 shows the topographic images of surface morphology of organic photoactive layer deposited on Eosin-Y-coated ZnO NRAs with different solvent concentrations. The root mean square (rms) roughness significantly increased from 2.58 to 14.75 nm and from 4.11 to 17.77 nm, respectively, as the CB and CF solution concentration decreased. The rough surface obtained from lower solution concentration indicates ZnO NRAs were not fully covered by polymer blend. This finding is in agreement with the value of which increased with solution concentration. Besides, this observation is also well in line with the cross-sectional FESEM images from which a wavy surface reflecting the ZnO NRAs underneath was clearly observed when organic photoactive layer was deposited from a low solution concentration. Meanwhile, the rougher surface also provides larger contact area between organic photoactive layer and metal contact, and thus leading to better charge collection efficiency [37, 38]. Even though better photovoltaic performance can be achieved by depositing a thinner organic photoactive film, the film must be thick enough to prevent the direct leakage current from ZnO NRAs to Ag electrode.

(a)

(b)

(c)

(d)

4. Conclusions

The effect of solution concentration of MEH-PPV and PCBM deposited onto Eosin-Y-coated ZnO NRAs on the performance of inverted-type organic solar cell has been investigated. The short circuit current density and power conversion efficiency greatly enhanced with decrease of solution concentration for both chlorobenzene- and chloroform-based devices, mainly due to reduce of charge recombination in thinner organic photoactive layer and larger contact area between the rougher organic photoactive layer and Ag contact. In contrast, the increase of leakage current from ZnO NRAs to Ag at lower solution concentration results in decrease of open circuit voltage. The highest power conversion efficiencies of 0.54 ± 0.10% and 0.87 ± 0.15% were achieved at the respective lowest solution concentration of CB and CF. It has been shown that the solution concentration played important role in improving performance of inverted-type organic solar cell.

Acknowledgments

This work has been carried out with the financial support of Malaysian Ministry of Science, Technology and Innovation (MOSTI) under Science Fund 03-01-02-SF0725. The authors would like to thank Mr. Idris Zulkifle from School of Applied Physics, Universiti Kebangsaan Malaysia for silver sputtering. The authors would also like to acknowledge Mr. Mohamad Hasnul Naim Abd Hamid and Mr. Muhammad Nazrul Zahari, both from Centre Research and Instrumentation Management (CRIM), Universiti Kebangsaan Malaysia, for FESEM and AFM characterizations, respectively.

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Copyright © 2013 Riski Titian Ginting et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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