Abstract In this work, CH3NH3PbI3 perovskite thin films were deposited by the spray-coating method in ambient conditions using different deposition temperatures and annealing times. They were then exposed to high humidity in order to investigate the relation between processing parameters and degradation mechanisms. FTIR and XRD analyses identified two degradation mechanisms, one reversible, the formation of monohydrated perovskite, CH3NH3PbI3∙H2O, and another irreversible, the decomposition of perovskite into PbI2 and CH3NH3I. It was found that perovskite degradation is very sensitive to deposition parameters and that long annealing times at high temperatures increase compound stability, retarding reversible degradation even after a long exposure to ambient conditions. This is attributed to the formation of a small amount of PbI2 during deposition that acts as a protective layer against moisture, preventing the formation of monohydrated perovskite. Additionally, no signs of dihydrated perovskite were found in the films even after 50 days of exposure to high humidity.

The optimization of fuel cell materials, particularly polymer membranes, for PEMFC has driven the development of methods and alternatives to achieve systems with more adequate properties to this application. The sulfonation of poly (styrene-co-allyl alcohol) (PSAA), using sulfonating agent:styrene ratios of 2:1, 1:1, 1:2, 1:4, 1:6, 1:8 and 1:10, was previously performed to obtain proton conductive polymer membranes. Most of those membranes exhibited solubility in water with increasing temperature and showed conductivity of approximately 10-5 S cm-1. In order to optimize the PSAA properties, especially decreasing its solubility, semi-IPN (SIPN) membranes are proposed in the present study. These membranes were obtained from the diglycidyl ether of bisphenol A (DGEBA), curing reactions in presence of DDS (4,4-diaminodiphenyl sulfone) and PSAA. Different DGEBA/PSAA weight ratios were employed, varying the PSAA concentration between 9 and 50% and keeping the mass ratio of DGEBA:DDS as 1:1. The samples were characterized by FTIR and by electrochemical impedance spectroscopy. Unperturbed bands of PSAA were observed in the FTIR spectra of membranes, suggesting that chemical integrity of the polymer is maintained during the synthesis. In particular, bands involving C-C stretching (1450 cm-1), C=C (aromatic, ~ 3030 cm-1) and C-H (2818 and 2928 cm-1) were observed, unchanged after the synthesis. The disappearance or reduction of the intensity of the band at 916 cm-1, attributed to the DGEBA epoxy ring, is evidenced for all samples, indicating the epoxy ring opening and the DGEBA crosslinking. Conductivity of H3PO4 doped membranes increases with temperature, reaching 10-4 S cm-1.