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Funding Information: The authors thank Jaakko Eskola for the photography of the coloured knits ( Fig. 23 ). This work was supported by Business Finland [Project Sun-powered Textiles, 3666/31/2019 ]. Publisher Copyright: © 2023 Integrating solar cells in textiles offers a promising path toward energy-autonomous wearable electronics, but their design requires careful optimisation between energy efficiency and visual aesthetics. For this purpose, we present a systematic study of the optical properties of knitted textiles as visually concealing covers for textile-integrated solar cells. The study investigates microscopic and macroscopic factors that influence the optical performance of knitted textiles. A set of 175 samples was knitted, including 20 knit structures, 6 yarn materials, and 20 yarn colours. The knitted samples were studied using optical characterisation methods such as spectroscopy, microscopy, and photography. We developed metrics characterising solar cell performance and visual appearance, which can be used to optimise textiles based on desired performance characteristics. The strong correlation between the performance metrics demonstrates a design compromise between solar cell performance and concealment. By applying aproposed set of optimisation criteria to the knitted samples, 23 out of the 175 samples qualified as the best in solar cell performance and concealment. The developed metrics are also applicable to other textile configurations and light-sensing applications.

The colorimetric and photovoltaic efficiency of different structural color coatings, including cellulose nanocrystals, were compared with spectrophotometry, photography, and power loss analysis in view of their application in solar architecture.

The daily Sun supplies the continents of the Earth with four times more energy than humanity consumes in a year. This enormous potential of solar energy to generate clean energy is therefore driving great efforts to replace conventional and unsustainable fossil fuel consumption that damages our climate and our environment. Solar photovoltaic (PV) is emerging as the fastest growing renewable energy technology in the world, yet its share to the electricity production currently is less than 3%. While coal and gas remain key to electricity production, the climate crisis demands a fast transition to a carbon-neutral energy system. In the year 2019, the PV industry produced solar panels with a capacity of about 115 GW. To reach multi-TW levels by 2030, PV production capacity needs to scale at high rates, and continued innovation is necessary. One way to increase production is to reduce silicon wafer thickness, making more cells from the amount of silicon produced. Thinning the cell will not only allow making more of them in less time but will also reduce the cost for a module, and for the electricity it generates. A thinner absorber reduces the absorption of sunlight. To counter this loss, optical concepts are needed. In this chapter, we review the most promising approaches in photonics that have made physically thinner but optically thicker solar cells possible. By enabling thinner solar cells, photonic solutions offer the possibility of efficiency enhancements at lower costs. We will explain their applications, discuss their challenges and estimate their impact on energy yield. Finally, we outline how non-silicon thin-film PV is opening up a plethora of consumer-oriented applications. Since the higher flexibility/bendability of thinner cells broadens their applicability range, thin-film PV will empower our transition to a 100% green society in many aspects of our lives.

Dye-sensitized solar cells (DSSCs) are an efficient photovoltaic technology for powering electronic applications such as wireless sensors with indoor light. Their low cost and abundant materials, as well as their capability to be manufactured as thin and light-weight flexible solar modules highlight their potential for economic indoor photovoltaics. However, their fabrication methods must be scaled to industrial manufacturing with high photovoltaic efficiency and performance stability under typical indoor conditions. This paper reviews the recent progress in DSSC research towards this goal through the development of new device structures, alternative redox shuttles, solid-state hole conductors, TiO2 photoelectrodes, catalyst materials, and sealing techniques. We discuss how each functional component of a DSSC has been improved with these new materials and fabrication techniques. In addition, we propose a scalable cell fabrication process that integrates these developments to a new monolithic cell design based on several features including inkjet and screen printing of the dye, a solid state hole conductor, PEDOT contact, compact TiO2, mesoporous TiO2, carbon nanotubes counter electrode, epoxy encapsulation layers and silver conductors. Finally, we discuss the need to design new stability testing protocols to assess the probable deployment of DSSCs in portable electronics and internet-of-things devices., Dye-sensitized solar cells (DSSCs) are an efficient photovoltaic technology for powering electronic applications such as wireless sensors with indoor light.

Although single-wall carbon nanotubes (SWCNTs) exhibit various colors in suspension, directly synthesized SWCNT films usually appear black. Recently, a unique one-step method for directly fabricating green and brown films has been developed. Such remarkable progress, however, has brought up several new questions. The coloration mechanism, potentially achievable colors, and color controllability of SWCNTs are unknown. Here, a quantitative model is reported that can predict the specific colors of SWCNT films and unambiguously identify the coloration mechanism. Using this model, colors of 466 different SWCNT species are calculated, which reveals a broad spectrum of potentially achievable colors of SWCNTs. The calculated colors are in excellent agreement with existing experimental data. Furthermore, the theory predicts the existence of many brilliantly colored SWCNT films, which are experimentally expected. This study shows that SWCNTs as a form of pure carbon, can display a full spectrum of vivid colors, which is expected to complement the general understanding of carbon materials.

Theoretical modeling of the incidence angle dependence is important for the performance evaluation of solar cells especially when they employ structural photonics that enhance their aesthetics for building-integrated photovoltaic applications. We present an optical model based on transfer matrix method, which is tailored for the analysis of the angular optical characteristics of dye-sensitized solar cells (DSSC) that incorporate a porous one-dimensional photonic-crystal (1DPC) back reflector. We provide complete mathematical description of the angular optics and electromagnetic energetics of DSSC, including solutions that avoid numerical instabilities in the case of thick, strongly light-absorbing layers. The model showed excellent quantitative agreement with angle-dependent spectral transmittance measurements recorded from complete DSSCs, allowing detailed analysis of the light harvesting enhancement by the dye provided by back-reflection of light from the 1DPC. Determining the ratio of the device transmittance measured with and without a 1DPC is proposed as a simple and practical way o determine the internal reflectance of the 1DPC embedded in the device structure. The reported model provides an accurate description of the coherent angular optics of DSSCs, applicable for situations where light scattering in the device structure can be neglected.

The success of perovskite and dye-sensitized solar cells will depend on their stability over the whole life-time. Aging tests are of utmost importance to identify deficiencies and to suggest cell improvements. Here we analyzed the quality of 261 recent aging tests and found serious shortcomings in current practices. For example, in about 50% of the studies only one sample was considered, meaning that the sample size was too small for statistical significance. We propose a new procedure for aging tests based on careful planning and scientific reporting. This includes estimating the required sample size for an aging test and avoiding so-called nuisance factors, i.e. unintended variations always present in real world testing. The improved procedure can provide more reliable information on stability and lifetime, which could contribute to better understanding of degradation mechanisms important for improving these photovoltaic technologies.

A comparative analysis of perovskite structured cathode materials, La0.65Sr0.35MnO3 (LSM), La0.8Sr0.2CoO3 (LSC), La0.6Sr0.4FeO3 (LSF) and La0.6Sr0.4Co0.2Fe0.8O3 (LSCF), was performed for a ceramic-carbonate nanocomposite fuel cell using composite electrolyte consisting of Gd0.1Ce0.9O1.95 (GDC) and a eutectic mixture of Na2CO3 and Li2CO3. The compatibility of these nanocomposite electrode powder materials was investigated under air, CO2 and air/CO2 atmospheres at 550 °C. Microscopy measurements together with energy dispersive X-ray spectroscopy (EDS) elementary analysis revealed few spots with higher counts of manganese relative to lanthanum and strontium under pure CO2 atmosphere. Furthermore, electrochemical impedance (EIS) analysis showed that LSC had the lowest resistance to oxygen reduction reaction (ORR) (14.12 Ω∙cm2) followed by LSF (15.23 Ω∙cm2), LSCF (19.38 Ω∙cm2) and LSM (>300 Ω∙cm2). In addition, low frequency EIS measurements (down to 50 μHz) revealed two additional semi-circles at frequencies around 1 Hz. These semicircles can yield additional information about electrochemical reactions in the device. Finally, a fuel cell was fabricated using GDC/NLC nanocomposite electrolyte and its composite with NiO and LSCF as anode and cathode, respectively. The cell produced an excellent power density of 1.06 W/cm2 at 550 °C under fuel cell conditions. [Figure not available: see fulltext.]

Bench top stable transition metal (M = Co, Ni, Cu) complexes with a non-innocent ortho-aminophenol derivative were synthesized by the reaction of metal(II)acetates with a ligand precursor in 2:1 ratio. The solid-state structures reveal the formation of neutral molecular complexes with square planar coordination geometries. The Co(II) and Cu(II) complexes are paramagnetic, whereas the Ni complex is a diamagnetic square planar low-spin Ni(II) complex. All complexes, and Ni(II) complex in particular, show strong absorption in the near-IR region.

Colour can improve the visual aesthetics of solar cells for building and product integration but constitutes an optical loss from the perspective of photovoltaic energy conversion. To quantify this compromise, we report the theoretical efficiency limits of ideal coloured opaque single-band-gap solar cells. The colours were optimized by allowing the solar cells to reflect light within two distinct wavelength bands in the visible region. Colour chromaticity and brightness were controlled by modifying the position and width of the reflection bands, while optimising the band-gap energy for each colour. We found that almost the entire sRGB colour space has an efficiency limit greater than 29%, when relative luminosity is less than 0.25. This corresponds to a relative performance loss of less than 14% compared to an ideal black solar cell. Yellow-green is the most efficient photovoltaic colour, whereas highly saturated blue, red and purple colours produce the lowest efficiencies, when compared at equal brightness. The colour-dependence is explained by the photopic sensitivity of the human eye, which peaks at yellow-green wavelengths and tails towards the blue and red ends of the visible spectrum. For most colours, except the darkest ones, the optimal band-gap energy for a theoretically ideal solar cell is between 1.115 eV and 1.135 eV, matching the value for crystalline silicon. The results clarify the link between the solar cell colour and efficiency and establish a reference point and guidelines for optimizing coloured photovoltaics.

With electrocatalysts it is important to be able to distinguish between the effects of mass transport and reaction kinetics on the performance of the catalyst. When the hydrogen evolution reaction (HER) is considered, an additional and often neglected detail of mass transport in liquid is the evolution and transport of gaseous H2, since HER leads to the continuous formation of H2 bubbles near the electrode. We present a numerical model that includes the transport of both gaseous and dissolved H2, as well as mass exchange between them, and combine it with a kinetic model of HER at platinum (Pt) nanoparticle electrodes.We study the effect of the diffusion layer thickness and H2 dissolution rate constant on the importance of gaseous transport, and the effect of equilibrium hydrogen coverage and Pt loading on the kinetic and mass transport overpotentials. Gaseous transport becomes significant when the gas volume fraction is sufficiently high to facilitate H2 transfer to bubbles within a distance shorter than the diffusion layer thickness. At current densities below about 40 mA/cm2 the model reduces to an analytical approximation that has characteristics similar to the diffusion of H2. At higher current densities the increase in the gas volume fraction makes the H2 surface concentration nonlinear with respect to the current density. Compared to the typical diffusion layer model, our model is an extension that allows more detailed studies of reaction kinetics and mass transport in the electrolyte and the effects of gas bubbles on them.

Photovoltaics is amongst the most important technologies for renewable energy sources, and plays a key role in the development of a society with a smaller environmental footprint. Key parameters for solar cells are their energy conversion efficiency, their operating lifetime, and the cost of the energy obtained from a photovoltaic system compared to other sources. The optimization of these aspects involves the exploitation of new materials and development of novel solar cell concepts and designs. Both theoretical modeling and characterization of such devices require a comprehensive view including all scales from the atomic to the macroscopic and industrial scale. The different length scales of the electronic and optical degrees of freedoms specifically lead to an intrinsic need for multiscale simulation, which is accentuated in many advanced photovoltaics concepts including nanostructured regions. Therefore, multiscale modeling has found particular interest in the photovoltaics community, as a tool to advance the field beyond its current limits. In this article, we review the field of multiscale techniques applied to photovoltaics, and we discuss opportunities and remaining challenges. © T. Abu Hamed et al., published by EDP Sciences, 2018., European Cooperation in Science and Technology: MP1406, The authors are grateful for the financial support by the COST Action MP1406 “MultiscaleSolar.”

In this paper, a review of applying dye-sensitized (DSCs) and perovskite solar cells (PSCs) on flexible substrates is presented. Metallic and polymeric materials are the most common flexible substrates used. Cell integration into a textile substrate is also considered here as a future alternative. Common challenges with these include penetration of humidity, cell stability, and lifetime. Flexible DSCs and PSCs are still a niche technology, but have an inherent potential for cheap roll-to-roll mass production of photovoltaics.

Over the years numerous mixes of chemical compounds have been tried in the electrolytes of dye-sensitized solar cells in efforts to improve their efficiency. How these chemicals interact with each other and the photoelectrode has received surprisingly little attention. Here we report results from a systematic study of two I–/I3– electrolytes and their additives using infrared and Raman spectroscopy together with quantum chemical calculations. In the LiI electrolyte competing interactions between lithium cation and the solvent MPN and the additives TBP, NMBI, and GuSCN were identified. These interactions could inhibit the interaction of lithium ions with the TiO2 surface. It was found that under Raman excitation of PMII solution in contact with the photoelectrode, efficient generation of I3– takes place. For LiI solution, in addition, a Dye–I2 complex is formed. The results could be explained by diffusion-limited buildup of I3– and depletion of I– concentrations in the focal area of the excitation beam and by reduction of I3– via conduction band electrons of TiO2 beyond the focal region. To explain the formation of Dye–I2 complexes in the LiI electrolyte solutions a multistep regeneration mechanism is proposed. It was found that GuSCN reduces the I3– concentration in the electrolyte solutions studied; in the LiI electrolyte in addition it binds to lithium ions and nearly depletes the Dye–I2 complexes. From infrared spectra it became clear that preventing water from entering the DSCs during the preparation stages in ambient air is a demanding task. The identified interactions paint an intriguing new photochemical landscape of the function of the dye-sensitized solar cells giving guidelines for further development of the devices.

Rationale For commercialization of dye-sensitized solar cells (DSSCs), improvement of their long-term stability and efficiency is important. A key component in solar cells is the dye, its high purity and high stability. Here, methods for dye extraction and purification, and for determination of dye purity and dye degradation in DSSCs, were developed. Methods A method was developed for extraction of the dye Z907 from intact solar cells using a water/ethanol mixture containing tetrabutylammonium hydroxide. The N719 dye synthesized in our laboratory was purified by gel filtration on Sephadex LH20. These dyes, along with the dyes N3 and RuL2(NC)2, were analyzed using nuclear magnetic resonance (NMR) spectroscopy and liquid chromatography coupled to an electrospray ionization quadrupole-time-of-flight mass analyzer (LC/MS) operating in negative ionization mode. Results Purification of the synthesized N719 removed several impurities, including its undesired isomer with the thiocyanate ligand attached to ruthenium through sulfur instead of nitrogen. The dyes N719 and Z907 were successfully extracted from solar cells and together with N3 and RuL2(NC)2 analyzed by LC/MS, although N719 isomerized almost immediately in basic aqueous solution. The [M–H]−1 ions were observed and the measured mass was within a ±6 ppm range from the exact mass. Conclusions LC/MS in combination with NMR spectroscopy was shown to provide useful information on dye structure, purity, and on the efficiency of the purification methods. These methods allow for further studies of solar cell dyes, which may provide the detailed information needed for the improvement and eventual commercialization of the solar cell technology. Copyright © 2015 John Wiley & Sons, Ltd.

Solar-powered water splitting with photoelectrochemical (PEC) devices is a promising method to simultaneously harvest and store solar energy at a large scale. Highly efficient small prototype PEC devices reported recently demonstrate a move from basic material research toward design and engineering of complete devices and systems. The increased interest in engineering calls for a better understanding about the operational details of PEC devices at different length scales. The relevant physical phenomena and the properties of typical materials are well-known for separate device components, but their interaction in a complete PEC cell has received less attention. Coupled physical models are useful for studying these interactions and understanding the device operation as a whole and for optimizing the devices. We review the central physical processes in solar-powered water splitting cells and the physical models used in their theoretical simulations. Our focus is in particular on how different physical processes have been coupled together to construct device models and how different electrode and device geometries have been taken into account in them. Reflecting on the literature we discuss future opportunities and challenges in the modeling of PEC cells.

A semitransparent, flexible single-walled carbon nanotube (SWCNT) film was efficiently used in place of evaporated silver as the counter electrode of a poly(3,4-ethylenedioxythiophene) polymer-based solid-state dye solar cell (SSDSC): the solar-to-electrical energy conversion efficiency of the SWCNT-SSDSC was 4.8 % when it was 5.2 % for the Ag-SSDSC. The efficiency difference stemmed from a 0.1-V difference in the open-circuit voltage, whose reason was speculated to be related to the different recombination processes in the two types of SSDSCs.

Plasmonic metal nanoparticles have shown great promise in enhancing the light absorption of organic dyes and thus improving the performance of dye-sensitized solar cells (DSSCs). However, as the plasmon resonance of spherical nanoparticles is limited to a single wavelength maximum (e.g., ~ 520 nm for Au nanoparticles), we have here utilized silica-coated gold nanorods (Au@SiO2 NRs) to improve the performance at higher wavelengths as well. By adjusting the aspect ratio of the Au@SiO2 NRs, we can shift their absorption maxima to better match the absorption spectrum of the utilized dye (here we targeted the 600–800 nm range). The main challenge in utilizing anisotropic nanoparticles in DSSCs is their deformation during the heating step required to sinter the mesoporous TiO2 photoanode and we show that the Au@SiO2 NRs start to deform already at temperatures as low as 200 °C. In order to circumvent this problem, we incorporated the Au@SiO2 NRs in a TiO2 nanoparticle suspension that does not need high sintering temperatures to produce a functional photoanode. With various characterization methods, we observed that adding the plasmonic particles also affected the structure of the produced films. Nonetheless, utilizing this low-temperature processing protocol, we were able to minimize the structural deformation of the gold nanorods and preserve their characteristic plasmon peaks. This allowed us to see a clear redshift of the maximum in the incident photon-to-current efficiency spectra of the plasmonic devices (Δλ ~ 14 nm), which further proves the great potential of utilizing Au@SiO2 NRs in DSSCs.

The main issue in using low cost metals in dye solar cells is the corrosion caused by the liquid electrolyte. Contrary to typical applications of metals, the adverse effects of corrosion in dye solar cells are related to irreversible depletion of charge carriers from the electrolyte rather than consumption of the metal itself. It is calculated that the penetration rate due to corrosion should not exceed 10−4 mpy (a couple of nanometers per year) to ensure device lifetime longer than 1 year. This is 10 000 times slower rate than what is considered to be a general benchmark value for very low corrosion rate in the field of corrosion science and has a major effect on how corrosion should be investigated in the case of dye solar cells. Different methods, their applicability, and limitations to investigate corrosion in dye solar cells are evaluated here. The issue with most techniques is that they can detect metals that are clearly corroding, but they have significant limitations in proving a metal stable. Our investigation shows that the most reliable information on corrosion is obtained from complete dye solar cells that are exposed to working conditions. A combination of color analysis of the electrolyte to such measurement is proposed as a means to extrapolate future performance of the cells and estimate potential lifetimes of the dye solar cells in regards to corrosion. Copyright © 2014 John Wiley & Sons, Ltd.

We design a fully stable numerical solution of the Maxwell´s equations with the Transfer Matrix Method (TMM) to understand the interaction between an electromagnetic field and a finite, one-dimensional, nonperiodic structure. Such an exact solution can be tailored from a conventional solution by choosing an adequate transformation between its reference systems, which induces a mapping between its associated TMMs. The paper demonstrates theoretically the numerical stability of the TMM for the exact solution within the framework of Maxwell´s equations, but the same formalism can efficiently be applied to resolve other classical or quantum linear wave-propagation interaction in one, two, and three dimensions. This is because the formalism is exclusively built up for an in depth analysis of the TMM´s symmetries

3rd Generation photovoltaic systems such as dye-sensitized solar cells offer almost limitless material base that can be tested in variety of combinations with unique cell designs. One of the key challenges that remains with the dye-sensitized solar cells is to reduce their fabrication cost without compromising the performance. Such a target can only be achieved by fabricating inexpensive and abundantly available materials with simple and rapid preparatory methods that could deliver robust characteristics within the cell. With this motivation, we report here successful implementation of a highly conductive flexible fiber based substrate in dye-sensitized solar cell which is fabricated by coating a low temperature single walled carbon nanotube ink over a laminated fiber sheet. The substrate exhibited extraordinary durability under severe mechanical stability test conditions, reasonable overall efficiency (6.0±0.3%) and charge transfer resistance (3.3±1.6 Ω cm 2 ).

Volatile electrolytes are a stability concern in dye solar cells (DSCs) due to their tendency for leakage. A composite electrolyte consisting of iodide-based ionic liquid and polyaniline-coated carbon black has been previously reported to provide good current transport while being leakage proof due to a quasi-solid structure and the absence of volatile constituents. In this paper we investigate the operating principle of this type of electrolyte and especially its exceptional feature of operating efficiently without added iodine. The absence of additive iodine is significant due to the fact that it is usually required to form the current carrying the I–/I3– redox couple. We modified an electrolyte mass transport model from the literature to estimate the upper limit for the charge transport capability of the composite electrolyte. Comparison of experimental results with the estimated upper limit for the diffusion limiting current density shows clearly that the high current densities observed experimentally...

Yes. Testing 7 different metals as a substrate for a counter electrode in dye sensitized solar cells (DSSC) showed that some metals can be a good option for use with cobalt electrolyte. It was found that Stainless steels 304 and 321 as well as Ni and Ti suit well to the counter electrodes in DSSCs with cobalt electrolyte. In these 4 cases both the efficiency and the lifetime were similar to the reference cells on conducting glass substrates. In contrast, the cells with Al, Cu and Zn substrates suffered from both a low efficiency and a poor stability. These three metals had clear marks of corrosion such as apparent corrosion products in the aged cells. Additionally, we also investigated how the different types of catalyst materials perform in the case of a metal counter electrode (stainless steel 304) with cobalt electrolyte in comparison to reference glass cells. Among the 5 different catalyst layers the best results for stainless steel electrode were achieved with low temperature platinization whereas polymer catalysts poly(3,4-ethylenedioxythiophene)-p-toluenesulfone and poly(3,4-ethylenedioxythiophene)-polystyrenesulfone that worked well on the glass worked very poorly on the metal.

Dye solar cells (DSCs) are quite a new technology in photovoltaics. The traditional DSCs are prepared on conductively coated glass substrates in high temperature using a batch process. Manufacturing the cells on low-cost metal and plastic substrates would enable significant cost reductions as well as roll-to-roll mass production. There is a selection of metals and possible conducting coatings for plastics with varying electrical, optical, and chemical properties and price. The substrate has a dominant impact on the methods and materials that can be applied to make the cell and consequently on the resulting performance of the device. Furthermore, the substrates influence significantly the stability of the device. The main issue with plastics is their permeability whereas with metals, chemical stability in the electrolyte is the main concern. The leakage of electrolyte and the impact of water intake through the plastics can be affected by the material choices in particular with the electrolyte and dye composition. In the case of the metallic electrodes, the chemical stability can be improved by choosing a corrosion-resistant metal, applying a blocking layer or changing to a less aggressive electrolyte. One major focus of the current research of the flexible DSCs is increasing the efficiency by improved low-temperature preparation methods and materials especially for the photoelectrode. Another significant challenge is the development of noncorrosive electrolyte and dye combinations that work well even in the presence of significant amounts of water. C � 2012 John Wiley & Sons, Ltd.

The counter electrodes (CEs) for flexible dye solar cells (DSCs) are normally prepared by sputtering platinum on indium tin oxide (ITO) plastic substrate. However both ITO and platinum are expensive materials that need to be replaced with cheaper alternatives in large scale production of low-cost DSCs. We fabricated a flexible and completely carbon-based CE for DSCs based on electropolymerized poly (3,4-ethylenedioxythiophene) (PEDOT) on single-walled carbon nanotube (SWCNT) film on a plain plastic substrate. The DSCs with such a CE had an efficiency of 4.0%, which is similar to the efficiency of the reference DSCs (3.9%) based on conventional sputtered platinum on ITO-plastic CE. The carbon-based electrode was prepared by a simple press-transfer method of SWCNTs from the collection filter used in the gas phase synthesis and by electrochemical deposition of PEDOT on it. Electrochemical impedance spectroscopy confirmed that the PEDOT–SWCNT film had the best catalytic performance among the studied CE materials, and the film was also slightly transparent. The results demonstrate a successful combination of the conductive and catalytic properties of SWCNTs and PEDOT, respectively.

A simple and non-destructive method is introduced using image processing to investigate changes in the performance of the dye solar cells (DSCs). The main principle is based on the fact that the most important DSC components (dye, electrolyte, catalyst) have a specific color which often changes as result of degradation. Here the imaging technique is demonstrated in the case of exposing DSCs on very harsh conditions (85 °C temperature and UV + Visible light). The aging of the cells was recorded with a color sensitive camera in a well regulated setup and the photographs were processed using image analysis techniques. A key factor in making the imaging method quantitative and suitable for aging studies is color calibration which is explained in detail. The image analysis of different cell configurations revealed that the bleaching reactions of the electrolyte were related to reactions between TiO 2 and the electrolyte. The dye layer on the TiO 2 was shown slow down the degradation. Furthermore the comparison of image analysis and current–voltage curves indicated that the performance degradation of the cells was only partly due to loss of tri-iodide. The loss of photocurrent and photovoltage was apparently largely due to the harmful effect of the by-products of the bleaching and/or the degradation of the dye. In addition, a small recovery effect due to the generation of tri-iodide under reverse bias condition was seen in both image analysis and electrical measurements.

The characteristics of different types of catalyst layers based on Pt, polymer and carbon for flexible dye sensitized solar cells (DSSC) are investigated. These counter electrodes prepared at low temperature on indium doped tin oxide polyethyleneterephtalate (ITO-PET) plastic are compared with high temperature treated platinum and carbon catalyst layers on fluorine doped tin oxide (FTO) coated glass substrates. Here the electrical characteristics of the counter electrode and their optical performance are evaluated in order to compare their suitability for direct and reverse illumination. The morphology of the catalyst layers to the substrate is also investigated. Among the studied materials, the chemically platinized and carbon gel based counter electrodes demonstrated the

This review covers the current state of the art related to up-scaling and commercialization of dye solar cells (DSC). The cost analysis of the different components and manufacturing of DSC gives an estimate on the overall production costs. Moreover, it provides an insight in which areas improvement is needed in order to reach significant cost reductions. As a result of the cost analysis, transferring the technology to flexible substrates and employment of simple roll-to-roll production methods were found the key issues. The focus of this work was set accordingly. In this work, appropriate materials along with their unique fabrication processes and different design methods are investigated highlighting their advantages and limitations. The basic goal is to identify the best materials and preparation techniques suitable for an ideal roll-to-roll process of flexible dye solar module fabrication as well as the areas where further development is still needed.

Three characteristically different carbon nanomaterials were compared and analyzed as platinum-free counter electrodes for dye solar cells: 1) single-walled carbon nanotube (SWCNT) random network films on glass, 2) aligned multi-walled carbon nanotube (MWCNT) forest films on Inconel steel and quartz, and 3) pressed carbon nanoparticle composite films on indium tin oxide-polyethylene terephtalate plastic. Results from electrochemical impedance spectroscopy and electron microscopy were discussed in terms of the catalytic activity, conductivity, thickness, transparency and flexibility of the electrode films. The SWCNT films showed reasonable catalytic performance at similar series resistance compared to platinized fluorine doped tin oxide-coated glass. The MWCNTs had similar catalytic activity, but the electrochemical performance of the films was limited by their high porosity. Carbon nanoparticle films had the lowest charge transfer resistance resulting from a combination of high catalytic activity and dense packing of the material.

The purpose of this study was to identify stable metal based counter electrodes (CE) for dye solar cells (DSC). Previous studies have shown that stainless steel (StS 304) suffers from corrosion when used as a counter electrode. Therefore metals which have inherently higher corrosion resistance, such as stainless steel types 321, 316 and 316L, Inconel 600 and titanium, were investigated here. When using thermal platinization for the preparation of the catalyst layer on CE, only the titanium foil based metal based DSC remained consistently stable in the 1000 h light soaking test. The counter electrodes were also prepared with sputtering ∼20 nm thick layer of Pt which provides a highly uniform layer on the CE which acts also as a protective coating on the metal. With sputtered Pt, DSC on all studied metals expect for Inconel remained at 80–95% of the initial efficiency after light soaking test for 1000 h.

By deliberately introducing the thermally degraded form of the dye solar cell sensitizer N719 in dye-sensitized solar cells (DSCs) using synthetically prepared N719-TBP ([Ru(L-H)(2)(NCS)(4-tert-butylpyridine)](-+)N-(Bu)(4)), we have investigated the devastating influence of this ligand substitution product (N719-TBP) on the performance parameters of the cells. Two types of dyed solar cells, based on either N719 or N719-TBP, have been characterized employing standard current-voltage (I-V) performance test, UV-vis optical spectroscopy, incident photon to current efficiency (IPCE), and electrochemical impedance spectroscopy (EIS) methods. The performance tests show a drastic efficiency reduction of similar to 50% in the N719-TBP containing cells as compared to N719-dyed cells. The lower performance of N719-TBP was caused by lower overall light harvesting efficiency due to ca. 30 nm blue shift in the absorption spectrum of the dye, ca. 50% shorter electron diffusion length due to lower electron recombination resistance, and ca. 14% lower charge separation efficiency, which most likely can be ascribed to decreased dye regeneration efficiency caused by the replacement of one NCS ligand with TBP in the substitution product. The observations made in this study of DSC cells dyed with the substitution product, representing a worst case scenario of cells with 100% degraded dye, are in agreement with the characteristics of N719-dyed solar cells degraded at 85 degrees C, where the effect of ligand substitution is somewhat less pronounced.

A two-dimensional transient model of dye solar cells (DSC) describing the electrochemical reactions in the cell has been prepared. The model includes the relevant components of DSCs: the photoelectrode, the electrolyte, and the counter electrode. The solved variables are potential and the concentrations of the different ion species, which can be used to determine, e.g., the current−voltage characteristics of the cell. The largest benefit of this model is its 2D features which enable the study of lateral inhomogeneity. Using the model, a new phenomenon was described: lateral current density distribution caused by a small difference in the size between photoelectrode and counter electrode, typical of laboratory test cells, causes tri-iodide to move from the edge region to the active area of the cell. This process takes a relatively long time (8 min) and can be important for performance characterization and design of DSCs.

Design of new materials for nanostructured dye solar cells (DSC) requires understanding the link between the material properties and cell efficiency. This paper gives an overview of the fundamental and practical aspects of the modeling and characterization of DSCs, and integrates the knowledge into a user-friendly DSC device model. Starting from basic physical and electrochemical concepts, mathematical expressions for the IV curve and differential resistance of all resistive cell components are derived and their relation to electrochemical impedance spectroscopy (EIS) is explained. The current understanding of the associated physics is discussed in detail and clarified. It is shown how the model parameters can be determined from complete DSCs by current dependent EIS and incident-photon-to-collected-electron (IPCE) measurements, supplemented by optical characterization, and used to quantify performance losses in DSCs. The paper aims to give a necessary theoretical background and practical guidelines for establishing an effective feedback-loop for DSC testing and development.

Stainless steel based dye solar cells have been upscaled from small, laboratory size test cells of 0.32 cm2 active area to 6 cm x 6 cm "mini-modules" with active areas ca. 15 cm2. Stainless steel works as the photoelectrode substrate whilst the counter electrode is prepared on indium-doped tin oxide coated polyethyleneterephtalate or polyethylenenaphtalate plastic foil (fluorine-doped tin oxide coated glass as a reference). Additional current collector structures were deposited on the counter electrode substrate with inkjet-printing of silver nanoparticle ink in order to reduce the lateral resistance of the plastic foil. Flexible substrates enable roll-to-roll type industrial manufacturing of the cells and the steel's superior conductivity compared to the typical substrate materials such as glass and plastic makes it possible to prepare even substantially larger modules. The best efficiencies obtained this far with the "mini-module" using a stainless steel photoelectrode are 2.5% with a platinum-sputtered indium-doped tin oxide coated polyethyleneterephtalate counter electrode and 3.4% with a thermally platinized fluorine-doped tin oxide coated glass counter electrode. These efficiencies are on the same level than those measured with small cells prepared with similar methods and materials (3.4%-4.7%, depending on configuration, which are amongst the highest reported for this kind of a dye solar cell). Replacing expensive conducting glass with steel and plastic foils as the substrate materials leads also to economical savings in the cell production.

SUMMARY This review presents an overview of the current state of research on nanostructured titanium dioxide dye solar cells (DSCs) on alternative substrates to glass. Replacing the traditionally used heavy, rigid, and expensive glass substrate with materials such as plastic foils or metal sheets is crucial to enable large volume cost-efficient roll-to-roll type industrial scale manufacturing of the cells and to make this solar cell technology properly competitive with silicon and thin film photovoltaic devices. One of the biggest problems with plastic substrates is their low-temperature tolerance, which makes sintering of the photoelectrode films impossible, whereas with metals, their corrosion resistance against the iodine-containing electrolyte typically used in DSCs limits the amount of metal materials suitable for substrates. However, significant progress has been made in developing new materials, electrode film deposition and post-treatment methods suitable for low-temperature processing. Also, metals that do not corrode in the presence of iodine electrolyte have been found and successfully employed as DSC substrates. The highest power conversion efficiencies obtained with plastic and metal substrates are already 7–9%, which is not far from the best glass cell efficiencies, 10–11%, and comparable also to, for example, amorphous silicon solar cell efficiencies. One of the most important of the remaining research challenges of DSCs on flexible substrates is to ensure that the long-term stability of the cells is realistic to consumer applications, for example, with providing efficient enough encapsulation to prevent water and other impurities penetration into the cells. Degradation mechanisms specific to metal-based cells are another issue that needs deeper understanding still. More exotic approaches such as depositing the DSC structure on optical fiber or employing carbon nanomaterials to increase the cell efficiency are also discussed in this paper. Copyright r 2009 John Wiley & Sons, Ltd.

A new segmented cell design was applied to study the aging of dye solar cell with stainless steel (StS) photoelectrode substrate, in particular the role of electrolyte in the degradation. Photovoltaic characterization indicated that StS photoelectrode cells are subjected to rapid (within hours or days) performance degradation that did not occur in the StS counter electrode cells. Other complementary techniques, open circuit voltage decay (OCVD) and electrochemical impedance spectroscopy (EIS), showed changes in the recombination at the photoelectrode/electrolyte interface. With the segmented cell method, we confirmed that the electrolyte was not contaminated by the StS nor was it subject to other significant changes related to the rapid degradation.

This paper investigates how nonuniform generation and inefficient collection of electrons influence the dynamic photocurrent and photovoltage response of nanostructured photoelectrodes. The standard diffusion model theory of small amplitude light intensity modulated photocurrent (IMPS) and photovoltage (IMVS) spectroscopy is refined and generalized to an arbitrary electron generation profile, allowing straightforward coupling to any optical model. Expressions are derived for the local electron concentration and IMPS and IMVS transfer functions, for localized, uniform, and exponential generation profiles. Both limited collection and nonuniform generation of electrons modify the photoelectrode thickness (d) dependence of the characteristic IMPS and IMVS time constants and complicate their interpretation. This can lead to significant overestimation of the electron diffusion coefficient, diffusion length, and collection efficiency when using common approximate relations. With near contact electron generation, theIMPS response exhibits two time constants, only the slower one of which corresponds to electron transport across the film and scales with d. In the presence of this effect it is possible that in case of two equally thick samples, the one with smaller electron diffusion coefficient displays apparently faster electron transport. These errors demonstrated by experimental IMPS data of pressed TiO(2) photoelectrodes can be minimized by using modulated light incident from the counter electrode side and avoided when analyzing the ratio of IMPS at opposite directions Of illumination.

The factors that limit photocurrent in dye solar cells (DSC) were studied by incident-photon-to-collected-electron efficiency (eta(IPCE)), optical, and photovoltaic measurements. Nanostructured TiO2 photoelectrodes were prepared by compression technique on glass substrates, and half of them were given an additional heat treatment at 450 degrees C. The spectral absorbed-photon-to-collected-electron efficiency (eta(APCE)) of the cells was determined as a function of the photoelectrode film thickness (d) and direction of illumination and analyzed in terms of electron injection (eta(INJ)) and collection (eta(COL)) efficiency. The cells with pressed-only photoelectrodes gave significantly lower photocurrents yet their eta(APCE), and thus eta(COL), increased significantly with increasing d. To analyze this result quantitatively, methods were formulated based on the standard diffusion model of electron transport in nanostructured photoelectrodes for the factorization of experimental eta(APCF) data into eta(INJ) and eta(COL) parts and subsequent estimation of the effective steady-state electron diffusion length (L). Consistent decoupling of eta(INJ) and eta(COL) was reached in a spectral region where electron generation rate was independent of d. eta(INJ) was low and strongly wavelength-dependent, which was attributed to a poor energetic matching between dye excited states and TiO2 acceptor states due to unfavorable electrolyte composition. L increased systematically with d in both types of cells. Consistent with the increase of eta(IPCE) with light intensity, the result was attributed qualitatively to the electron concentration dependence of L and for a small part to decrease of film porosity with d. The diffusion model and its predictions were reviewed, and its validity in the present case was discussed critically.

The suitability of stainless steel for dye solar cell substrate was investigated with respect to performance and stability using photovoltaic characterization, electrochemical impedance spectroscopy (EIS), open circuit voltage decay (OCVD), and substrate polarization measurements. Stainless steel was employed both as photoelectrode and as counter electrode substrate gaining initial cell efficiencies of 4.7% and 3.5%, respectively. The leakage current from the stainless steel substrate was found to be very low. The effect of the stainless steel substrate on the performance of the other cell components was also examined. The traditional data analysis based on external cell voltage was shown to be inadequate and even misleading. Here, the voltage over a single cell component was determined computationally on the basis of EIS measurements as a function of cell current; through this approach, we found that the stainless steel counter electrode did not have any impact on the photoelectrode whereas the stainless...

The effect of repeated temperature variations on the performance of both fresh and aged dye-sensitized solar cells with liquid and semisolid electrolytes has been studied. The cell performance was characterized with IV-curves obtained at different cell operating temperatures and electrochemical impedance spectroscopy measurements before and after the temperature treatments. Consecutive temperature rampings of the aged cells did regenerate the cell function, so that the total efficiency drop over the observation period was on average 18%/unit less for the temperature-treated cells than for reference cells aged at constant temperature. r 2007 Elsevier B.V. All rights reserved.

For commercialization of dye-sensitized solar cells (DSSCs), improvement of their long-term stability and efficiency is important. A key component in solar cells is the dye, its high purity and high stability. Here, methods for dye extraction and purification, and for determination of dye purity and dye degradation in DSSCs, were developed.A method was developed for extraction of the dye Z907 from intact solar cells using a water/ethanol mixture containing tetrabutylammonium hydroxide. The N719 dye synthesized in our laboratory was purified by gel filtration on Sephadex LH20. These dyes, along with the dyes N3 and RuL2 (NC)2, were analyzed using nuclear magnetic resonance (NMR) spectroscopy and liquid chromatography coupled to an electrospray ionization quadrupole-time-of-flight mass analyzer (LC/MS) operating in negative ionization mode.Purification of the synthesized N719 removed several impurities, including its undesired isomer with the thiocyanate ligand attached to ruthenium through sulfur instead of nitrogen. The dyes N719 and Z907 were successfully extracted from solar cells and together with N3 and RuL2 (NC)2 analyzed by LC/MS, although N719 isomerized almost immediately in basic aqueous solution. The [M-H](-1) ions were observed and the measured mass was within a ±6 ppm range from the exact mass.LC/MS in combination with NMR spectroscopy was shown to provide useful information on dye structure, purity, and on the efficiency of the purification methods. These methods allow for further studies of solar cell dyes, which may provide the detailed information needed for the improvement and eventual commercialization of the solar cell technology.

Spray deposition of powder suspensions followed by room temperature compression was studied as a method for preparing nanostructured TiO 2 films for dye-sensitized solar cells. The structure of the films was analyzed with optical and scanning electron microscopy and the films were applied to dye-sensitized solar cells. Continuous and fast deposition of crack-free 7–14 μm thick films was achieved by heating the substrates during the deposition. Scanning electron microscopy revealed small amount of structural imperfections in the compressed films due to the nature of the deposition method. An energy conversion efficiency of 2.8% was achieved at 100 mW/cm 2 light intensity.

Electrochemical impedance spectroscopy was used to determine the effective charge transfer resistances of porous dye-sensitized solar cell counter electrodes prepared by low-temperature spray deposition and compression of conductive carbon and platinized Sb-doped SnO 2 powders on indium tin oxide-coated plastic substrates. The charge transfer resistances were 0.5–2 and 8–13 Ω cm 2 , respectively, when using 3-methoxypropionitrile as the electrolyte solvent. The manufacturing method used lends itself to produce mechanically stable and even-quality electrodes in an easy and fast manner.

A sensor developed for measurement of water concentration inside glass/polymer encapsulation structures with a particular application area in accelerated aging of photovoltaic module encapsulants is described. An approximately 5 μm thick porous TiO 2 film applied to a glass substrate with a conductive coating acts as the moisture-sensitive component. The response is calibrated with weather chamber experiments for sensors open to the environment and with diffusion experiments for sensors laminated under an encapsulant. For the interpretation of diffusion experiment results, a transport model describing the diffusion of water across the polymer/TiO 2 interface is developed. The logarithm of AC resistance shows a linear dependence on water concentration in both open and encapsulated calibration. The first measurable response from an encapsulated 3.5 mm × 8 mm size sensor is obtained when approximately 10 μg of water has entered the film. Implications of the calibration results for sensor usage in accelerated aging tests are discussed.

The recent surge in investigating electrocatalysts for the H2 evolution reaction is based on finding a cheap alternative to Pt. However platinum’s excellent catalytic activity means very little catalyst needs to be used. The present study combines model experiments with numerical modeling to determine exactly how little catalyst is needed. Specifically we investigate ultra-low Pt loadings for use in photoelectrochemical H2 evolution using TiO2–Ti-pn+Si photocathodes. At a current density of 10 mA cm-2, we photocathodically evolve H2 at +465, +450, +350 and +270 mV vs., RHE at Pt loadings of 1000, 200, 50, and 10 ng cm-2 corresponding to HER overpotentials of η1000ng = 32 mV, η200ng = 46mV, η50ng = 142 mV, and η10ng = 231 mV. To put this in perspective, if 30% of the world’s current annual Pt production was used for H2 evolution catalysis, using a loading of 100 ng cm-2 and a current of 10 mA cm-2 would produce 1 TWaverage of H2. The photoelectrochemical data matched the modeling calculations implying that we were near the fundamental maximum in performance for our system. Furthermore modeling indicated that the overpotentials were dominated by mass transfer effects, rather than catalysis unless catalyst loadings were less than 1000 ng cm-2.