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Defect‐engineering is a viable strategy to improve the activity of nanocatalysts for the oxygen evolution reaction (OER), whose slow kinetics still strongly limits the broad market penetration of electrochemical water splitting as a sustainable technology for large‐scale hydrogen production. High‐entropy spinel oxides (HESOs) are in focus due to their great potential as low‐cost OER electrocatalysts. In this work, electrospun HESO nanofibers (NFs), based on (Cr,Mn,Fe,Co,Ni), (Cr,Mn,Fe,Co,Zn) and (Cr,Mn,Fe,Ni,Zn) combinations, with granular architecture and oxygen‐deficient surface are produced by calcination at low temperature (600 or 500 °C), characterized by a combination of benchtop analytical techniques and evaluated as electrocatalysts for OER in alkaline medium. The variation of HESO composition and calcination temperature produces complex and interdependent changes in the morphology of the fibers, crystallinity and inversion degree of the spinel oxide, concentration of the oxygen‐vacancies, cation distribution in the lattice, which mirror on different electrochemical properties of the fibers. The best electrocatalytic performance (overpotential and Tafel slope at 10 mA cm−2: 360 mV and 41 mV dec−1, respectively) pertains to (Cr1/5Mn1/5Fe1/5Co1/5Ni1/5)3O4 NFs calcined at 500 °C and results from the lower outer 3d‐electron number, eg filling closer to its optimal value and higher occupation of 16d sites by the most redox‐active species. [ABSTRACT FROM AUTHOR]

Perovskite-based solar cells are a promising photovoltaic technology capable of offering higher conversion efficiency at low costs compared with the standard of the market. They can be produced via a thin film technology that allows for considerable environmental sustainability, thus representing an efficient, sustainable, flexible, and light solution. Tandem solar cells represent the next step in the evolution of photovoltaics (PV). They promise higher power conversion efficiency (PCE) than those currently dominating the market. The tandem solar cell design overcomes the limitations of single junction solar cells by reducing the thermal losses as well as the manufacturing costs. Perovskite has been employed as a partner in different kinds of tandem solar cells, such as the Si and CIGS (copper indium gallium selenide) based cells that, in their tandem configuration with perovskite, can convert light more efficiently than standalone sub-cells. This brief review presents the main engineering and scientific challenges in the field. The state-of-the-art three main perovskite tandem technologies, namely perovskite/silicon, perovskite/CIGS, and perovskite/perovskite tandem solar cells, will be discussed, providing a side-by-side comparison of theoretical and experimental efficiencies of multijunction solar cells. [ABSTRACT FROM AUTHOR]

Zinc oxide with wide direct band gap and high exciton binding energy is one of the most promising materials for ultraviolet (UV) light-emitting devices. It further exhibits good performance in the degradation of non-biodegradable pollutants under UV irradiation. In this work, zinc oxide (ZnO) and zinc oxide/gold (ZnO/Au) nanocolloids are prepared by picosecond pulsed laser ablation (ps-PLA), using a Zn and Au metallic targets in water media at room temperature (RT) and 80°C. ZnO and Au nanoparticles (NPs) with size in the 10–50 nm range are obtained at RT, while ZnO nanorods (NRs) are formed when water is maintained at 80°C during the ps-PLA process. Au NPs, added to ZnO colloids after the ablation process, decorate ZnO NRs. The crystalline phase of all ZnO nanocolloids is wurtzite. Methylene blue dye is used to investigate the photo-catalytic activity of all the synthesised nanocolloids, under UV light irradiation.

High-entropy oxide nanofibers, based on equimolar (Cr,Mn,Fe,Co,Ni), (Cr,Mn,Fe,Co,Zn) and (Cr,Mn,Fe,Ni,Zn) combinations, were prepared by electrospinning followed by calcination. The obtained hollow nanofibers exhibited a porous structure consisting of interconnected nearly strain-free (Cr1/5Mn1/5Fe1/5Co1/5Ni1/5)3O4, (Cr1/5Mn1/5Fe1/5Co1/5Zn1/5)3O4 and (Cr1/5Mn1/5Fe1/5Ni1/5Zn1/5)3O4 single crystals with a pure Fd3¯m spinel structure. Oxidation state of the cations at the nanofiber surface was assessed by X-ray photoelectron spectroscopy and cation distributions were proposed satisfying electroneutrality and optimizing octahedral stabilization. The magnetic data are consistent with a distribution of cations that satisfies the energetic preferences for octahedral vs. tetrahedral sites and is random only within the octahedral and tetrahedral sublattices. The nanofibers are ferrimagnets with relatively low critical temperature more similar to cubic chromites and manganites than to ferrites. Replacing the magnetic cations Co or Ni with non-magnetic Zn lowers the critical temperature from 374 K (Cr,Mn,Fe,Co,Ni) to 233 and 105 K for (Cr,Mn,Fe,Ni,Zn) and (Cr,Mn,Fe,Co,Zn), respectively. The latter nanofibers additionally have a low temperature transition to a reentrant spin-glass-like state. [ABSTRACT FROM AUTHOR]

Entropy‐stabilized oxides (ESOs), such as (Mg0.2Co0.2Ni0.2Cu0.2Zn0.2)O, have recently gained significant interest as novel anodes for lithium‐ion batteries (LIBs) due to their stable crystal structure and robust lithium‐storage properties. In this work, (Mg0.2Co0.2Ni0.2Cu0.2Zn0.2)O oxides with different morphologies are prepared by electrospinning and solvothermal method and are applied as anode active materials for LIBs. It is found that different morphologies possess different characteristics, namely particle size, particle size range, and defect density, which have a significant effect on the electrochemical behavior. The most active (Mg, Co, Ni, Cu, Zn) ESO shows outstanding electrochemical properties in terms of high reversible capacity (480 mAh g–1 at 20 mA g–1), superior rate capability (206 mAh g–1 at 2 A g–1), and excellent cycling stability (390 mAh g–1 at 500 mA g–1 after 300 cycles). The strategy demonstrates the importance of engineering microstructures in tailoring the electrochemical performance. [ABSTRACT FROM AUTHOR]