Sol-Gel Synthesis of Ceria-Zirconia-Based High-Entropy Oxides as High-Promotion Catalysts for the Synthesis of 1,2-Diketones from Aldehyde

Efficient Lewis-acid-catalyzed direct conversion of aldehydes to 1,2-diketones in the liquid phase was enabled by using newly designed and developed ceria–zirconia-based high-entropy oxides (HEOs) as the actual catalysts. The synergistic effect of various cations incorporated in the same oxide structure (framework) was partially responsible for the efficiency of multicationic materials compared to the corresponding single-cation oxide forms. Furthermore, a clear, linear relationship between the Lewis acidity and the catalytic activity of the HEOs was observed. Due to the developed strategy, exclusively diketone-selective, recyclable, versatile heterogeneous catalytic transformation of aldehydes can be realized under mild reaction conditions

Resolving a structural issue in cerium-nickel-based oxide

CeNiO3 has been reported in the literature in the last few years as a novel LnNiO3 compound with promising applications in different catalytic fields, but its structure has not been correctly reported so far. In this research, CeNiO3 (RB1), CeO2 and NiO have been synthesized in a nanocrystalline form using a modified citrate aqueous sol-gel route. A direct comparison between the equimolar physical mixture (n(CeO2) : n(NiO) = 1:1) and a compound RB1 was made. Their structural differences were investigated by laboratory powder X-ray diffraction (PXRD), selected area electron diffraction (SAED), transmission electron microscopy (TEM) with energy-dispersive X-ray spectroscopy detector (EDS), and Raman spectroscopy. The surface of the compounds was analyzed by X-ray photoelectron spectroscopy (XPS), while the thermal behaviour was explored by thermogravimetric analysis (TGA). Their magnetic properties were also investigated with the aim of exploring the differences between these two compounds. There were clear differences between the physical mixture of CeO2 + NiO and RB1 presented by all of these employed methods. Synchrotron methods, such as atomic pair distribution function analysis (PDF), X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) were used to explore the structure of RB1 in more detail. Three different models for the structural solution of RB1 were proposed. One structural solution proposes that RB1 is a single-phase pyrochlore compound (Ce2Ni2O7) while the other two solutions suggest that RB1 is a two-phase system of either CeO2 + NiO or Ce1–xNixO2 and NiO

B = W, Te) with ferromagnetic and dielectric properties for triboelectric energy harvesting

Four iron-based triple tungstate and tellurate perovskites have been synthesized in the nanocrystalline form using a simple sol–gel citrate route: Sr3Fe2WO9 (SFWO), Ba3Fe2WO9 (BFWO), Sr3Fe2TeO9 (SFTO), and Ba3Fe2TeO9 (BFTO). Strontium-based compounds crystallize in the tetragonal space group I4/m, while barium-based compounds crystallize in the hexagonal space group P63/mmc. All compounds possess a ferromagnetic order with high values for room-temperature magnetization. The magnetic state as traced by Mo¨ssbauer spectroscopy is heterogeneously related to disorder. The compounds also possess relatively high dielectric constants (20–199.16) measured at 1 MHz and a moderate loss factor. The synthesized triple perovskite compounds were utilized in the fabrication of vertical contact mode triboelectric nanogenerators (TENGs). The working mechanism and the electrical response of the TENGs were extensively studied. The TENG device based on BFTO/Kapton triboelectric layers produces the highest output of 88 V/2.69 mA. For the first time, the surface polarity of the triple perovskite was shown using a Kelvin probe force microscopy technique (KPFM), which elucidates the positive polarity of the triboelectric layer. Furthermore, the TENG device was used to charge several capacitors and to carry out the powering of electronics that make it an excellent choice for various self-powered applications

Sol-Gel Synthesis of Ceria-Zirconia-Based High-Entropy Oxides as High-Promotion Catalysts for the Synthesis of 1,2-Diketones from Aldehyde

Efficient Lewis-acid-catalyzed direct conversion of aldehydes to 1,2-diketones in the liquid phase was enabled by using newly designed and developed ceria–zirconia-based high-entropy oxides (HEOs) as the actual catalysts. The synergistic effect of various cations incorporated in the same oxide structure (framework) was partially responsible for the efficiency of multicationic materials compared to the corresponding single-cation oxide forms. Furthermore, a clear, linear relationship between the Lewis acidity and the catalytic activity of the HEOs was observed. Due to the developed strategy, exclusively diketone-selective, recyclable, versatile heterogeneous catalytic transformation of aldehydes can be realized under mild reaction conditions