<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">EPE</journal-id><journal-title-group><journal-title>Energy and Power Engineering</journal-title></journal-title-group><issn pub-type="epub">1949-243X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/epe.2012.46060</article-id><article-id pub-id-type="publisher-id">EPE-25075</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Engineering</subject></subj-group></article-categories><title-group><article-title>
 
 
  Fabrication and Characterization of Bulk Heterojunction Solar Cells Based on Liquid-Crystal Semiconductive Polymer
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>tsushi</surname><given-names>Suzuki</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Shinichi</surname><given-names>Ogahara</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tsuyoshi</surname><given-names>Akiyama</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Takeo</surname><given-names>Oku</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Materials Science, The University of Shiga Prefecture, Hikone, Japan</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>suzuki@mat.usp.ac.jp(TS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>22</day><month>11</month><year>2012</year></pub-date><volume>04</volume><issue>06</issue><fpage>459</fpage><lpage>464</lpage><history><date date-type="received"><day>September</day>	<month>14,</month>	<year>2012</year></date><date date-type="rev-recd"><day>October</day>	<month>15,</month>	<year>2012</year>	</date><date date-type="accepted"><day>October</day>	<month>30,</month>	<year>2012</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Bulk heterojunction solar cells based on poly poly(9,9-dioctylfluorene-co-bithiophene) (F8T2) as liquid crystal semiconductive polymer and C
  <sub>60</sub> as electron acceptor were fabricated and characterized. Thermal treatment of the bulk heterojunction films at annealing in the range of glass temperature and liquid crystal transition was performed for tuning optimization with improving the photovoltaic and optical properties. The photovoltaic performance was depended on morphological behavior in active layer at crystal state below glass temperature. The F8T2 thin film worked for electron-donor layer as p-type semiconductor to support charge transfer in active layer. Mechanisms of the photovoltaic properties were discussed on the basis of experimental results.
 
</p></abstract><kwd-group><kwd>Liquid Crystal Polymer; Bulk Heterojunction Solar Cell; Photovoltaic Property; Optical Property</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Organic solar cells have their unique advantages of useful applications, low cost, light weight and easy processing [1,2]. The organic solar cells based on a low band gap conjugated polymer and fullerene have been studied in recent years [3,4]. Advantages of liquid crystal semiconductive polymer have spontaneous self-assembly, relatively high charge mobility, easy deposition by spin coating, roll to roll or ink-jet printing. For instant, liquid crystal semi-conductor polymer of poly(9,9-dioctylfluoreneco-bithiophene) (F8T2) as a block copolymer with alternating dioctylfluorene and bithiophene segments have been applied as hole transporting layer, organic fieldeffect transistors and photovoltaic system [<xref ref-type="bibr" rid="scirp.25075-ref5">5</xref>]. The F8T2 copolymer with bithiophene segments affords good holetransporting properties [<xref ref-type="bibr" rid="scirp.25075-ref6">6</xref>]. The liquid crystal semiconductor polymer of F8T2 depending on thermal treatment has been applied electron devices with charge transfer based on molecular interaction of molecular self-coagulation [<xref ref-type="bibr" rid="scirp.25075-ref7">7</xref>].</p><p>Bulk heterojunction organic solar cell of F8T2 and fullerene as p-type and n-type semiconductors has been studied for improving photovoltaic and optical properties. A significant improvement of the photovoltaic performance has been reported by using bulk heterojunction thin film in the wide range of spectra. Weight ratio of composition in active layer has been varied to investigate relationship between morphological behavior and the photovoltaic properties [8,9]. Control of morphology of the bulk heterojunction film is important for tuning in optimizing exciton diffusion, charge separation, and electron (hole) transfer to cathode (anode). The photovoltaic properties have been an influence on molecular ordering in crystal phase controlled by heat treatment at glass temperature and liquid crystal transition. Crystallographic structure and morphological behavior of bithiophene-fluorene copolymer and fullerene varied with mole ratio of segment has been studied for improving the photovoltaic performance [9,10].</p><p>The purpose in this study is to fabricate and characterrize bulk heterojunction organic solar cell based on liquid crystal semiconductive polymer of F8T2 and fullerenes (C<sub>60</sub>) as electron donor and acceptor. Relationship between the photovoltaic properties and morphological behavior will be focused on tuning for optimization of photovoltaic performance. The thermal behavior on morphological behavior and molecular ordering of the liquid crystal polymer of F8T2 mixed with C<sub>60</sub> in the active layer will be investigated by polarized optical mi-croscopy, atomic force microscopy (AFM) and Raman scattering spectra. Mechanism of the photovoltaic and optical properties will be discussed on the basis of experimental results.</p></sec><sec id="s2"><title>2. Experimental</title><p>Poly(9,9-dioctylfluorenyl-2,7-diyl)-co-bithiophene (F8T2), poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) and C<sub>60</sub> were used as received from Aldrich Co. Ltd. and Material technologies Research. The molecular structure of C<sub>60</sub> and F8T2 were shown in Figures 1(a) and (b). The number and weight average molecular weight of F8T2 was M<sub>n</sub> &gt; 20,000 and M<sub>w</sub> = 41,126, as reported by Aldrich Co. Ltd. Mole ratio of (9,9-dioctylfluorenyl-2,7-diyl) and (bithiophene) element parts in F8T2 was 1 to 1, which indicates alternative copolymer. A repeat of cleaning ITO (A11DU80, AGC Fabritech Co. Ltd. 2 &#215; 2 cm, 10 Ω/sq.) was taken by organic solvents such as acetone, methanol and distilled water. The ITO substrate was dried by N<sub>2</sub> gas. The ITO substrate was irradiated with UV lamp for 30 minutes. PEDOT:PSS was spin-coated on the cleaned ITO substrate in glove box under N<sub>2</sub> atmosphere. Heat treatment was carried out at 100˚C for 20 min in N<sub>2</sub> atmosphere.</p><p>Bulk heterojunction films of F8T2 (10 mg) and C<sub>60</sub> (10 mg) solved in o-dichlobenzene (1.0 mL) was prepared on the PEDOT:PSS film based on the ITO substrate by spin coating (MIKASA SPINCOATOR 1H-D7). Heat treatment was carried out at several temperatures for 25 min. The substrate was cooled down in N<sub>2</sub> atmosphere. Aluminum (Al) metal was evaporated at thickness of about 100 nm in an area of 0.16 cm<sup>2</sup> on a top of the organic layer. <xref ref-type="fig" rid="fig1">Figure 1</xref>(c) shows schematic diagram of the bulk heterojunction solar cells of F8T2/C<sub>60</sub>.</p><p>Light and dark current density voltage (J-V) characteristics (Hokuto Denko Corp., HSV-110) of the solar cells mentioned above were measured under AM 1.5 (100 mW&#215;cm<sup>–</sup><sup>2</sup>) irradiation (Sanei Electric, XES-301S) in N<sub>2</sub> atmosphere. Optical properties of the heterojunction film were measured by UV-vis spectroscopy (Hitachi U-4100). Surface morphology of the active layer was observed by AFM (SII Nano Technology Inc. SII SPA400). Thermal behaviors of the F8T2 films were measured by DSC (PERKIN ELMER DSC Pyris 1). Raman scattering spectra were recorded with a Laser Raman Spectrometer (NRS-5100, JASCO Co., Ltd.). Raman mode and optical image of the active thin film after annealing at 70˚C was observed using excitation laser wavelength at 532 nm.</p><p>The molecular structure of F8T2 monomer was optimized by CS Chem3D (Cambridge Soft). Molecular orbital calculations were carried out by MOPAC (Fujitsu Ltd.). The isolated molecular structures were optimized by ab-initio quantum calculation using density functional theory using B3LYP/6-31G (d) as basis function (Gaussian 03). The electronic structures with energy levels at HOMO and LUMO were calculated. Active modes in Raman scattering spectra were calculated by DFT/ B3LYP/6-31G (d) using frequency mode.</p></sec><sec id="s3"><title>3. Results and Discussion</title><p>Thermal behaviors in the range of glass temperature and liquid crystal transition of the F8T2 polymer films were investigated as shown in <xref ref-type="fig" rid="fig2">Figure 2</xref>. Thermal transition for F8T2 was conformed to be at 118.5˚C, 267.5˚C and 305.5˚C, which were suitable for a glass temperature (T<sub>g</sub>), liquid-crystal transition and isotropic transition. These values were closed to be transition points, 128.5˚C, 259.3˚C, 314.1˚C, as reported in previous literature [<xref ref-type="bibr" rid="scirp.25075-ref5">5</xref>]. The annealing treatment at several temperatures was carried out for improving the photovoltaic properties and molecular ordering in active layer.</p><p>The photovoltaic performance including current voltage curves in the dark and illumination of the F8T2/C<sub>60</sub> bulk heterojunction solar cells were measured as shown in <xref ref-type="fig" rid="fig3">Figure 3</xref>. In the case of annealing condition at 70˚C below glass temperature, the light-induced J-V curves in the bulk heterojunction solar cell displayed a slight increase of photo-induced current density in dependence on applied voltage. The light-induced J-V curves of the solar cells indicated the photovoltaic behavior, which had a light induced rectification in strain diode characterization with exponential function of light induced current depending on applied voltage. The photovoltaic performance was improved by annealing treatment at 70˚C and 100˚C below glass temperature. However, the performance was reduced with arising annealing temperature at 130˚C and 190˚C below liquid crystal transition.</p><p><xref ref-type="table" rid="table1">Table 1</xref> shows measured parameters varied with the annealing condition. In the case of the photovoltaic characterization after annealing condition at 70˚C and 100˚C below the glass temperature, the measured parameters, open circuit voltage (V<sub>oc</sub>), short circuit current (J<sub>sc</sub>), fill factor (FF) and light conversion efficiency (η) were obtained to be 0.75 V, 0.55 mA&#215;cm<sup>–2</sup>, 0.16, 6.8 &#215; 10<sup>–2</sup>% for 70˚C, 0.37 V, 0.48 mA&#215;cm<sup>–2</sup>, 0.27 and 4.8 &#215; 10<sup>–2</sup>% for 100˚C, respectively. At 130˚C and 160˚C, the experimental results indicate a slight increase of photoinduced current density depending on the voltage, the measured parameters, V<sub>oc</sub>, J<sub>sc</sub> and FF were obtained to be 2.4 &#215; 10<sup>–2</sup> V, 5.3 &#215; 10<sup>–3</sup> mA&#215;cm<sup>–2</sup>, 0.15, for 130˚C and 0.48 V, 6.8 &#215; 10<sup>–3</sup> mA&#215;cm<sup>–2</sup>, 0.16 for 160˚C. The conversion efficiency, η was estimated to be 1.9 &#215; 10<sup>–5</sup>% and 5.4 &#215; 10<sup>–4</sup>%, respectively. In contrast case, device parameters for F8T2/C<sub>70</sub> bilayer were referred to be 0.76 V, 3.07 mA&#215;cm<sup>–2</sup>, 0.43 for 100˚C, 0.67 V, 9.55 mA&#215;cm<sup>–2</sup> and 0.53 for 200˚C [<xref ref-type="bibr" rid="scirp.25075-ref11">11</xref>]. The conversion efficiency, η was reported to be 1.2% and 3.4%, respectively. The photovoltaic performance for the F8T2/C<sub>70</sub> bilayer was origi-</p></sec></body><back><ref-list><title>References</title><ref id="scirp.25075-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">W. Chen, T. Xu, F. He, W. Wang, C. Wang, J. Strzalka, Y. Liu, J. Wen, D. J. Miller, J. Chen, K. Hong, L. Yu and S. B. Darling, “Hierarchical Nanomorphologies Promote Exciton Dissociation in Polymer/Fullerene Bulk Heterojunction Solar Cells,” Nano Letters, Vol. 11, No. 2, 2011, pp. 3707-3713. doi:10.1021/nl201715q</mixed-citation></ref><ref id="scirp.25075-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Y. Liang and L. Yu, “A New Class of Semiconducting Polymers for Bulk Heterojunction Solar Cells with Exceptionally High Performance,” Accounts of Chemical Research, Vol. 43, No. 9, 2010, pp. 1227-1236.  
doi:10.1021/ar1000296</mixed-citation></ref><ref id="scirp.25075-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">B. Carsten, J. M. Szarko, H. J. Son, W. Wang, L. Lu, F. He, B. S. Rolczynski, S. J. Lou, L. X. Chen and L. Yu, “Examining the Effect of the Dipole Moment on Charge Separation in Donor—Acceptor Polymers for Organic Photovoltaic Applications,” Journal of the American Chemical Society, Vol. 133, No. 50, 2011, pp. 20468-20475.  
doi:10.1021/ja208642b</mixed-citation></ref><ref id="scirp.25075-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">T. Oku, K. Nomura, A. Suzuki and K. Kikuchi, “Effect of Perylenetetracarboxylic Dianhydride Layer as a Hole Blocking Layer on Photovoltaic Performance of Poly-Vinyl- carbazole: C60 Bulk Heterojunction Thin Films,” Thin Solid Films, Vol. 520, No. 7, 2012, pp. 2545-2548.  
doi:10.1016/j.tsf.2011.10. 163 </mixed-citation></ref><ref id="scirp.25075-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">J. H. Huang, C. Y. Yang, Z. Y. Ho, D. Kekuda, M. C. Wu, F. C. Chien, P. Chen, C. W. Chu and K. C. Ho, “Annealing Effect of Polymer Bulk Heterojunction Solar Cells Based on Polyfluorene and Fullerene Blend,” Organic Electronics, Vol. 10, No. 1, 2009, pp. 27-33.  
doi:10.1016/j.orgel.2008.09.007</mixed-citation></ref><ref id="scirp.25075-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">P. A. Levermore, R. Jin, X. Wang, J. C. Mello and D. D. C. Bradley, “Organic Light-Emitting Diodes Based on Poly(9,9-dioctylfluorene-co-bithiophene) (F8T2),” Advanced Functional Materials, Vol. 19, No. 6, 2009, pp. 950- 957. doi:10.1002/adfm.200801260</mixed-citation></ref><ref id="scirp.25075-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">J.-H. Huang, C.-P. Lee, Z.-Y. Ho, D. Kekuda, C.-W. Chu and K.-C. Ho, “Enhanced Spectral Response in Polymer Bulk Heterojunction Solar Cells by Using Active Materials with Complementary Spectra,” Solar Energy Materials and Solar Cells, Vol. 94, No. 1, 2010, pp. 22-28.  
doi:10.1016/j.solmat.2009.02.019</mixed-citation></ref><ref id="scirp.25075-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">E. Lim, B.-J. Jung, M. Chikamatsu, R. Azumi, K. Yase, L.-M. Do and H.-K. Shim, “Synergistic Effect of Polymer and Oligomer Blends for Solution-Processable Organic Thin-Film Transistors,” Organic Electronics, Vol. 9, No. 6, 2008, pp. 952-958. doi:10.1016/j.orgel.2008.06.018</mixed-citation></ref><ref id="scirp.25075-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">O. Werzera, R. Resela, B. Chernevc, H. Plankc, M. M. Rothmanne, P. Strohriegle, G. Trimmelf, A. Rapalloh and W. Porzioh, “Crystallographic Structure and Morphology of Bithiophene-Fluorene Polymer Nanocrystals,” Polymer, Vol. 52, No. 15, 2011, pp. 3368-3373.  
doi:10.1016/j.polymer.2011.04.063</mixed-citation></ref><ref id="scirp.25075-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">K. Sagane, M. Shakutsui, T. Tsutsui and K. Fujita, “Polymer Field Effect Transistors of F8T2 Prepared by Evaporative Spray Deposition using Ultradilute Solution Technique,” Journal of Materials Science and Technology, Vol. 21, No. 2, 2008, pp. 193-196.  
doi:10.2494/photopolymer.21.193</mixed-citation></ref><ref id="scirp.25075-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">D. Kekuda, J.-H. Huang, K.-C. Ho and C.-W. Chu, “Modulation of Donor—Acceptor Interface through Thermal Treatment for Efficient Bilayer Organic Solar Cells,” Journal of Physical Chemistry C, Vol. 114, No. 6, 2010, pp. 2764-2768. doi:10.1021/jp910023d</mixed-citation></ref><ref id="scirp.25075-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">M. C. Gather and D. D. C. Bradley, “An Improved Optical Method for Determining the Order Parameter in Thin Oriented Molecular Films and Demonstration of a Highly Axial Dipole Moment for the Lowest Energy π–π* Optical Transition in Poly(9,9-dioctylfluorene-co-bithiophene),” Advanced Functional Materials, Vol. 17, No. 3, 2007, pp. 479-485. doi:10.1002/adfm.200600056</mixed-citation></ref><ref id="scirp.25075-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">H. Kuzmany, R. Pfeiffer, M. Hulman and C. Kramberger, “Raman Spectroscopy of Fullerenes and Fullerene-Nanotube Composites,” Philosophical Transactions of the Royal Society of London, Vol. 362, No. 1824, 2004, pp. 2375- 2406. </mixed-citation></ref></ref-list></back></article>