RESUMEN
The novel material class of high entropy oxides with their unique and unexpected physicochemical properties is a candidate for energy applications. Herein, it is reported for the first time about the physico- and (photo-) electrochemical properties of ordered mesoporous (CoNiCuZnMg)Fe2 O4 thin films synthesized by a soft-templating and dip-coating approach. The A-site high entropy ferrites (HEF) are composed of periodically ordered mesopores building a highly accessible inorganic nanoarchitecture with large specific surface areas. The mesoporous spinel HEF thin films are found to be phase-pure and crack-free on the meso- and macroscale. The formation of the spinel structure hosting six distinct cations is verified by X-ray-based characterization techniques. Photoelectron spectroscopy gives insight into the chemical state of the implemented transition metals supporting the structural characterization data. Applied as photoanode for photoelectrochemical water splitting, the HEFs are photostable over several hours but show only low photoconductivity owing to fast surface recombination, as evidenced by intensity-modulated photocurrent spectroscopy. When applied as oxygen evolution reaction electrocatalyst, the HEF thin films possess overpotentials of 420 mV at 10 mA cm-2 in 1 m KOH. The results imply that the increase of the compositional disorder enhances the electronic transport properties, which are beneficial for both energy applications.
RESUMEN
The demand for versatile and sustainable energy materials is on the rise, given the importance of developing novel clean technologies for transition to a net zero economy. Here, we present the synthesis, characterization, and application of lignin-derived ordered mesoporous carbons with various pore sizes (from 5 to approximately 50 nm) as anodes in sodium-ion batteries. We have varied the pore size using self-synthesized PEOn-b-PHAm block copolymers with different PEO and PHA chain lengths, applying the "soft templating" approach to introduce isolated spherical pores of 20 to 50 nm in diameters. The pore structure was evaluated by transmission electron microscopy (TEM), nitrogen physisorption, and small-angle X-ray scattering (SAXS). We report the microstructure analysis of such mesoporous lignin-based carbons using Raman spectroscopy and wide-angle X-ray scattering (WAXS). In comparison with nontemplated carbon and carbons templated employing commercial Pluronic F-127 and PIB50-b-PEO45, which created accessible channels and spherical pores up to approximately 10 nm in diameter, the carbon microstructure analysis revealed that templating with all applied polymers significantly impedes graphitization upon thermal treatment. Furthermore, the gained knowledge of similar carbon microstructures regardless of the type of template allowed the investigation of the influence of different pore morphologies in carbon applied as an anode material in sodium-ion batteries, supporting the previous theories in the literature that closed pores are beneficial for sodium storage while providing insights into the importance of pore size.