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 |
J Colloid Interface Sci
January 2025
School of Materials Science and Engineering, Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, PR China. Electronic address:
The development of earth-abundant oxygen evolution reaction (OER) electrocatalysts with high activity and durability is critical for replacing noble-metal-based catalysts in the applications of scalable water electrolysis. A freestanding electrode architecture offers significant advantages over conventional coated powder forms due to enhanced kinetics and stability. However, precise control over electrode composition and the construction of uniformly distributed active sites within these electrodes remain challenging.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Materials Science and Engineering, National University of Singapore, Singapore 117575, Singapore.
Electrochemical water splitting is a promising method for generating green hydrogen gas, offering a sustainable approach to addressing global energy challenges. However, the sluggish kinetics of the anodic oxygen evolution reaction (OER) poses a great obstacle to its practical application. Recently, increasing attention has been focused on introducing various external stimuli to modify the OER process.
View Article and Find Full Text PDFInorg Chem
January 2025
Key Laboratory of Polymer Materials of Gansu Province, Key Laboratory of Eco-functional Polymer Materials of the Ministry of Education, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070, Gansu, China.
Efficient and stable nonprecious metal-based oxygen evolution reaction (OER) electrocatalysts are pivotal for water electrolysis technology. Herein, we are reporting an effective strategy for fabricating efficient Co-based OER electrocatalysts by low-level Fe doping in CoMoO to boost surface reconstruction and electronic modulation, which resulted in excellent OER electroactivity consequently. Our findings reveal that a mere 5.
View Article and Find Full Text PDFNanoscale Adv
January 2025
Department of Chemistry, Quaid-i-Azam University Islamabad-45320 Pakistan
Research on water splitting is paramount for developing low-carbon alternative energy sources. Nevertheless, creating an efficient, cost-effective, and bifunctional electrocatalyst that facilitates both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) remains an elusive goal. In this work, we report a novel hybrid nanostructured electrocatalyst by combining and pyrolyzing MXene, MIL-53(Fe), and ZIF-67.
View Article and Find Full Text PDFSci Rep
January 2025
Hangzhou Yanqu Information Technology Co., Ltd., Hangzhou, 310003, Zhejiang, China.
Electrocatalytic materials with dual functions of oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) have received increasing attention in the field of zinc-air batteries (ZABs) research. In this study, bifunctional CoNC@NCXS catalysts were prepared by anchoring Co and N co-doped CoNC on N-doped carbon xerogel sphere (NCXS) based on the spatially confined domain effect and in-situ doping technique. CoNC@NCXS exhibited excellent ORR/OER activity in alkaline electrolytes with the ORR onset potential of 0.
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