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The transition metal-based catalysts have great potential to boost the electrocatalytic reactions due to their flexible electronic configuration and low cost. This work developed a facile emulsion aggregation strategy to synthesize coral-like carbon-wrapped NiCo alloy (CoNi/rGO) with high oxygen evolution reaction (OER) activity. The effect of alloy composition and GO content on the OER activity was evaluated in the 1 mol L KOH solution. The OER mechanism of the CoNi/rGO catalyst was disclosed by X-ray photoelectron spectra (XPS) and synchrotron radiation X-ray absorption spectra (XAS). The emulsion containing amphipathic graphene oxide (GO) and hydrophobic nickel/cobalt complexes induces the formation of the carbon-wrapped nanostructure. The coral-like CoNi/rGO catalyst exhibits the low overpotential of 288 mV at the current density of 10 mA cm and good durability, both of which are superior to the standard RuO. The synergistic effect between nickel and cobalt effectively regulates the electronic structure and OER activity of the alloy catalysts. Moreover, the interaction between NiCo alloys and carbon shells can reduce the interfacial resistance.
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http://dx.doi.org/10.1016/j.jcis.2020.03.124 | DOI Listing |
Langmuir
September 2025
College of Materials Science and Engineering, North University of China, Taiyuan 030051, PR China.
The oxygen evolution reaction (OER), a critical yet kinetically sluggish process in electrochemical water splitting, severely limits efficient hydrogen production. Herein, a simple one-step dynamic hydrogen bubble templated electrodeposition technique is used to prepare a self-supported 3D porous NiCuFeP catalyst with outstanding OER performance. In 1.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Strategic Research Center for Smart Battery, Korea Basic Science Institute (KBSI), Daejeon 34133, Republic of Korea. Electronic address:
Advancing impactful, economical, and durable Co-based bifunctional electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) has been crucial in developing sustainable energy technologies. In this work, Co and CoN nanoparticles (NPs)-incorporated S, N-doped carbon catalysts (Co/CoN/SNC) were prepared via direct pyrolysis of the CoDATT complex, exhibiting high bifunctional electrocatalytic performance for ORR and OER. The complex precursor, CoDATT, was synthesized for the first time using diaminoterthiophene (DATT) and CoCl.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Chemical and Materials Engineering, National Yunlin University of Science and Technology, 123 University Road, Section 3, Douliou, Yunlin 64002, Taiwan.
Urea electrolysis holds tremendous promise to remediate urea-containing wastewater and produce cost-effective hydrogen. Achieving highly efficient and durable electrocatalysts to drive the anodic urea oxidation reaction (UOR) is paramount to promote its practical applications. Herein, electroless deposition, a scalable, cost-effective, and energy-saving approach, is used to obtain amorphous Ni-Co-P nanoparticles.
View Article and Find Full Text PDFNanoscale
September 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, Jiangsu, China.
Proton exchange membrane water electrolysis (PEMWE) is regarded as the most promising technique for the sustainable production of green hydrogen due to its multiple advantages such as high working current density and high hydrogen purity. However, the anodic oxygen evolution reaction (OER) has a significant impact on the overall efficiency of the electrolytic water reaction due to its sluggish kinetics, which has prompted the search for catalysts possessing both high activity and durability. Iridium oxide exhibits excellent stability under acidic conditions but has poor catalytic activity, leading to its inability to meet the strict requirements of large-scale industrial applications.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan 430074, China.
The lattice oxygen mechanism (LOM) of the oxygen evolution reaction (OER) offers significant kinetic advantages over the adsorbed oxygen mechanism. Anion intercalation induces the LOM in NiOOH by enhancing the covalency of lattice oxygen through the modulation of the metal-oxygen electronic state. The relationships between doping mechanisms, such as the size and valence state of anions and the kinetics of the OER, have been clarified.
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