98%
921
2 minutes
20
Low voltage driven overall water splitting remains a significant challenge for practical hydrogen production. The unique interface and interaction between different components in heterostructures endow them with extraordinary properties that are not achievable in single-component materials. In this study, we introduce the NiP-FeP heterostructure as a catalyst for the oxygen evolution reaction (OER) to enable efficient overall water splitting. In 1 M KOH solution, the NiP-FeP electrocatalysts required overpotentials of 246.2 mV for OER to deliver the current density of 100 mA cm. This outstanding catalytic activity can be attributed to the well-defined heterointerfaces that effectively activate reaction intermediates, the high electrical conductivity of the phosphide components for rapid electron transfer, and the favorable structure that promotes efficient mass transport. Moreover, the NiP-FeP electrocatalysts show great potential for practical applications as it maintains remarkable durability over 24 h of continuous operation in alkaline simulated seawater. These results suggest that NiP-FeP could serve as a promising candidate for OER, particularly in practical applications like seawater electrolysis, where durability and low overpotential are crucial for sustainable hydrogen production.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.langmuir.5c01501 | DOI Listing |
ACS Nano
September 2025
Eastern Institute for Advanced Study, Eastern Institute of Technology, Ningbo, Zhejiang 315200, P. R. China.
Ni-Fe (oxy)hydroxides are among the most active oxygen evolution reaction (OER) catalysts in alkaline media. However, achieving precise control over local asymmetric Fe-O-Ni active sites in Ni-Fe oxyhydroxides for key oxygenated intermediates' adsorption steric configuration regulation of the OER is still challenging. Herein, we report a two-step dealloying strategy to fabricate asymmetric Fe-O-Ni pair sites in the shell of NiOOH@FeOOH/NiOOH heterostructures from NiFe Prussian blue analogue (PBA) nanocubes, involving anion exchange and structure reconstruction.
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 Commun (Camb)
September 2025
State Key Laboratory of New Textile Materials & Advanced Processing Technology, College of Materials Science and Engineering, Wuhan Textile University, Wuhan, 430200, China.
The faradaic efficiency of the electro-synthesis of ammonia using the nitrate reduction reaction (NORR) relies on an electrocatalyst to hydrogenate NO and simultaneously suppress the hydrogen evolution reaction (HER). Due to the formation of a heterostructure, the faradaic efficiency of g-CN/BiO reaches 91.12% at -0.
View Article and Find Full Text PDFNat Prod Rep
September 2025
Royal Botanic Gardens Kew, Richmond, London, TW9 3AE, UK.
Covering upto 2025Rotenoids are angular hybrid isoflavonoids mainly characterized by an additional six-membered ring between the B and C rings of flavonoids. The extra ring introduces further chemical diversity to the densely substituted precursors, isoflavonoids, making rotenoids a significant group of compounds within the plant kingdom. Early biosynthesis studies by L.
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
Department of Electrical and Computer Engineering, University of Houston, Houston, Texas 77204, United States.
The development of efficient and economical oxygen evolution reaction (OER) catalysts is highly desired, and cobalt-based nanomaterials are promising candidates. In this work, we tackle one key question for cobalt-assisted photocatalytic OER: What is the true active species of Co(OH) for the photocatalytic OER? Hence, we investigated photocatalytic OER on nanostructured Co(OH) and CoO for comparison. We found that there was a significant transformation of Co(OH) during the photocatalytic process with a [Ru(bpy)]/SO buffer.
View Article and Find Full Text PDF