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Using electrocatalytic water reduction to produce hydrogen fuel offers significant potential for clean energy, yet its large-scale adoption depends on developing cost-effective, non-precious, and efficient catalysts to replace expensive Pt-based state-of-the-art HER catalysts. The catalytic HER performance of an active catalyst largely depends on the available catalytic active sites, conductivity, and intrinsic electrochemical kinetics, all of which can be altered by incorporating a heteroatom into the active catalyst structure. Herein, we synthesized a unique nitrogen-doped CuO@CuS (NCOS) core–shell-structured catalyst through a facile hydrothermal process followed by an efficacious nitrogenation process, and its electrochemical performance for the HER was systematically analyzed. The NCOS core–shell-structured catalyst exhibits a reduced overpotential (55 mV) and Tafel slope (107 mV dec−1) compared to the pure CuS (CS; 179 mV and 201 mV dec−1) catalyst at a current density of 10 mA cm−2. Moreover, the NCOS core–shell-structured catalyst demonstrates excellent endurance for up to 50 h of chronopotentiometric testing at a driving current density rate of 10 and 100 mA cm−2. This excellent catalytic HER activity is a result of an increased electron transfer rate and a greater number of accessible active sites, attributed to a change in structural properties and the high electronic conductivity aroused from nitrogen incorporation, as evidenced from the TOF and EIS curve analyses. [ABSTRACT FROM AUTHOR]

Silicon belongs to group 14 elements along with carbon, germanium, tin, and lead in the periodic table. Similar to carbon, silicon is capable of forming a wide range of stable compounds, including silicon hydrides, organosilicons, silicic acids, silicon oxides, and silicone polymers. These materials have been used extensively in optoelectronic devices, sensing, catalysis, and biomedical applications. In recent years, silicon compounds have also been shown to be suitable for stabilizing delicate halide perovskite structures. These composite materials are now receiving a lot of interest for their potential use in various real‐world applications. Despite exhibiting outstanding performance in various optoelectronic devices, halide perovskites are susceptible to breakdown in the presence of moisture, oxygen, heat, and UV light. Silicon compounds are thought to be excellent materials for improving both halide perovskite stability and the performance of perovskite‐based optoelectronic devices. In this work, a wide range of silicon compounds that have been used in halide perovskite research and their applications in various fields are discussed. The interfacial stability, structure–property correlations, and various application aspects of perovskite and silicon compounds are also analyzed at the molecular level. This study also explores the developments, difficulties, and potential future directions associated with the synthesis and application of perovskite‐silicon compounds. [ABSTRACT FROM AUTHOR]

The deprived electrochemical kinetics of the oxygen evolution reaction (OER) catalyst is the prime bottleneck and remains the major obstacle in the water electrolysis processes. Herein, a facile hydrothermal technique was implemented to form a freestanding polyhedron-like Co3O4 on the microporous architecture of Ni foam, its reaction kinetics enhanced through sulfide counterpart transformation in the presence of Na2S, and their catalytic OER performances comparatively investigated in 1 M KOH medium. The formed Co3S4 catalyst shows outstanding catalytic OER activity at a current density of 100 mA cm−2 by achieving a relatively low overpotential of 292 mV compared to the pure Co3O4 catalyst and the commercial IrO2 catalyst. This enhancement results from the improved active centers and conductivity, which boost the intrinsic reaction kinetics. Further, the optimized Co3S4 catalyst exhibits admirable prolonged durability up to 72 h at varied current rates with insignificant selectivity decay. The energy dispersive X-ray spectroscopy (EDX) and Raman spectra measured after the prolonged OER stability test reveal a partial transformation of the active catalyst into an oxyhydroxide phase (i.e., CoOOH@Co3S4), which acts as an active catalyst phase during the electrolysis process. [ABSTRACT FROM AUTHOR]

Developing effective and long-lasting electrocatalysts for oxygen evolution reaction (OER) is critical for increasing sustainable hydrogen production. This paper describes the production and characterization of CoFeP nanoparticles (CFP NPs) as high-performance electrocatalysts for OER. The CFP NPs were produced using a simple hydrothermal technique followed by phosphorization, yielding an amorphous/crystalline composite structure with improved electrochemical characteristics. Our results reveal that CFP NPs have a surprisingly low overpotential of 284 mV at a current density of 100 mA cm−2, greatly exceeding the precursor CoFe oxide/hydroxide (CFO NPs) and the commercial RuO2 catalyst. Furthermore, CFP NPs demonstrate exceptional stability, retaining a constant performance after 70 h of continuous operation. Post-OER characterization analysis revealed transformations in the catalyst, including the formation of cobalt–iron oxides/oxyhydroxides. Despite these changes, CFP NPs showed superior long-term stability compared to native metal oxides/oxyhydroxides, likely due to enhanced surface roughness and increased active sites. This study proposes a viable strategy for designing low-cost, non-precious metal-based OER catalysts, which will help advance sustainable energy technology. [ABSTRACT FROM AUTHOR]

Water electrolysis is a highly efficient route to produce ideally clean H2 fuel with excellent energy conversion efficiency and high gravimetric energy density, without producing carbon traces, unlike steam methane reforming, and it resolves the issues of environmental contamination via replacing the conventional fossil fuel. Particular importance lies in the advancement of highly effective non-precious catalysts for the oxygen evolution reaction (OER). The electrocatalytic activity of an active catalyst mainly depends on the material conductivity, accessible catalytically active sites, and intrinsic OER reaction kinetics, which can be tuned via introducing N heteroatoms in the catalyst structure. Herein, the efficacious nitrogenation of CuS was accomplished, synthesized using a hydrothermal procedure, and characterized for its electrocatalytic activity towards OER. The nitrogen-doped CuO@CuS (N,CuO@CuS) electrocatalyst exhibited superior OER activity compared to pristine CuS (268 and 602 mV), achieving a low overpotential of 240 and 392 mV at a current density of 10 and 100 mA/cm2, respectively, ascribed to the favorable electronic structural modification triggered by nitrogen incorporation. The N,CuO@CuS also exhibits excellent endurance under varied current rates and a static potential response over 25 h with stability measured at 10 and 100 mA/cm2. [ABSTRACT FROM AUTHOR]