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Supported metal catalysts with appropriate metal-support interactions (MSIs) hold a great promise for heterogeneous catalysis. However, ensuring tight immobilization of metal clusters/nanoparticles on the support while maximizing the exposure of surface active sites remains a huge challenge. Herein, we report an Ir/WO catalyst with a new enrooted-type MSI in which Ir clusters are, unprecedentedly, atomically enrooted into the WO lattice. The enrooted Ir atoms decrease the electron density of the constructed interface compared to the adhered (root-free) type, thereby achieving appropriate adsorption toward oxygen intermediates, ultimately leading to high activity and stability for oxygen evolution in acidic media. Importantly, this work provides a new enrooted-type supported metal catalyst, which endows suitable MSI and maximizes the exposure of surface active sites in contrast to the conventional adhered, embedded, and encapsulated types.
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http://dx.doi.org/10.1002/anie.202406947 | 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.
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