a b s t r a c tPerovskite solar cells have attracted attention due its high conversion efficiency and low cost. In this work, Nb 2 O 5 is used as an alternative compact hole blocking layer in conjunction with mesoporous TiO 2 and CH 3 NH 3 PbI 3 in perovskite solar cells. The influence of Nb 2 O 5 layer thickness was studied and it was found to strongly influence the J-V hysteresis of the cells. Devices constructed with 50 nm Nb 2 O 5 have small or undetectable hysteresis, which becomes detectable and increases with increasing Nb 2 O 5 layer thickness. For the best device, energy conversion efficiency of up to 12%, short-circuit currents of 17 mA/cm 2 and fill factors of 74% were found. These parameters are comparable to the best performance of similar devices where the compact layer is TiO 2 . In addition, the use of Nb 2 O 5 improved the stability of the solar cells under illumination. These improvements are attributed to a better extraction of photogenerated electrons in the perovskite layer.
A simple lamination process of the top electrode for perovskite solar cells is demonstrated. The laminate electrode consists of a transparent and conductive plastic/metal mesh substrate, coated with an adhesive mixture of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate), PEDOT:PSS, and sorbitol. The laminate electrode showed a high degree of transparency of 85%. Best cell performance was achieved for laminate electrodes prepared with a sorbitol concentration of ~30 wt% per milliliter PEDOT:PSS dispersion, and using a pre-annealing temperature of 120°C for 10 min before lamination. Thereby, perovskite solar cells with stabilized power conversion efficiencies of (7.6 ± 1.0)% were obtained which corresponds to 80% of the reference devices with reflective opaque gold electrodes.
TiO 2 derivatives with distinct morphologies have been successfully obtained by microwave assisted hydrothermal synthesis in acidic and alkaline medium using mild conditions. Titanium tetraisopropoxide (TTIP) was used as precursor in different environmental conditions under low temperatures, inferior to 150 °C, and short synthesis times, from 2 to 60 min. X ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and N 2 adsorption at 77 K (BET) were used to characterize the microstructural properties of the oxides. In the acidic synthesis the reaction time and temperature are not accompanied by significant changes in the structure of the material. However, in the basic conditions, the concentration of Na + ions strongly influences the particle morphology and growth. The morphology of the nanoparticles shows irregular spheres in acidic conditions, while in alkaline medium, needle like structures are formed as well as aggregated nanotube-like structures synthesized in only 30 min. Besides the difference in the morphology and structure, in both systems, high surface area was obtained.
Biocompatible and biodegradable powering materials are appealing systems for biomedical and electronic devices. Melanin is a natural and multifunctional material with redox capability, which is of great interest in electrochemical energy storage functionalities. In our work, we explored the use of soluble melanin derivatives as active materials for symmetric solid-state supercapacitors operating in the dark and under illumination. We observed that our devices were photo-pseudocapacitive. Additionally, under illumination, our best device showed a specific capacitance of 57.7 mFg−1 at a scan rate of 0.01 Vs−1, with a decrease of 53% in resistance compared to that in the dark. Our outcome suggests that soluble melanin is a promising material for solid-state powering elements in wearable and environmentally friendly devices.
In this work, niobium oxide films were deposited by reactive magnetron sputtering under different oxygen flow rate and applied as electron transport layer in perovskite solar cells. It was found that the deposition made using 3.5 sccm of oxygen flow resulted in films with better electrical properties which helped the extraction of the photogenerated electrons to the external circuit, improving the Jsc and consequently the device efficiency. In addition, by photoluminescence measurements, we found a better charge transfer from perovskite to TiO2/niobium oxide film deposited at 3.5 sccm of oxygen flow.
<p>Two different methods are used to deposit Nb2O5 as compact electron transport layers in n-i-p double cation mixed-halide perovskite Cs0.17FA0.83Pb(I0.83Br0.17)3 solar cells; reactive sputtering and spin coating. These different Nb2O5 films influenced perovskite growth and the charge transport in the cells. Photovoltaic parameters were obtained with an average PCE of 17.0 % and 15.7% for the devices based on sputtered and spin-coated Nb2O5, respectively. The mobility and the extracted charges were higher in sputtered Nb2O5-based devices than in the spin-coated ones. This effect is attributed to the larger grain sizes observed in the perovskite films when deposited onto the sputtered Nb2O5 layers. The higher densities of grain boundaries in the spin-coated Nb2O5-based devices increase ion diffusion and are expected to decrease efficiency.
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