RESUMO
Aiming to improve the photocatalytic properties of transition metal perovskites to be used as robust photoanodes, [LaFeO3]1-x/[SrTiO3]x nanocomposites (LFO1-x/STOx) are considered. This hybrid structure combines good semiconducting properties and an interesting intrinsic remanent polarization. All the studied samples were fabricated using a solid-state method followed by high-energy ball milling, and they were subsequently deposited by spray coating. The synthesized compounds were demonstrated to possess orthorhombic (Pnma) and cubic (Pm3¯m) structures for LFO and STO, respectively, with an average grain size of 55-70 nm. The LFO1-x/STOx nanocomposites appeared to exhibit high visible light absorption, corresponding to band gaps of 2.17-3.21 eV. Our findings show that LFO0.5/STO0.5 is the optimized heterostructure; it achieved a high photocurrent density of 11 µA/cm2 at 1.23 V bias vs. RHE and an applied bias photo-to-current efficiency of 4.1 × 10-3% at 0.76 V vs. RHE, as demonstrated by the photoelectrochemical measurements. These results underline the role of the two phases intermixing LFO and STO at the appropriate content to yield a high-performing photoanode ascribed to efficient charge separation and transfer. This suggests that LFO0.5/STO0.5 could be a potential candidate for the development of efficient photoanodes for hydrogen generation via photoelectrocatalytic water splitting.
RESUMO
Recently, green hydrogen production via solar thermochemical water splitting (STWS) as a clean and sustainable method is becoming a subject of interest to many researchers. Great efforts are being made to develop materials for STWS with suitable operating conditions, low cost, and good cycling stability. In this context, the study of mixed cobalt and nickel oxides with the general formula Co3-x Ni x O4 (0 ≤ x ≤ 1) was carried out, where four mixed metal oxides Co2.75Ni0.25O4, Co2.5Ni0.5O4, Co2.25Ni0.75O4, and Co2NiO4 have been successfully synthesized through the sol-gel method modified Pechini route. The structural investigation demonstrated that pure spinel structures were obtained for 0 ≤ x ≤ 0.75. A deep study was carried out with the main goal of finding the best phase that provides low redox temperature. Interesting reduction temperatures for all the compositions have been found, and the lowest values of 675 and 710 °C have been reported for Co2.25Ni0.75O4 and Co2.5Ni0.5O4, respectively. The thermal cycling results of this latest material using TGA measurement have proven attractive cycling stability of which the complete reoxidation of the samples was achieved. In addition, thermodynamic analysis of a reduction step was performed and good agreement of the theoretical reduction temperature of Co2.25Ni0.75O4 with the experimental one has been found.
RESUMO
Owing to their remarkable success in photocatalytic applications, multiferroic BiFeO3 and its derivatives have gained a highly promising position as electrode materials for future developments of efficient catalysts. In addition to their appropriate band gaps, these materials exhibit inherent intrinsic polarizations enabling efficient charge carrier separation and their high mobility without the need for additional co-catalysts. Here, we review the existing strategies for enhancing the photocatalytic performances of BiFeO3-based materials and we describe the physico-chemical properties at the origin of their exceptional photocatalytic behavior. A special focus is paid to the degradation of organic pollutants and water splitting, both driven through photocatalysis to unveil the correlation between BiFeO3 size, substitution, and doping on the one hand and the photocatalytic performances on the other hand. Finally, we provide practical recommendations for future developments of high-performing BiFeO3-based electrodes.
