The amount of active sites of a catalyst is of great importance to enhance the oxygen evolution reaction (OER) activity. Here, the sheet-on-sheet strategy is proposed to effectively increase the density of active sites of NiFe layered double hydroxide (NiFe LDH) catalyst in terms of structural engineering. As a non-precious electrocatalyst for the OER, NiFe LDH is grown directly on CuO nanosheets. As a result, the received NiFe LDH/CuO nanosheet catalyst with sheet-on-sheet structure shows an ultralow overpotential of 270 mV at 20 mA cm, much lower than that of RuO as a benchmark. The CuO nanosheets, as substrate, play the vital role in downsizing the NiFe LDH, leading to the raised active site density.
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http://dx.doi.org/10.1039/d0ra02985h | DOI Listing |
Chem Commun (Camb)
January 2025
Fujian Provincial Key Laboratory of Polymer Materials, College of Materials Science and Engineering, Fujian Normal University, Fuzhou 350007, China.
In this study, the NiFe-LDH doped with different Pt group metals (Pt, Ru, Ir, Rh) was prepared as a cocatalyst for photocatalytic H production over g-CN. It is found that the doped NiFe-LDH loaded g-CN generally displays higher photocatalytic activity than the raw NiFe-LDH modified one, where the NiFeRu-LDH loaded g-CN shows the optimal H evolution rate of 77.4 μmol h, about 5.
View Article and Find Full Text PDFSmall
January 2025
College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan, Shandong, 250014, China.
Renewable energy-powered seawater electrolysis is a green and attractive technique for producing high-purity hydrogen. However, severe chlorideions (Cl) and their derivatives tend to corrode anodic catalysts at ampere-level current densities and hinder the application of seawater-to-H systems. Herein, a polycalmagite (PCM)-coated NiFe layered double hydroxide is presented on Ni foam (NiFe LDH@PCM/NF) that exhibits exceptional stability in alkaline seawater.
View Article and Find Full Text PDFDalton Trans
January 2025
School of Materials and Chemistry, University of Shanghai for Science and Technology, Jungong Road 334#, 200093 Shanghai, China.
Recently, photo-assisted electrocatalysis as an emerging catalytic approach that combines the technologies of photocatalysis and electrocatalysis has attracted great interest among researchers. Under this circumstance, the NiFe-LDH compounded with PbS based (PbS@NFHS) heterojunction with both photoactive and electrocatalytic properties was constructed for the first time through an ambient etching route and a subsequent low-temperature hydrothermal method. The as-prepared catalyst displayed a novel hierarchical 3D open structure based on nanosheets, which offered numerous electrochemically active sites, facilitated the swift diffusion of ions and enhanced both electrical conductivity and catalytic stability, thus significantly improving the catalytic performance.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan 250014 Shandong, China; Center for High Altitude Medicine, West China Hospital, Sichuan University, Chengdu 610041 Sichuan, China. Electronic address:
Seawater splitting is increasingly recognized as a promising technique for hydrogen production, while the lack of good electrocatalysts and detrimental chlorine chemistry may hinder further development of this technology. Here, the interfacial engineering of manganese dioxide nanoparticles decorated on NiFe layered double hydroxide supported on nickel foam (MnO@NiFe LDH/NF) is reported, which works as a robust catalyst for alkaline seawater oxidation. Density functional theory calculations and experiment findings reveal that MnO@NiFe LDH/NF can selectively enrich OH and repel Cl in oxygen evolution reaction (OER).
View Article and Find Full Text PDFNat Commun
January 2025
National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, PR China.
Transition-metal layered double hydroxides are widely utilized as electrocatalysts for the oxygen evolution reaction (OER), undergoing dynamic transformation into active oxyhydroxides during electrochemical operation. Nonetheless, our understanding of the non-equilibrium structural changes that occur during this process remains limited. In this study, utilizing in situ energy-dispersive X-ray absorption spectroscopy and machine learning analysis, we reveal the occurrence of deprotonation and elucidate the role of incorporated iron in facilitating the transition from nickel-iron layered double hydroxide (NiFe LDH) into its active oxyhydroxide.
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