The development of efficient, stable, and non-precious metal water oxidation catalysts (WOCs) is a matter of importance for sustainable energy research. In this work, iron cobaltite (FeCo2O4) nanoparticles were prepared by the coprecipitation method, and we present the effect of heat treatment (250, 350, 450, 650 and 900 °C) on the catalytic properties. Catalytic activity tests of FeCo2O4 nanocatalysts were performed in the presence of ammonium cerium(IV) nitrate (CAN), and the formation of oxygen was followed using a Clark-type oxygen electrode. The samples were characterized by infrared (IR), thermogravimetric analysis (TGA), powder X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS), and their surface areas were determined by the Brunauer, Emmett, and Teller (BET) method. Fourier transform infrared (FTIR) data confirm a metal-oxygen bond at the octahedral and tetrahedral sites. XRDs data were characteristic of spinel-like cubic materials. The XPS results confirmed the presence of trivalent and divalent cobalt and iron ions in the samples and showed that the non-heated sample has a greater amount of cobalt on the nanoparticles’ surface than those heated to 900 °C. The surface area decreased from 92.00 m2 g-1 for the material that was unannealed to 2.00 m2 g-1 for the sample annealed at 900 °C. The unannealed nanomaterials showed an oxygen production of 790 mmol s-1 g-1. This was 790 times greater than the oxygen production from nanomaterials heated to 900 °C. Although the surface structure of nanomaterials is unclear, the amount of surface cobalt appears to have implications for catalytic activity. Optimization of superficial cobalt content may be key to improving catalytic activity.

Flavonoids are polyphenolic compounds widespread in vegetal kingdom. They present a C-15 skeleton, which is divided into three units A, B and C. Unit C is an oxygen containing heterocyclic, whose oxidation state and saturation level define major subclasses. Units A and B are aromatic rings, in which four major types of substituents, i. e. hydroxyl, methoxyl, prenyl and glycosides, lead to over 8000 different flavonoids. The great healthy-protecting value of these phytochemical biomarkers has attracted the attention of scientific community. Their main biological actions include anticancer and anti-inflammatory properties, which are strictly linked to antioxidant activities. So that, electroanalysis have been extensively applied on mechanistic studies and also for analytical determinations. This review presents the state of the art regarding the main applications of electroanalysis on the flavonoid research. The approaches on redox behavior characterization leading to a better understanding of structure antioxidant activity relationships are highlighted.

A new electroanalytical method coupling TLC-DPV in solid state was developed for quantitative determination of phytoantioxidants with medicinal purpose, e.g. rosmarinic acid (RA) in samples of phytopharmaceuticals, e.g. rosemary (Rosmarinus officinalis L.). The method showed to be feasible, presenting linearity in concentrations ranging from 0.694 x 10-3 to 9.526 x 10-3 mol L-1 (r = 0.9945), good sensibility, selectivity, reproducibility, repeatability, agility and affordable cost. The concentrations of RA in different extracts of rosemary ranged from 0.05 to 0.52 (% w/w), presenting high recovery levels when compared to HPLC.