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Advances in dual-site mechanisms for designing high-performance oxygen evolution electrocatalysts

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November 1, 2025
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Enhanced Photocatalytic Efficiency Through Oxygen Vacancy‐Driven Molecular Epitaxial Growth of Metal–Organic Frameworks on BiVO 4

Abstract Efficient charge separation at the semiconductor/cocatalyst interface is crucial for high‐performance photoelectrodes, as it directly influences the ...

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Synergistic Atomic Environment Optimization of Nickel–Iron Dual Sites by Co Doping and Cr Vacancy for Electrocatalytic Oxygen Evolution

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Out-of-plane coordination of iridium single atoms with organic molecules and cobalt–iron hydroxides to boost oxygen evolution reaction

Abstract Advancements in single-atom-based catalysts are crucial for enhancing oxygen evolution reaction (OER) performance while reducing precious metal usage. A comprehensive understandi...

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Bulk polarization fields and interfacial electron sink in MXene-modified iodine-doped Bi4Ti3O12 enhance piezocatalytic H2O2 generation

Efforts to generate H2O2 through mechanical activation are hampered by poor charge control and low efficiency. Herein, a tailored catalyst strengthens internal fields and speeds reactions, markedly...

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What other academic literature is closely related to 'Advances in dual-site mechanisms for designing high-performance oxygen evolution electrocatalysts'?

Yes, highly correlated activity was mapped. An entry titled 'Enhanced Photocatalytic Efficiency Through Oxygen Vacancy‐Driven Molecular Epitaxial Growth of Metal–Organic Frameworks on BiVO 4' discusses this: Abstract Efficient charge separation at the semiconductor/cocatalyst interface is crucial for high‐performan...

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Yes, highly correlated activity was mapped. An entry titled 'Bulk polarization fields and interfacial electron sink in MXene-modified iodine-doped Bi4Ti3O12 enhance piezocatalytic H2O2 generation' discusses this: Efforts to generate H2O2 through mechanical activation are hampered by poor charge control and low efficiency. Herein, a tailored catalyst strength...

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