Abstract
Carbon black (CB) and a 3D network epoxy polymer composite, representing dual functions for conductive corrosion protective layer (CCPL) and catalytic layer (CL) by the control of CB weight ratio against polymer is developed. Our strategy provides a proper approach which applies high catalytic ability and chemical stability of CB in corrosive triiodide/iodide (I3ā/Iā) redox electrolyte system. The CB and a 3D network epoxy polymer composite coated on the stainless steel (SS) electrode to alternate counter electrodes in dye sensitized solar cells (DSSCs). A two-step spray pyrolysis process is used to apply a solution containing epoxy monomers and a polyfunctional amine hardener with 6 wt% CB to a SS substrate, which forms a CCPL. Subsequently, an 86 wt% CB is applied to form a CL. The excellent catalytic properties and corrosion protective properties of the CB and 3D network epoxy polymer composites produce efficient counter electrodes that can replace fluorine-doped tin oxide (FTO) with CCPL/SS and Pt/FTO with CL/CCPL/SS in DSSCs. This approach provides a promising approach to the development of efficient, stable, and cheap solar cells, paving the way for large-scale commercialization.
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Introduction
For more than two decades, dye-sensitized solar cells (DSSCs) have been intensively investigated in industry and academia as a viable alternative to conventional silicon-based photovoltaic cells1,2,3,4,5,6,7,8,9,10. A typical DSSC comprises a dye-sensitized titanium dioxide (TiO2) nanocrystalline photoanode, an electrolyte that provided a redox couple (I3ā/Iā), and a counter electrode (CE)11. Significant research efforts have been applied toward optimizing each component by modifying the photoanodes, developing alternative dyes, improving the redox couple, and introducing structural changes, to yield highly efficient DSSCs12,13,14,15,16,17,18,19. Pt-coated fluorine-doped tin oxide (FTO) is typically used as the CE because of its excellent catalytic activity toward reducing I3ā. Unfortunately, Pt-coated CE is typically produced through high-temperature hydrolysis processes that are incompatible with flexible conducting polymer electrodes20,21,22,23,24. Furthermore, Pt corrodes in electrolytes containing iodide to generate PtI424,25,26. The Pt metal catalyst coating has been replaced with other materials, such as titanium nitrides 10,27, cobalt sulfide28, and carbon derivatives29,30,31,32,33. Carbon derivatives are particularly attractive, as they are abundant, low-cost, and provide high catalytic activities while remaining chemically stable in the presence of iodine redox couples32,33,34,35,36. Carbon black (CB) has been used on a large scale, for example in printing toners, reinforcing additives in automobile tires, and as conductive fillers in plastics, elastomers, and films37. CB is a conductive material with good catalytic activity for the reduction of triiodide38. Carbonaceous materials present active catalytic sites at their edges39. Therefore, CB, which have many edges, may be more active than highly structured carbon materials, such as graphites, graphenes, and carbon nanotubes40,41. CB powders cannot retain their shapes on a substrate; thus, they must be mixed with other binder materials, such as polymers or a TiO2 slurry containing organic surfactants and binders34,35,42. For example, GrƤtzel et al.40 and Jun et al.43, independently employed a CB/TiO2 slurry system in DSSC electrodes. Recently, Ho et al. reported the use of a CB/polymer composite CE comprising polypyrrole, polyaniline, or poly(3,4-ethylenedioxythiophene44. We, herein, extend the approaches introduced in these works by examining three-dimensional (3D) network polymers formed by polymerized monomers that had been cross-linked (XL) in-situ with CB to robustly fix the CB powders onto a substrate and act as a binder for the CB powders. The 3D network polymers are composed of an epoxy monomer and a polyfunctional amine hardener. The chemically XL epoxy polymer provides strong mechanical properties, chemical resistance, thermal resistance, and adhesive properties45,46.
Here, we describe the development of novel stainless steel (SS) CEs coated with a composite of CB and 3D networked polymers to replace conventional Pt CEs on FTO glass. Previous studies have reported the development of FTO glass alternates for the fabrication of flexible and bendable electrodes47,48. SSs are highly conductive and have a work function (ā4.4āeV) that is appropriate for use as a CE in DSSCs49. SSs are cost-effective materials compared with FTO glasses. Tan et al.50 and Kang et al.51 independently reported the development of an SS mesh and an SS substrate-based CE, respectively. However, the previous reports did not comment on the corrosion problems inherent to these materials and not show the long-term stability of the resulting DSSCs. Corrosion is a key technical feature that must be addressed in practical applications of SS CEs in DSSCs. In this work, we report a CB-coated SS CE with highly thermal stability, thus without corrosion problems. The photovoltaic performance for the device using this CB-coated SS CE remained nearly constant after 30 days of storage at 65āĀ°C. Meanwhile, a reference device consisting of Pt/FTO decreased up to almost 50% of the photovoltaic performance. We successfully coated both a conductive corrosion protective layer (CCPL) and a catalytic layer (CL) with a composite of CB and 3D network polymers onto an SS substrate using spray pyrolysis, as illustrated in Fig. 1a. The weights ratio of the CB incorporated into the polymer matrices of the CCPL and CL were 6 and 86wt%, respectively. The CCPL formed a compact dense structure that prevented corrosion due to electrolyte penetration, whereas the CL formed a nanoporous structure that provided a large surface area for increased catalytic activity.
Results
Percolation concentration of CB in CCPL
We optimized a coating composition containing CB and a polymer for use as a CCPL by preparing 4 samples (3, 6, 12, and 20 wt%), and we investigated their morphology, conductivity, corrosion protection properties, and electrical and catalytic properties. Figure 1b,c shows field emission scanning electron microscopy (FE-SEM) images of the CCPL layer cross-section and top surface, respectively. Smooth films with 2.4ā2.5āĪ¼m thick were obtained, and the CB are well-dispersed within the 3D XL polymer matrix.
The composites prepared with more than 6 wt% CB displayed well-established vertical interconnectivity among the CB due to the in-situ 3D XL polymer matrix, which appeared to improve as the CB content increase. The CB film did not detach from the composite during the pressure sensitive tape (PST) test. These results indicated that the XL polymers acted as an excellent binder for the CB. An efficient charge transport was obtained in the compact CB composites, and the in-situ generated 3D XL polymers guaranteed interconnections among the CB. Samples in which the CB were separated as a result of the large polymer content yield poor charge transport through the conducting CB network. Good mechanical properties, including adhesion, chemical resistance, and corrosion protection, were obtained at optimal composite compositions (e.g., at the percolation concentration) without incurring a loss in the conductivity52. The resistivities of the four composites using a 4-point probe method (see the inset in Fig. 2) were measured and the conductivities were calculated (Table 1).
The conductivity of the composite prepared 3 wt% CB was 0.081āS cmā1, almost one order of magnitude lower than the conductivity of a film prepared with 6 wt% CB (0.85āS cmā1). Further increases in the CB content only increased the conductivity to 0.96āS cmā1 at 20 wt% CB. Figure 2 shows the CB concentration-dependent conductivity. A critical point indicative of the percolation concentration was reached at 6 wt% CB. Therefore, we employed 6 wt% CB in the CCPL tested in this work.
Chemical resistance and corrosion protective properties of the CCPL
We next investigated the chemical resistance and corrosion protective properties of the CCPL (6 wt%) in the presence of an electrolyte solution and compared these properties to those obtained using a bare SS substrate dipped in an electrolyte containing 0.03āM iodine and additives (t-butyl pyridine (tBP) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI)) at 65āĀ°C. The bare SS substrate was completely corroded within a day, as indicated by the observed color change (Fig. 3a). On the other hand, no corrosion was observed at the CCPL surface, even after 30 days (Fig. 3b). We attempted to compare the bare SS surfaces before and after the soaking test by removing the CCPL layer, but the adhesion between the SS and CCPL layer was too robust to permit removal of the CCPL. These results demonstrated that the CCPL do not react with the electrolyte, and the CCPL effectively prevented the liquid electrolyte from reaching the SS. A 6 wt% CB solution provided the percolation concentration in our system which provided good adhesive properties, good chemical resistance and good corrosion protection ability without a loss in conductivity. In addition, the CCPL/SS electrode exhibited high flexibility due to the high ductility of a composite of CB and 3D network polymers on an SS substrate. Figure 3c shows no cracks under bending deformation of more than 100 times.
Redox activity of CCPL
Devices having a compact CCPL layer were firstly fabricated to evaluate the catalytic properties of the CCPL because the electrode (CCPL/SS) prepared with 6 wt% CB exhibited a reasonably high conductivity. In addition, we prepared a control CE based on a Pt-coated CCPL layer (Pt/CCPL/SS) for comparison with the CCPL/SS electrode. Figure 4a shows the JāV characteristics of the devices prepared with the CCPL/SS and Pt/CCPL/SS CEs. The devices employing the CCPL CE exhibited a very poor photovoltaic performance with a short-circuit current density (JSC) of 5.5āmA cmā2, an open-circuit voltage (VOC) of 0.53āV, a fill factor (FF) of 14.9%, and a power conversion efficiency (PCE) of 0.43%. These values were lower than those obtained from the device employing the Pt/CCPL/SS CE (JSCā=ā17.7āmA cmā2, VOCā=ā0.70āV, FFā=ā59.4%, and PCEā=ā7.3%). These results indicated that the compact CCPL CE could not function as both a corrosion protective layer and as a catalytic layer due to the insufficient contact area between the CB nanoparticles and I3ā. A good photovoltaic performance was obtained from the device prepared with the Pt/CCPL/SS CE, demonstrating that FTO can be replaced with a CCPL/SS substrate. These results suggested that the electron transport from the Pt layer to the SS through the interconnected CB in the CCPL was highly efficient. Figure 4b shows the electrochemical impedance spectroscopy (EIS) results of CCPL/SS and Pt/CCPL/SS CEs in symmetric cells consisting of two identical CEs (see Figure S1 for the equivalent circuit models). The impedance spectrum of the Pt/CCPL/SS CE was dominated by the I3ā/Iā redox reaction at Pt and the charges transfer to the SS through the CB in the CCPL. Assuming that the Pt/CB and CB/SS interfaces were characterized as non-Ohmic and Ohmic contacts, respectively, two different interfaces were expected to be present: the electrolyte/Pt and Pt/CB interfaces. Indeed, two semicircles were observed in the spectra. The small semicircle at high frequencies and the large semicircle at low frequencies (in the dark, under a forward bias) were attributed to electron transfer (series resistance, RSā=āca. 11āĪ©cm2) at the Pt/CB interface and the redox reaction (charge transfer resistance, RCTā=āca. 40āĪ©cm2) at the electrolyte/Pt interface, respectively. These results indicated that the catalytic activity of Pt is good, although electrons were more easily transport from Pt to the CB than from Pt to the electrolyte during catalysis. A symmetric cell consisting of two CCPL/SS CEs exhibited only one semicircle characterized by 10,500āĪ©cm2 at the electrolyte/CB interface due to the Ohmic contact at the CB/SS interface; however, the RCT value is large, indicating poor catalytic properties at the CCPL CE. This result agree well with the poor photovoltaic performances of the devices prepared with only the CCPL CE, suggesting that a catalytic layer (CL) with a nanoporous structure was required to increase the surface area at the electrolyte/CB interface.
Adhesive property of the CL
The CB content was increased (and the polymer content decreased) to increase the surface area of the CB. This could decrease the adhesion properties of the CB on the 3D XL polymer matrix. The maximum CB content at which the CB did not detach from the surface of the CL was identified by conducting a pull-off adhesion strength test using a PST to evaluate the adhesive properties of the CLs having CB contents up to 95 wt%. Figure S2 shows representative photographs of the pull-off adhesion strength test results obtained from the two CLs containing 86 or 90 wt% CB. The detachment of CB on the surfaces of the PST was not observed until an 86 wt% CB is used in the CLs. A greater number of CB were found to detach at concentrations beyond this threshold. The detached CB were clearly visible on the PST at and above a 90 wt% CB in the CL, as indicated by the yellow dotted circle in the photograph of the PST surface. These results were used to determine a CB concentration of 86 wt% in the optimized CL on the CCPL.
Electrochemical catalytic ability of the CL
In order to investigate the electrochemical catalytic abilities of the CL, cyclic voltammetry (CV) measurement was performed using a three-electrode electrochemical system with a scan rate of 30āmV/s. The working electrodes were CL/CCPL/SS electrodes with 40, 55 or 86 wt% CB in the CLs. Pt/FTO and CCPL/SS electrodes also tested for comparison. A Pt wire and Ag/AgCl were used as a counter electrode and a reference electrode, respectively, in the acetonitrile solution. As shown in Fig. 5a, each CV curve presents one pair of redox peaks corresponded to the reaction of I3āā+ā2eāāāā3Iā. An anodic peak current density (Jpa) and a cathodic peak current density (Jpc) corresponded to the oxidation of the iodide ions and the reduction of the tri-iodide ions, respectively. The oxidation/reduction peaks for the Pt/FTO electrode were shown at 0.352āV/ā0.210āV with peak to peak separation potential (Epp) of 0.562āV and Jpa/Jpc values were 1.211āmA cmā2/ā0.700āmA cmā2. The narrower Epp and higher Jp indicated better electrochemical catalytic ability. In the CCPL/SS electrode, very small amounts of currents flew through the surface of CCPL which had a compact dense structure with a small surface area. The small amounts of currents account for a high RCT value obtained from EIS measurement. CV results of electrodes with increased CB weight ratio (40, 55 or 86 wt%) in the CL presented decreased Epp and enlarged Jp values, indicating effective electrochemical catalytic abilities. The increase of weight ratio of CB in the CL resulted in a higher surface area, where redox reaction occurred, inducing the smaller RCT. The Epp, Jpa and Jpc values of the CL(86wt%)/CCPL/SS electrode were 0.576āV, 1.206āmA cmā2 and ā0.701āmA cmā2, respectively. This alternative electrode exhibited the efficient charge transfer ability, which was comparable with the Pt/FTO electrode by the decline of Rct. Figure 5b shows the Jpa and Jpc of the Pt/FTO electrode and the CL(86wt%)/CCPL/SS electrode during the 20 consecutive cycle scans. The Jp values of the CL/CCPL/SS electrode were almost maintained steadily, which revealed the excellent electrochemical stability in the I3ā/Iā based electrolyte system.
Photovoltaic performances and impedance analysis of DSSCs
As demonstrated above, the electrochemical impedance spectroscopy (EIS) measurements obtained from the symmetric cells established the criteria for the CL surface activity. Figure 5c shows the EIS spectra obtained from symmetric cells consisting of CL/CCPL/SS CEs with 40, 55 or 86 wt% CB in the CLs. One semicircle corresponded to Ohmic contact between the CB in the CL and the CCPL. The resistance of the CL (40 wt%) due to the catalytic activity at the electrolyte/CB interface was RCTā=ā119āĪ© cm2, much smaller than the resistance obtained from the CCPL (10,500āĪ© cm2 for 6 wt% CB). This value decreased as the CB concentration increase. RCT for the CB (86 wt%) is 41āĪ© cm2, almost equal to the value obtained from Pt/CCPL (40āĪ© cm2, Table 1).
Photocells employing CL/CCPL/SS CEs having 40, 55, or 86 wt% CB in the CLs were fabricated, and the J-V characteristics under simulated air mass 1.5 global (AM 1.5G) solar irradiation were measured. The photovoltaic parameters, measured resistance values and catalytic activities are summarized in Table 2, and the representative JāV characteristics are presented in Fig. 5d. The photovoltaic performances of the devices followed the trends in the RCT values, indicating that the catalytic activity at the electrolyte/CB interface could be enhanced by increasing the CB content in the CL of the CL/CCPL/SS CE. As the CB content in the CL increased, the FF values increased from 40.3 to 60.6% due to the enhanced catalytic activity, which minimized the recombination reaction between photoinduced electrons and I3ā. The improved catalytic activity affected the VOC values according to the equation: VOCā~ā(nkT/q)āĆāln(JSC/JS), where, n is the device ideality factor, k is the Boltzmann constant, T is the temperature in Kelvin, q is the fundamental charge, and JS is the saturation current density53,54.
The best performance was obtained from the device prepared with a CL(86 wt%)/CCPL/SS CE, yielding JSCā=ā14.9āmA cmā2, VOCā=ā0.68āV, FFā=ā60.6%, and PCEā=ā6.1%. With the exception of JSC, these values were equal to those obtained from a device prepared with a Pt/CCPL/SS CE (JSCā=ā17.7āmA cmā2, VOCā=ā0.70āV, FFā=ā59.4%, and PCEā=ā7.3%) as summarized in Table 1. In general, the JSC values could be estimated using the equation: JSCā=āqāĆāĪ·lhāĆāĪ·injāĆāĪ·ccāĆāIo, where q is the fundamental charge of an electron, Io is the intensity of the incident light, Ī·lh is the light harvesting efficiency, Ī·inj is the electron injection efficiency from the excited dye molecules to the TiO2 conduction band, and Ī·cc is the charge collection efficiency of the injected electrons at the transparent conductive oxide (TCO) layer. Assuming that Io, Ī·inj, and Ī·cc were equal in the two devices, different JSC values could account for the variations in the quantity of dye molecules adsorbed onto the electrodes, as reflected in Ī·lh, although we employed identical experimental conditions (Figure S3). The different counter electrodes in this study did not significantly affect the JSC values once a reasonably high FF had been achieved due to the effective catalytic properties.
We further compared the performance properties of the CL(86 wt%)/CCPL/SS CE with a conventional Pt/FTO CE. The device prepared with a Pt/FTO CE afforded JSCā=ā15.4āmA cmā2, VOCā=ā0.74āV, FFā=ā62.9%, and PCEā=ā7.1%). Interestingly, the VOC value was slightly larger than that (0.68āV) obtained from the CL(86 wt%)/CCPL/SS CE. As mentioned above, the VOC value might be sensitive to the JSC drop caused by the recombination reaction due to the relatively ineffective catalytic activity of the CL(86 wt%)/CCPL/SS CE compared to the Pt/FTO CE; however, the FF and JSC values of the CL(86 wt%)/CCPL/SS CE were similar to those measured in the Pt/FTO CE; thus, the small VOC value measured in the CL(86 wt%)/CCPL/SS CE could not be attributed to the JSC drop alone. The theoretical VOC could be calculated from the energy difference between the quasi-Fermi level of a nanocrystalline TiO2 working electrode under illumination and the redox potential of the I3ā/Iā pair in the electrolyte. The redox potential of the electrolyte (Eredox) is given by the Nernst equation: Eredoxā=āE0ā+ā(RT/2F)ln([I3ā]/[Iā]3), where E0 is the formal potential, R is the gas constant, T is the absolute temperature, and F is the Faraday constant. In addition to the JSC drop, the small VOC value obtained from the CL(86 wt%)/CCPL/SS CE may have accounted for the increased Eredox due to changes in the redox species concentration at the surface of the dye-sensitized TiO2 photoanode.
We previously observed that I3ā molecules became entrapped in the highly porous network polymer matrix at a TiO2 photoanode, thereby increasing VOC. Here, the opposite conditions were present because we employed a porous 3D network polymer matrix at the CE. These conditions were consistent with the measured decrease in VOC as the polymer content in the CLs increased, which increased the number of sites available to trap I3-. Nevertheless, the PCE of the device prepared with the CL(86 wt%)/CCPL/SS electrode reached a PCE that is 86% of the PCE obtained from a device prepared with Pt/FTO. Our results suggest that FTO could be replaced with CCPL/SS, but also that Pt/FTO could be replaced with CL/CCPL/SS.
In conclusion we successfully fabricated a novel flexible and cost-effective stainless steel (SS) counter electrode from a composite composed of CB and 3D network polymers to function as a CCPL and CL. The composite film, which provided a catalytic layer and acted as a conductive corrosion protective film, was prepared using a mixture of CB, cross-linkable epoxy monomers, and polyamine hardener and was applied using the spray pyrolysis method. The SS substrate acted as an efficient charge collecting electrode. The CCPL (6 wt% of CB) was chemically stable against electrolytes and successfully prevent the penetration of electrolytes, demonstrating excellent corrosion protective properties. The Pt/CCPL/SS CE was successfully substituted for a conventional Pt/FTO CE and displayed a photovoltaic performance (PCEā=ā7.3%) that was equivalent to that obtained from PT/FTO (PCEā=ā7.1%). The CL (86% of CB) provided an effective substitute for the conventional catalytic material (Pt). The DSSC prepared using the CL/CCPL/SS CE also displayed a high photovoltaic performance (PCEā=ā6.1%). We demonstrated that the CB-coated SS CE (CL/CCPL/SS CE) exhibited highly thermal stability, thus there were no corrosion problems. Furthermore, these results demonstrated that FTO can be replaced with CCPL/SS and Pt/FTO can be replaced with CL/CCPL/SS. Further performance enhancements may be realized by carefully optimizing the device architecture.
Methods
Chemicals and materials
Stainless steel (SS) was provided from POSCO. Carbon black (CB) powders purchased from Beilum Carbon Chemical Limited. Polyethylenimine (branched, average Mw ~25,000 by light scattering method, average Mn ~10,000 by GPC), trimethylolpropane triglycidyl ether, tert-butanol, iodine (I2), guanidinium thiocyanate (GuSCN), 4-tert-butylpyridine (tBP), acetonitrile (AN), and valeronitrile (VN) were purchased from Sigma-Aldrich. Fluorine-doped SnO2 (FTO) glass, Ti-nanoxide T/SP. Ti-nanoxide R/SP, cis-diisothiocyanato-bis(2,2ā²-bipyridyl-4,4ā²-dicarboxylato) ruthenium(II) bis(tetrabutyl-ammonium) (N719), 1-butyl-3-methylimidazolium iodide (BMII) were purchased from Solaronix SA. Spray gun (AIR BRUSH KIT, ABS-130) was purchased from Bluebird.
Preparation of the stainless steel counter electrode with a composite of CB and cross linked (XL) 3D network polymers
A SS substrate was cleaned using water and ethanol, then dried using air blow. The cleaned SS was placed onto the hotplate at 120āĀ°C. Trimethylolpropane triglycidyl ether and polyethylenimine was dissolved in ethanol. Various wt% (3, 6, 12, 20, 40, 55, 86 and 90 wt% ) of CB was dispersed in the solution through ultrasonication (750 W, Sonics & Materials, Inc, Newtown, CT, USA) for 10āmin. Firstly, the mixed solution with small wt% of CB to polymer was sprayed onto the SS substrate to form a CCPL. Subsequently, the mixed solution with large wt% of CB to polymer was sprayed onto the CCPL to form a CL. Each spray pyrolysis step was taken for 5āminutes in speed of 2āmL minā1. In-situ cross-linking network polymerization instantly occurred as soon as the mixed solution sprayed at the hot SS substrate or the hot CCPL.
Additional Information
How to cite this article: Kang, G. et al. Pt-Free Counter Electrodes with Carbon Black and 3D Network Epoxy Polymer Composites. Sci. Rep. 6, 22987; doi: 10.1038/srep22987 (2016).
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Acknowledgements
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (Code No. 2015R1A2A1A10054230) and the Center for Advanced Soft Electronics under the Global Frontier Research Program (Code No. NRF-2012M3A6A5055225) through the National Research Foundation of Korea (NRF) by the MSIP, Korea. Partial support for this work was provided by POSCO.
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T.P. and G.K. designed the study. G.K. executed the experiments. J.C. carried out the scanning electron microscope. T.P. and G.K. wrote the manuscript. All authors read and approved the final manuscript.
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Kang, G., Choi, J. & Park, T. Pt-Free Counter Electrodes with Carbon Black and 3D Network Epoxy Polymer Composites. Sci Rep 6, 22987 (2016). https://doi.org/10.1038/srep22987
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DOI: https://doi.org/10.1038/srep22987
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