A study of stainless steel-based dye-sensitized solar cells and modules

Stainless steel (StSt) has been applied as substrate material for efficient, flexible, nanoporous TiO₂ dye-sensitized solar cells (DSSCs) with the aim of improving the photochemical properties of current plastic-based flexible DSSCs. DSSCs with a StSt substrate show almost equivalent properties in efficiency and convenience to cells with a F-doped tin oxide (FTO) glass substrate. Specifically, the metal substrate allows application of high-temperature sintering processes and shows high conductance even after sintering. Cells fabricated with the StSt substrates have been investigated as individual cells and as modules. A comparison between conventional DSSCs with a FTO glass substrate and flexible DSSCs with a StSt substrate is presented. In addition, Pt-coated electrodes, which can serve as window electrodes for StSt-based DSSCs, are fabricated via two different methods, i.e., chemical reduction and annealing, and compared.     

Optical properties of nano-structured dye-sensitized solar cells

Radiative transfer computations are carried out to describe the intrinsic and effective optical properties of light diffusing and absorbing materials consisting of anatase titania pigments hosted in an electrolyte medium. The intrinsic visible absorption of some of the pigments has been increased by coating them with an absorbing dye monolayer. A multiple scattering approach is applied to compute average path-length parameters and forward-scattering ratios used in four-flux radiative transfer calculations. It is shown that the effective absorption coefficient of the inhomogeneous medium is maximized when the size of the pigments is around 12 nm in diameter, and the effective scattering coefficient is optimized for diameters of the pigments around 250 nm. The intrinsic solar absorptance of the medium is optimized when the diameter of the pigments is around 60 nm.     

Impedance characterization of dye-sensitized solar cells in a tandem arrangement for hydrogen production by water splitting

The present work reports the photoelectrochemical characterization of a dye-sensitized solar cell (DSC) to assist water split in a photoelectrochemical (PEC) cell. Performance parameters were extracted from standard current–voltage characteristic (I–V) and the charge transfer phenomena occurring at different interfaces of the DSC were evaluated by electrochemical impedance spectroscopy (EIS). The DSC comprised the N719 dye and a robust electrolyte (1-propyl-3-methylimidazolium iodide in guanidinium thiocyanate additive). At 1 sun illumination the DSC yielded a short-circuit photocurrent density of 14.9 mA cm⁻², an open-circuit voltage of 0.797 V, a fill factor of 0.712 and an overall efficiency of 8.5%. Different PEC systems based on silicon-doped and undoped hematite photoelectrodes were considered. The required additional anodic bias necessary for actual water cleavage was supplied by two DSCs in series operating just under open-circuit voltage (1.56 V), allowing a conversion efficiency of about 1.12% for the silicon-doped hematite deposited by APCVD, 0.51% for the silicon-doped prepared by USP and 0.12% for the undoped hematite sample.     

Faradaic impedance of dye-sensitized solar cells

Theoretical equations of the Faradaic impedance of the photoelectrode and the counter electrode of dye-sensitized solar cell (DSC) were derived. The Faradaic impedance is the frequency dependent resistance related to the time constants of elementary electrode processes like photoexcitation, electron transfer, charge transfer reaction and diffusion. The typical cell impedance spectrum describes the locus of three semicircles on the Nyquist plane. The locus of three semicircles is generally analyzed by using the equivalent circuit composed of charge transfer resistance (R_ct,1) and capacitance (C_dl,1) of counter electrode, charge transfer resistance (R_ct,2) and capacitance (C_dl,2) of photoelectrode, the finite diffusion impedance due to the diffusion of I₃⁻ on the counter electrode (Z_w), and total resistance of the substrate and solution (R_s). The physical meanings of R_ct,1 and R_ct,2 can be elucidated by the interpretations of Faradaic impedance derived in the present paper. The R_ct,1 is represented as the function of the potential-dependent rate constants of I₃⁻ reduction and I⁻ oxidation. On the other hand, the R_ct,2 is the function of the photoelectrode potential, the surface concentration of I₃⁻ and the potential-independent rate constant of the back electron transfer reaction. The theoretical expressions of the current-voltage (I-V) curve of the DSC can be also derived. In the present paper, the relations between the impedance and I-V curve of the DSC are discussed.     

Utilization of natural carotenoids as photosensitizers for dye-sensitized solar cells

The dye-sensitized solar cells (DSCs) were assembled by using natural carotenoids, crocetin (8,8′-diapocarotenedioic acid) and crocin (crocetin-di-gentiobioside), as sensitizers and their photoelectrochemical properties were investigated taking a presence or absence of carboxylic group in the dye molecule into consideration. In these carotenoids, crocetin that has carboxylic groups in the molecule can attach effectively to the surface of TiO₂ film so that it performed the best photosensitized effect resulting in the short-circuit photocurrent with 2.84 mA under irradiation of 1.0 cm². On the other hand, crocin that has no carboxylic group in the molecule showed lower photoelectrochemical performance because of its lower affinity to the surface of TiO₂ film. These results indicate that it is possible to apply carotenoid as sensitizers for DSCs at the presence of effective function groups.     

Influence of the organic electrolyte and anodization conditions on the preparation of well-aligned TiO2 nanotube arrays in dye-sensitized solar cells

Dye-sensitized solar cells (DSSCs) comprising randomly networked titanium nanoparticles usually exhibit lower energy conversion efficiency and limited electron mobility due to the scattering and trapping of free electrons. In this study, attempts were made to improve the electron mobility in DSSCs using vertically aligned and well ordered TiO₂ nanotubes. These nanotubes were prepared by the electrochemical etching of Ti foil under potentiostatic conditions in four different fluorinated organic solvents under varying anodizing conditions like reaction time, and annealing before/after anodization. Sonoelectrochemistry was found to be more effective to synthesize well-ordered TiO₂ nanotubes than just stirring the electrolyte as in conventional electrochemistry. Using NH₄F-EG as an anodizing electrolyte, unique TiO₂ nanomorphology with longer nanotubes length of 18 μm was achieved. The photo-electrochemical properties of the DSSCs with back illumination under UV (<400 nm) and simulated sunlight (AM 1.5) were also studied, and exhibited an efficiency of 2.13%. The results are reported in detail here.     

An inexpensive and efficient pyridine-based additive for the electrolyte of dye-sensitized solar cells

We report on the synthesis and application of an inexpensive pyridine-based additive allyl isonicotinate (AIN) for the efficient dye-sensitized solar cells (DSCs). AIN can be quickly synthesized at room temperature without any solvent. The presence of AIN in the electrolyte enhances the open-circuit voltage (V_oc), fill factor (FF) and short-circuit photocurrent (J_sc), consequently improving the energy conversion efficiency (η) from 6.5% to 8.2%. The impedance experiments show that the adsorption of AIN leads to the negative shift of the conduction band edge of the dye-sensitized TiO₂ around 55 mV. The presence of AIN in the electrolyte can obviously suppress the recombination of the injected electrons, increasing the lifetime of electrons in the TiO₂. The negative shift of the conduction band edge and the suppression of the recombination of the injected electrons contribute to the higher power conversion efficiency.     

Identification of PV solar cells and modules parameters using the genetic algorithms: Application to maximum power extraction

In this paper, we propose to perform a numerical technique based on genetic algorithms (GAs) to identify the electrical parameters (I_s, I_ph, R_s, R_sh, and n) of photovoltaic (PV) solar cells and modules. These parameters were used to determine the corresponding maximum power point (MPP) from the illuminated current-voltage (I-V) characteristic. The one diode type approach is used to model the AM1.5 I-V characteristic of the solar cell. To extract electrical parameters, the approach is formulated as a non convex optimization problem. The GAs approach was used as a numerical technique in order to overcome problems involved in the local minima in the case of non convex optimization criteria. Compared to other methods, we find that the GAs is a very efficient technique to estimate the electrical parameters of PV solar cells and modules. Indeed, the race of the algorithm stopped after five generations in the case of PV solar cells and seven generations in the case of PV modules. The identified parameters are then used to extract the maximum power working points for both cell and module.     

Application of mesoporous carbon to counter electrode for dye-sensitized solar cells

The mesoporous carbons were prepared by the carbonation of the triblock copolymer F127/phloroglucinol-formaldehyde composite self-assembled in an acid medium and employed as the catalyst for triiodide reduction in dye-sensitized solar cells (DSCs). The characteristics of mesoporous carbon were analyzed by scanning electron microscopy, transmission electron microscopy, N₂ sorption measurement and X-ray diffraction. The mesoporous carbon with low crystallinity exhibited Brunauer-Emmett-Teller surface area of 400 m² g⁻¹, pore diameter of 6.8 nm and pore volume of 0.63 cm³ g⁻¹. The photovoltaic performances of DSCs with mesoporous carbon counter electrode were improved by increasing the carbon loading on counter electrode due to the charge-transfer resistance of mesoporous carbon counter electrode decreasing with the increase of the carbon loading. However, further carbon loading increase has no obvious effect on the photovoltaic performance of DSCs with carbon electrode when carbon loading exceeds 300 μg cm⁻². The overall conversion efficiency of 6.18% was obtained by DSCs composed of mesoporous carbon counter electrode with the carbon loading of 339 μg cm⁻². This value is comparable to that of DSCs with conventional platinum counter electrode.     

A novel UV-mediated low-temperature sintering of TiO2 for dye-sensitized solar cells

Titania pastes were fired at 450 °C in oxygen to give white titania that was used to prepare dye-sensitized solar cells (DSSC). Titania fired at lower temperature and/or under inert atmosphere have brown stripes and cells made from these stripes had no measurable efficiency. When the titania paste was screen printed and then heated and simultaneously irradiated with UV light, white stripes were obtained. Improved efficiency was noted for PV cells made from pastes heated at lower temperature under irradiation vs. cells made from low-temperature heated paste but without irradiation. UV irradiation appears to facilitate clean oxidation of residual organic materials in the titania precursor pastes. The best cells in our study made with our titania paste treated at 450 °C in oxygen had the following characteristics: efficiency=3.45%; V_oc=630 mV; J_sc=8.5 mA/cm²; and a fill factor=0.64.     

Fabrication and characterization of dye-sensitized solar cells from rutile nanofibers and nanorods

Rutile titania (TiO₂) nanofibers were prepared by electrospinning a polymeric sol containing a titanium precursor and Poly(vinylpyrrolidone) in acetic acid-ethanol mixture and subsequent sintering of the fibers at 800 °C. The resultant continuous, polycrystalline porous fibers contained TiO₂ grains of 15-20 nm sizes. The continuous fibers were broken down into nanorods by mechanical grinding. Morphology of the nanofibers and nanorods was characterized by scanning and transmission electron microscopies. The crystal structure and polycrystallinity of the fibers were further confirmed by X-ray diffraction analysis. Dye-sensitized solar cells (DSCs) fabricated from the nanofibers and rutile nanorods, respectively, showed superior performance with the later.     

Novel iminocoumarin dyes as photosensitizers for dye-sensitized solar cell

Novel iminocoumarin dyes (2a-c and 3a-c) having carboxyl and hydroxyl anchoring groups onto the dyes skeletons have been designed and synthesized for the application of dye-sensitized nanocrystalline TiO₂ solar cells (DSSCs). The photophysical and electrochemical studies showed that these iminocoumarin dyes are suitable as light harvesting sensitizers in DSSC application. The dyes having carboxyl and hydroxyl anchoring groups (2a-c) showed better efficiency when compared to the dyes having carboxyl group (3a-c) alone. The cell consisted of dye 2a generated the highest solar-to-electricity conversion efficiency (η) of 0.767% (open circuit voltage (V_oc) = 0.491 V, short circuit photocurrent density (J_sc) = 2.461 mA cm⁻², fill factor (ff) = 0.635) under simulated AM 1.5 irradiation (1000 W m⁻²) with a total semiconductor area of 0.25 cm². The corresponding incident photon-to-current conversion efficiency (IPCE) of the above cell was 21.38%. The overall low efficiency of the dyes is ascribed to the lack of light harvesting ability at longer wavelength region.     

2-Ethyl-1-hexanol based screen-printed titania thin films for dye-sensitized solar cells

Nanocrystalline titania thin films were prepared by screen printing in order to efficiently control and optimize the main step of the dye-sensitized solar cells (DSSCs) fabrication process. Different compositions of nanocrystalline titanium dioxide screen-printing pastes are described, based on 2-ethyl-1-hexanol solvent and commercial Degussa P25 TiO₂. The rheological properties of the prepared pastes are presented as the crucial parameter of the deposition procedure. The produced titania thin films are extensively characterized by means of spectroscopy (Raman, XRD) and microscopy (SEM, AFM). The performance (induced photon-to-current efficiency—IPCE% and overall energy conversion efficiency—η%) of the corresponding DSSCs is also reported.     

On the photophysical and electrochemical studies of dye-sensitized solar cells with the new dye CYC-B1

In this study, the photoelectrochemical characteristics of a ruthenium photosensitizer with an alkyl bithiophene group, designated as CYC-B1, are studied. The effect of mesoporous TiO₂ film thickness on the photovoltaic performance of CYC-B1 and N3 dye-sensitized solar cells was investigated. The performance of the dye-sensitized nanocrystalline TiO₂ solar cells (DSSC) fabricated using CYC-B1 dye-anchored TiO₂ photoelectrode showed a convincing enhancement in cell efficiency when the TiO₂ film thickness was increased from 3 μm (eff.=5.41%) to 6 μm (eff.=7.19%). The efficiency of the CYC-B1-sensitized DSSC was maximum at 6 μm of the TiO₂ film thickness, reached its limiting value and remained constant up to 53 μm, although a similar trend was also observed for N3 dye-sensitized DSSC, however, the maximum efficiency achieved was only at 27 μm thickness (eff.=6.75%). As expected, the photocurrent density generated in the DSSC modified by CYC-B1 dye is larger than that from N3 dye. The effect of guanidinium thiocyanate (GuSCN) (additive) addition to the electrolyte on the photovoltaic performance of DSSCs based on CYC-B1 was also investigated. Furthermore, the electrochemical impedance spectroscopy (EIS) technique and photo-transient laser method have been employed to analyze the charge transfer resistances (R_ct) and the lifetime of the injected electrons on the TiO₂ containing different thicknesses.     

Improvement in long-term stability of dye-sensitized solar cell for outdoor use

To improve the intrinsic stability of the component of dye-sensitized solar cells (DSCs), we have fabricated the unit cell using solvent-free ionic liquid electrolyte. The degradation in the continuous 1 sun light soaking test at 60 °C over 15,000 h was effectively suppressed, compared with the cell using γ-butyrolactone electrolyte. The lifetime for outdoor use was estimated over 15 years from acceleration factor based on the outdoor exposure test. To confirm the stability of the DSC under practical outdoor use, we fabricated the solar light using the DSC modules, rechargeable batteries and bright light emitting diode (LED). The solar lights have been emitting a bright white light at night using the electricity from batteries charged by the DSC modules during the daytime in any weather condition for a half year.     

Europium complex doped luminescent solar concentrators with extended absorption range from UV to visible region

In this paper, a europium complex, Eu(TTA)₃Dpbt (TTA = thenoyltrifluoroacetonate, Dpbt = 2-(N,N-diethylanilin-4-yl)-4,6-bis(3,5-dimethylpyrazol-1-yl)-1,3,5-triazine), with extended absorption range is incorporated into polyvinyl-butyral (PVB) to fabricate luminescent solar concentrators (LSCs) on the face of K9 glass. This kind of LSC can absorb the light in the UV and the blue region and is free of self-absorption. External quantum efficiency of the LSC is measured at different wavelength. Under a solar simulator (AM1.5G), efficiency of Eu(TTA)₃Dpbt doped LSC is 11% higher than that of Eu(TTA)₃Phen doped LSC (0.176%), resulting from the absorption of Eu(TTA)₃Phen which is limited within UV region. It can be seen from this result that extending absorption region of lanthanide complexes can be used to further enhance efficiency of lanthanide complex doped LSC, besides these complexes are without self-absorption because of their large Stokes shift.     

Syntheses and photovoltaic properties of polymeric sensitizers using thiophene-based copolymer derivatives for dye-sensitized solar cells

We synthesized the thiophene-based copolymers (P(3TAF-co-3TAa)-A-n and P(3TAF-co-3TAa)-B-n) using two different kinds of thiophene monomers, (N-(3-thienylmethylene)-2-aminofluorene and 3-thiophene acetic acid), as sensitizers on the DSSCs. P(3TAF-co-3TAa)-A-n (n=1, 2, 3) was synthesized with different molar ratios (3TAF:3TAa=1:5, 1:10, 1:20) of monomers at room temperature, respectively. Also, P(3TAF-co-3TAa)-B-n (n=1, 2, 3) was synthesized with above molar ratios of monomers at 0 °C, respectively. The DSSCs devices were fabricated using the thiophene-based copolymers as sensitizers and their photovoltaic performances were measured by using a solar simulator under AM 1.5. In the DSSCs devices using polymeric sensitizers, V_oc is 0.53-0.60 V, J_sc is 1.9-4.5 mA/cm², FF is 0.51-0.63 and the power conversion efficiency is 0.63-1.53%, respectively.     

Influences of water in bis-benzimidazole-derivative electrolyte additives to the degradation of the dye-sensitized solar cells

The chemical stability of dye-sensitized solar cells (DSSC) determines both the cell performance and the cell life-time. The presence of water in the solar cell from surrounding leakage through the imperfection packaging sealants causes the decrease in life-time of photogenerated electrons on the working electrodes, which induces the occurrence of the dark current to the electrolytes and thus leakage current significantly deteriorated the life-time of the DSSC. Reliable electrolyte additives diminishing the influences of water to the DSSCs degradation process becomes a critical issue in maintaining an acceptable cell life-time.In this work, the effects of four benzimidazole derivatives a-d as the electrolyte additives in the presence of water were comprehensively examined by time-dependent photovoltaic performance of the cells. As a result, open-circuit voltage (V_oc), short-circuit current (J_sc), efficiency (η), and fill factor (FF) collected from I-V curves were studied. In addition, electrochemical impedance spectroscopy (EIS) technique was implemented to evaluate the effects of the charge-transfer resistance (R_ct) at the interfaces between TiO₂/dye/electrolyte. Results showed that the bis-benzimidazole derivative c gives significant improvement in the long-term stability due to the effective protection of the ligands between dye and working electrodes from the attack by environmental water molecules.     

On the use of triethylamine hydroiodide as a supporting electrolyte in dye-sensitized solar cells

For the first time, the application of a molten salt, triethylamine hydroiodide (THI), as a supporting electrolyte was investigated for the dye-sensitized solar cells (DSSCs). Titanium dioxide (TiO₂) electrode was modified by incorporation of high- and low-molecular weight poly(ethylene glycol) along with TiO₂ nanoparticles of two different sizes (300 nm (30 wt%) and 20 nm (70 wt%)). The highest apparent diffusion coefficient (D) of 8.12×10⁻⁶ cm² s⁻¹ was obtained for I⁻ (0.5 M of THI) from linear sweep voltammetry (LSV). Short-circuit current density (J_sc) increases with the concentration of THI whereas open-circuit potential (V_oc) remains the same. Optimum J_sc (19.28 mA cm⁻²) and V_oc (0.7 V) with a highest conversion efficiency (η) of 8.45% were obtained for the DSSC containing 0.5 M of THI/0.05 M I₂/0.5 M TBP in CH₃CN. It is also observed that the J_sc and η of the DSSC mainly relates with the D values of I⁻ and charge-transfer resistances such as R_ct1 and R_ct2 operating along Pt/TiO₂ electrolyte interface, obtained from LSV and electrochemical impedance spectroscopy (EIS). For comparison, tetraethylammonium iodide (TEAI) and LiI were also selected as supporting electrolytes. Though both the THI and TEAI have similar structures, replacement of one methyl group by hydrogen improves the efficiency of the DSSC containing the former electrolyte. Further, the DSSC containing THI exhibits higher J_sc and η than LiI (7.70%), from which it is concluded that THI may be used as an efficient and alternative candidate to replace LiI in the current research of DSSCs.     

Enhancing the performance of dye-sensitized solar cells by incorporating nanosilicate platelets in gel electrolyte

Two kinds of gel-type dye-sensitized solar cells (DSSCs), composed of two types of electrolytes, were constructed and the respective cell performance was evaluated in this study. One electrolyte, TEOS-Triton X-100 gel, was based on a hybrid organic/inorganic gel electrolyte made by the sol–gel method and the other was based on poly(vinyidene fluoride-co-hexafluoro propylene) (PVDF-HFP) copolymer. TEOS-Triton X-100 gel was based on the reticulate structure of silica, formed by hydrolysis, and condensation of tetraethoxysilane (TEOS), while its organic subphase was a mixture of surfactant (Triton X-100) and ionic liquid electrolytes. Both DSSC gel-type electrolytes were composed of iodine, 1-propy-3-methyl-imidazolium iodide, and 3-methoxypropionitrile to create the redox couple of I₃⁻/I⁻. Based on the results obtained from the I–V characteristics, it was found that the optimal iodine concentrations for the TEOS-Triton X-100 gel electrolyte and PVDF-HFP gel electrolyte are 0.05 M and 0.1 M, respectively. Although the increase in the iodine concentration could enhance the short-circuit current density (J_SC), a further increase in the iodine concentration would reduce the J_SC due to increased dark current. Therefore, the concentration of I₂ is a significant factor in determining the performance of DSSCs.In order to enhance cell performance, the addition of nanosilicate platelets (NSPs) in the above-mentioned gel electrolytes was investigated. By incorporating NSP-Triton X-100 into the electrolytes, the J_SC of the cells increased due to the decrease of diffusion resistance, while the open circuit voltage (V_OC) remained almost the same. As the loading of the NSP-Triton X-100 in the TEOS-Triton X-100 gel electrolyte increased to 0.5 wt%, the J_SC and the conversion efficiency increased from 8.5 to 12 mA/cm² and from 3.6% to 4.7%, respectively. However, the J_SC decreased as the loading of NSP-Triton X-100 exceeded 0.5 wt%. At higher NSP-Triton X-100 loading, NSPs acted as a barrier interface between the electrolyte and the dye molecules, hindering electron transfer, hence, reducing the cell's photocurrent density. The same behavior was also observed in the PVDF-HFP gel electrolyte DSSC system.