Dye-sensitized solar cells using natural dyes have lower cost when compared to ruthenium-based dyes. This paper aims to evaluate, electrochemically, solar cells composed of TiO2 with dye extracted from the Hibiscus(var. Sabdariffa) and propose an adsorption model capable of predicting the adsorption mechanism of the dye on the semiconductor surface. The characterization techniques used were: Fourier Transform Infrared Spectroscopy, UV-VIS Spectroscopy, Measurement of the Open Circuit Potential, Photocronoamperometry, and Current Density Curves vs. Potential. The infrared spectroscopy confirmed there was adsorption of dye on the TiO2 surface. The adsorption isotherm with the better value of linear coefficient (R= 0.9874) was the Langmuir isotherm. The electrochemical techniques showed that the best cell prepared from a solution with a concentration of 5.27 mg L-1 of the natural dye, had an Eca= 516 mV, j = 0.15 mA cm-2 and an energy efficiency (η) of 0.15%.

In this work the preparation and characterization of a supported catalyst intended for degradation of reactive dyes by Fenton-like processes is described. The photocatalyst was prepared by immobilization of Fe3+ into the molecular sieve (4A type) surface and characterized by x-ray diffractometry and infrared, Mössbauer and EPR spectroscopy. The solid containing 0.94% (w/w) of ferric ions was used in degradation studies of aqueous reactive-dyes samples with really promissory results. Generally, Vis-assisted photochemical processes leads to almost total decolorization of all tested dyes at reaction times lower than 30 min. It was also observed that the iron-molecular sieve matrix can be reused.