RESUMO
Mixed halide perovskites have attracted a strong interest in the photovoltaic community as a result of their high power conversion efficiency and the solid opportunity to realize low-cost and industry-scalable technology. Light soaking represents one of the most promising approaches to reduce non-radiative recombination processes and thus to optimize device performances. Here, we investigate the effects of 1 sun illumination on state-of-the-art triple cation halide perovskite thin films Cs0.05(MA0.14, FA0.86)0.95 Pb (I0.84, Br0.16)3 by a combined optical and chemical characterization. Competitive passivation and degradation effects on perovskite transport properties have been analyzed by spectrally and time-resolved quantitative imaging luminescence analysis and by X-ray photoemission spectroscopy (XPS). We notice a clear improvement of the optoelectronic properties of the material, with a increase of the quasi fermi level splitting and a corresponding decrease of methylammonium MA+ for short (up to 1 h) light soaking time. However, after 5 h of light soaking, phase segregation and in-depth oxygen penetration lead to a decrease of the charge mobility.
RESUMO
Reflux of a solution of [Ti8 O12 (H2 O)24 ]Cl8 â HClâ 7 H2 O as titanium precursor at 120 °C for 24â h leads to a transparent colloidal solution of nanosized crystallized anatase TiO2 . The adjustment of the particle size and composition of the dispersant is monitored through the initial water content while controlling the conversion of propylene carbonate into propylene glycol during reflux. The solutions were processed as thin films to produce electron transporting layers in hybrid bulk heterojunction solar cells, by using a blend of P3HT:PCBM polymers as absorbers, in inverted architectures. The solutions obtained by reflux were demonstrated to produce suitable electron transporting layers.
