Research Update: Behind the high efficiency of hybrid perovskite solar cells

Perovskite solar cells (PSCs) marked tremendous progress in a short period of time and offer bright hopes for cheap solar electricity. Despite high power conversion efficiency >20%, its poor operational stability as well as involvement of toxic, volatile, and less-abundant materials hinders its practical deployment. The fact that degradation and toxicity are typically observed in the most successful perovskite involving organic cation and toxic lead, i.e., CH3NH3PbX3, requires a deep understanding of their role in photovoltaic performance in order to envisage if a non-toxic, stable yet highly efficient device is feasible. Towards this, we first provide an overview of the basic chemistry and physics of halide perovskites and its correlation with its extraordinary properties such as crystal structure, bandgap, ferroelectricity, and electronic transport. We then discuss device related aspects such as the various device designs in PSCs and role of interfaces in origin of PV parameters particularly open circuit voltage, various film processing methods and their effect on morphology and characteristics of perovskite films, and the origin and elimination of hysteresis and operational stability in these devices. We then identify future perspectives for stable and efficient PSCs for practical deployment

Effect of TiO2 Photoanode Porosity on Dye Diffusion Kinetics and Performance of Standard Dye-Sensitized Solar Cells

Low-cost water-based P25-TiO2 pastes were formulated and used to produce porous TiO2 films in application to the fabrication of dye-sensitized solar cells. The structural properties of the films were characterized using a variety of techniques such as stylus profilometry, FEG-SEM imaging, BET surface area, and BJH pore size analyses. These were compared to films produced from a commercial paste, DSL 18 NR-AO (Dyesol). The major difference was in the fraction of macroporosity: 23% of the total pore volume for films produced with the commercial material and 67–73% for the P25-TiO2 films owing to the vast difference in dispersion and size distribution of the particles in the two types of pastes. The macroporosity was found to have a dramatic effect on the dye diffusion kinetics measured using in situ UV-Vis reflectance spectroscopy. The sensitization of P25-based films was much faster for heavily macroporous P25-TiO2 films (>90% saturation at 15–35 mins) than for their commercial analogue (>90% saturation at 110 mins). DSC devices built with optimized P25-TiO2 photoanodes showed better performance at short dye immersion time (30 mins and 1 hr) due to faster percolation of the dye molecules through the film

Radiation Hardness of Perovskite Solar Cells Based on Aluminum‐Doped Zinc Oxide Electrode Under Proton Irradiation

Due to their high specific power and potential to save both weight and stow volume, perovskite solar cells have gained increasing interest to be used for space applications. However, before they can be deployed into space, their resistance to ionizing radiations such as high‐energy protons must be demonstrated. In this report, we investigate the effect of 150 keV protons on the performance of perovskite solar cells based on aluminium‐doped zinc oxide (AZO) transparent conducting oxide (TCO). Record power conversion efficiency of 15% and 13.6% were obtained for cells based on AZO under AM1.5G and AM0 illumination, respectively. We demonstrate that perovskite solar cells can withstand proton irradiation up to 1013 protons.cm−2 without significant loss in efficiency. At this irradiation dose, Si or GaAs solar cells would be completely or severely degraded when exposed to 150 keV protons. From 1014 protons.cm−2, a decrease in short‐circuit current of the perovskite cells is observed, which is consistent with interfacial degradation due to deterioration of the Spiro‐OMeTAD HTL during proton irradiation. Using a combination of non‐destructive characterization techniques, results suggest that the structural and optical properties of perovskite remain intact up to high fluence levels. Although shallow trap states are induced by proton irradiation in perovskite bulk at low fluence levels, they can release charges efficiently and are not detrimental to the cell's performance. This work highlights the potential of perovskite solar cells based on AZO TCO to be used for space applications and give a deeper understanding of interfacial degradation due to proton irradiation

Photoelectrocatalytic Surfactant Pollutant Degradation and Simultaneous Green Hydrogen Generation

For the first time, we demonstrate a photoelectrocatalysis technique for simultaneous surfactant pollutant degradation and green hydrogen generation using mesoporous WO$_3$/BiVO$_4$ photoanode under simulated sunlight irradiation. The materials properties such as morphology, crystallite structure, chemical environment, optical absorbance, and bandgap energy of the WO$_3$/BiVO$_4$ films are examined and discussed. We have tested the anionic type (sodium 2-naphthalenesulfonate (S2NS)) and cationic type surfactants (benzyl alkyl dimethylammonium compounds (BAC-C12)) as model pollutants. A complete removal of S2NS and BAC-C12 surfactants at 60 and 90 min, respectively, by applying 1.75 V applied potential vs RHE to the circuit, under 1 sun was achieved. An interesting competitive phenomenon for photohole utilization was observed between surfactants and adsorbed water. This led to the formation of H$_2$O$_2$ from water alongside surfactant degradation (anode) and hydrogen evolution (cathode). No byproducts were observed after the direct photohole mediated degradation of surfactants, implying its advantage over other AOPs and biological processes. In the cathode compartment, 82.51 μmol/cm$^2$ and 71.81 μmol/cm$^2$ of hydrogen gas were generated during the BAC-C12 and S2NS surfactant degradation process, respectively, at 1.75 V RHE applied potential

Acetonitrile based single step slot-die compatible perovskite ink for flexible photovoltaics

The demonstration of photovoltaic devices with high power conversion efficiencies using low cost perovskite materials hints at the possibility of dramatically lowering the cost of solar energy. Key to further exploiting the potential of these materials is developing rapid processing techniques that can be used to deliver lower cost high throughput manufacture. This work details the development of low viscosity rapid drying perovskite formulations designed to give high quality solar films when slot-die coated on flexible roll-to-roll compatible substrates. A single step slot-die compatible perovskite ink based on an acetonitrile/methylamine solvent system utilizing a chloride additive is developed, resulting in large area perovskite films from slot-die coating under ambient conditions. The drying conditions for the perovskite film are optimized and fast (<10 min), low temperature (<120 °C) drying of slot-die coated films on flexible substrates are demonstrated and result in high performance devices

Studies of inherent lubricity coatings for low surface roughness galvanised steel for automotive applications

Surface lubricity on TiO2-coated galvanised steels can be controlled by solution depositing perfluorooctanoic (C8), lauric (C12) or stearic (C18) acids to avoid lubricating oils/emulsions or substrate pre-etching to remove surface oxide that add cost and waste. Water contact angles reveal increased surface hydrophobicity on coated samples that correlate with linear friction testing, suggesting water contact angle can be used to screen lubricity compounds. Linear friction testing shows that C12 and C18 lower the coefficient of friction (μ) by 50–60% compared with uncoated substrates whilst C8 drops μ from 0.31 to 0.22. Surfaces have been characterised by X-ray photoelectron spectroscopy, scanning electron microscopy and atomic force microscopy, whilst infrared confirms that as-deposited coatings contain physisorbed and deprotonated acids chemisorbed through esters and thermal gravimetric analysis confirms increasing loadings from C8 to C12 to C18. Surface washing removes physisorbed material and lowers μ by increasing surface organisation and alkyl chain packing that enhances frictional energy dissipation through steric quenching

Proton Radiation Hardness of Perovskite Solar Cells Utilizing a Mesoporous Carbon Electrode

Funder: Airbus Endeavr WalesFunder: Alexander von Humboldt FoundationWhen designing spacefaring vehicles and orbital instrumentation, the onboard systems such as microelectronics and solar cells require shielding to protect them from degradation brought on by collisions with high‐energy particles. Perovskite solar cells (PSCs) have been shown to be much more radiation stable than Si and GaAs devices, while also providing the ability to be fabricated on flexible substrates. However, even PSCs have their limits, with higher fluences being a cause of degradation. Herein, a novel solution utilizing a screen‐printed, mesoporous carbon electrode to act bi‐functionally as an encapsulate and the electrode is presented. It is demonstrated that the carbon electrode PSCs can withstand proton irradiation up to 1 × 1015 protons cm−2 at 150 KeV with negligible losses (<0.07%) in power conversion efficiency. The 12 μm thick electrode acts as efficient shielding for the perovskite embedded in the mesoporous TiO2. Through Raman and photoluminescence spectroscopy, results suggest that the structural properties of the perovskite and carbon remain intact. Simulations of the device structure show that superior radiation protection comes in conjunction with good device performance. This work highlights the potential of using a carbon electrode for future space electronics which is not limited to only solar cells

Perovskite Photovoltaic Modules: Life Cycle Assessment of Pre-industrial Production Process

Photovoltaic devices based on perovskite materials have a great potential to become an exceptional source of energy while preserving the environment. However, to enter the global market, they require further development to achieve the necessary performance requirements. The environmental performance of a pre-industrial process of production of a large-area carbon stack perovskite module is analyzed in this work through life cycle assessment (LCA). From the pre-industrial process an ideal process is simulated to establish a benchmark for pre-industrial and laboratory-scale processes. Perovskite is shown to be the most harmful layer of the carbon stack module because of the energy consumed in the preparation and annealing of the precursor solution, and not because of its Pb content. This work stresses the necessity of decreasing energy consumption during module preparation as the most effective way to reduce environmental impacts of perovskite solar cells