Super-Droplet-Repellent Carbon-Based Printable Perovskite Solar Cells.

Despite attractive cost-effectiveness, scalability, and superior stability, carbon-based printable perovskite solar cells (CPSCs) still face moisture-induced degradation that limits their lifespan and commercial potential. Here, the moisture-preventing mechanisms of thin nanostructured super-repellent coating (advancing contact angle >167° and contact angle hysteresis 7°) integrated into CPSCs are investigated for different moisture forms (falling water droplets vs water vapor vs condensed water droplets). It is shown that unencapsulated super-repellent CPSCs have superior performance under continuous droplet impact for 12 h (rain falling experiments) compared to unencapsulated pristine (uncoated) CPSCs that degrade within seconds. Contrary to falling water droplets, where super-repellent coating serves as a shield, water vapor is found to physisorb through porous super-repellent coating (room temperature and relative humidity, RH 65% and 85%) that increase the CPSCs performance for 21% during ≈43 d similarly to pristine CPSCs. It is further shown that water condensation forms within or below the super-repellent coating (40 °C and RH 85%), followed by chemisorption and degradation of CPSCs. Because different forms of water have distinct effects on CPSC, it is suggested that future standard tests for repellent CPSCs should include rain falling and condensate formation tests. The findings will thus inspire the development of super-repellent coatings for moisture prevention.

Advanced research trends in dye-sensitized solar cells.

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.

Colors of Single-Wall Carbon Nanotubes.

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.

An analytical model of hydrogen evolution and oxidation reactions on electrodes partially covered with a catalyst.

Our previous theoretical study on the performance limits of the platinum (Pt) nanoparticle catalyst for the hydrogen evolution reaction (HER) had shown that the mass transport losses at a partially catalyst-covered planar electrode are independent of the catalyst loading. This suggests that the two-dimensional (2D) numerical model used could be simplified to a one-dimensional (1D) model to provide an easier but equally accurate description of the operation of these HER electrodes. In this article, we derive an analytical 1D model and show that it indeed gives results that are practically identical to the 2D numerical simulations. We discuss the general principles of the model and how it can be used to extend the applicability of existing electrochemical models of planar electrodes to low catalyst loadings suitable for operating photoelectrochemical devices under unconcentrated sunlight. Since the mass transport losses of the HER are often very sensitive to the H2 concentration, we also discuss the limiting current density of the hydrogen oxidation reaction (HOR) and how it is not necessarily independent of the reaction kinetics. The results give insight into the interplay of kinetic and mass-transport limitations at HER/HOR electrodes with implications for the design of kinetic experiments and the optimization of catalyst loadings in the photoelectrochemical cells.

Analysis of dye degradation products and assessment of the dye purity in dye-sensitized solar cells.

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.

Effect of electrolyte bleaching on the stability and performance of dye solar cells.

Degradation of dye solar cells (DSCs) under severe ageing conditions may lead to loss of the tri-iodide in the electrolyte - a phenomenon known as electrolyte bleaching. Monitoring changes in the tri-iodide concentration as a result of degradation mechanisms and understanding their causes and effects are fundamental for improving the long-term stability of DSCs. In this contribution a strongly accelerated ageing test (1 Sun visible light, 1.5 Suns UV light, T = 110 °C for 12 h) was performed on DSCs in a double-sealed masterplate configuration to purposely induce severe electrolyte bleaching, and its effects on the performance and stability of DSCs with different initial tri-iodide concentrations [I3(-)]0 were investigated. The cells with low [I3(-)]0 suffered a severe loss in short circuit current density JSC (up to 85%). Also a significant loss of open circuit voltage VOC was observed and this loss was proportional to [I3(-)]0 with the highest VOC drop observed with the highest [I3(-)]0. Non-destructive analysis techniques based on the limited current density, JSCvs. light intensity, and photographic image analysis, were used to quantify the [I3(-)] loss, which was found to be ca. 50 mM and independent of [I3(-)]0. Quantitative model based VOC analysis in terms of changing [I3(-)] revealed that the degradation responsible for the VOC drop was dominated by an unknown mechanism that is unrelated to [I3(-)]0. The methods and results reported here help separating and identifying different degradation mechanisms related to electrolyte bleaching in DSCs.

High performance low temperature carbon composite catalysts for flexible dye sensitized solar cells.

Roll-to-roll manufacturing of dye sensitized solar cells (DSSCs) requires efficient and low cost materials that adhere well on the flexible substrates used. In this regard, different low temperature carbon composite counter electrode (CE) catalyst ink formulations for flexible DSSCs were developed that can be simply and quickly coated on plastic substrates and dried below 150 °C. The CEs were investigated in terms of photovoltaic performance in DSSCs by current-voltage measurements, mechanical adhesion properties by bending and tape tests, electro-catalytic performance by electrochemical impedance spectroscopy and microstructure by electron microscopy. In the bending and tape tests, PEDOT-carbon composite catalyst layers exhibited higher elasticity and better adhesion on all the studied substrates (ITO-PET and ITO-PEN plastic, and FTO-glass), compared to a binder free carbon composite and a TiO2 binder enriched carbon composite, and showed lower charge transfer resistance (1.5-3 Ω cm(2)) than the traditional thermally platinized CE (5 Ω cm(2)), demonstrating better catalytic performance for the tri-iodide reduction reaction. Also the TiO2 binder enriched carbon composite showed good catalytic characteristics and relatively good adhesion on ITO-PET, but on ITO-PEN its adhesion was poor. A DSSC with the TiO2 binder enriched catalyst layer reached 85% of the solar energy conversion efficiency of the reference DSSC based on the traditional thermally platinized CE. Based on the aforementioned characteristics, these carbon composites are promising candidates for replacing the platinum catalyst in a high volume roll-to-roll manufacturing process of DSSCs.

Linking optical and electrical small amplitude perturbation techniques for dynamic performance characterization of dye solar cells.

This paper unifies the analytical models used widely but thus far mostly separately for electrical and optical small amplitude perturbation measurements of nanostructured electrochemical dye solar cells (DSC): electrochemical impedance spectroscopy (EIS), intensity-modulated photocurrent spectroscopy (IMPS) and intensity-modulated photovoltage spectroscopy (IMVS). The models are linked by expressing the kinetic boundary condition used for solving the time-dependent continuity equation of electrons in IMPS and IMVS analysis in terms of the series and parallel impedance components found in the complete equivalent circuit impedance model of DSC. As a result, analytical expressions are derived for potentiostatic IMPS and galvanostatic IMVS transfer functions of complete DSCs that are applicable at any operating point along the solar cell current-voltage (IV) curve. In agreement with the theory, impedance spectrum calculated as a ratio of IMVS and IMPS transfer functions measured near the maximum power point matches exactly with the impedance spectrum measured directly with EIS. Consequently, both IMPS-IMVS and EIS yield equal estimates for the electron diffusion length. The role of the chemical capacitance of the nanostructured semiconductor photoelectrode in the interpretation of the so-called RC attenuation of the IMPS response is clarified, as well as the capacitive frequency dispersion in IMPS and IMVS.

Device physics of dye solar cells.

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.

Thin film nano solar cells--from device optimization to upscaling.

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.