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The rational design of economical and highly active multifunctional electrocatalysts is urgently needed for producing sustainable hydrogen. Here, we introduce a novel heterostructured electrocatalyst (NFM) by integrating NiCoO and FeCoS with MoTiCT-MXene nanosheets on a nickel foam substrate for the robust electrocatalytic water splitting and urea oxidation. Notably, the optimized NFM electrocatalyst achieves an impressive activity, requiring ultra-low overpotentials of 58.2, 190.3 mV for the hydrogen evolution reaction (HER) and 182.4, 241.5 mV for the oxygen evolution reaction (OER) to reach current rates of 10 and 100 mA cm, respectively, in 1 M KOH. When utilized as both the anode and cathode in a full water electrolyzer, NFM achieves a cell voltage of only 1.52 V at 10 mA cm and exhibits long-term durability over 100 h at 100 mA cm, outperforming many conventional electrolyzer systems. Finally, in the context of urea electrolysis, the NFM catalyst operates at a low potential of 1.40 V to achieve 100 mA cm, showcasing its multifunctional capabilities. Density functional theory calculations verify that the rich heterointerfaces within the NFM catalyst facilitates interfacial electron transport, leading to an enhancement in intermediate adsorption and reducing the energy barrier for the HER/OER. More importantly, the synergistic interaction at these nanointerfaces modulates electron density around the active sites, unlocking its potential for use in high-performance electrocatalytic applications.
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http://dx.doi.org/10.1016/j.jcis.2025.138426 | DOI Listing |
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September 2025
School of Photovoltaic and Renewable Energy Engineering, University of New South Wales, Sydney, 2052, Australia.
Plastic waste continues to be a major environmental challenge, worsened by energy-intensive conventional recycling methods that require highly pure feedstocks. In this review, emerging electrochemical upcycling technologies are critically examined, focusing on the electro-oxidation transformation of polyethylene terephthalate (PET) into valuable chemical products. Key reaction pathways and target products are outlined to clarify the selective electrochemical reforming of PET.
View Article and Find Full Text PDFNat Chem
September 2025
Department of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.
Proton transfer plays an important role in both hydrogen and oxygen evolution reactions during electrocatalytic water splitting to produce green hydrogen. However, directly adapting the conventional proton/deuterium kinetic isotope effect to study proton transfer in heterogeneous electrocatalytic processes is challenging. Here we propose using the shift in the Tafel slope between protic and deuteric electrolytes, or the Tafel slope isotope effect, as an effective probe of proton transfer characteristics.
View Article and Find Full Text PDFDalton Trans
September 2025
Sun Yat-Sen University, MOE Laboratory of Polymeric Composite and Functional Materials, School of Materials Science and Engineering, Guangzhou 510275, China.
The main bottleneck faced by traditional hydrogen production technology through water electrolysis lies in the high energy consumption of the anodic oxygen evolution reaction (OER). Combining the thermodynamically favorable ethanol oxidation reaction (EOR) with the hydrogen evolution reaction provides a promising route to reduce the energy consumption of hydrogen production and generate high value-added products. In this study, a facile method was developed for nickel oxyhydroxide (NiOOH) fabrication.
View Article and Find Full Text PDFChem Asian J
September 2025
School of Medical Information Engineering, Shenyang Medical College, Shenyang, Liaoning, 110043, P. R. China.
The rational design of electrode materials with outstanding energy and power density for supercapacitors (SCc) and high-performance electrocatalysts in alkaline media plays an indispensable role in the application of energy storage and overall water splitting. In this paper, we prepared NiCoFe layered ternary hydroxides (LTH) using a hydrothermal synthesis method. The sample with a Ni/Co/Fe ratio of 1:2:0.
View Article and Find Full Text PDFChemistry
September 2025
Department of Molecular Theory and Spectroscopy, Max-Planck-Institut für Kohlenforschung, 45470, Mülheim an der Ruhr, Germany.
In this study, we seek to deepen the understanding of the Fe effect in Ni-oxyhydroxide-mediated oxygen evolution reaction (OER) electrocatalysis in alkaline conditions, where extremely small amounts of Fe can have a dramatic impact on catalytic performance. For this purpose, Density Functional Theory (DFT) electronic structure calculations with implicit solvation description is employed in a constant pH/potential simulation framework. Nanoparticle models are considered for the nickel-based oxyhydroxide material with different degrees of Fe incorporation, and the pH/U-dependent interface structure is studied.
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