Oct 2026· ChemSusChem· Vol 19 20· 0 citations· 98 references
Medicine
Abstract
Driven by the global imperative for carbon neutrality and sustainable energy development, oxygen electrocatalysis, especially the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR), has emerged as a key link between renewable electricity and clean energy conversion devices. However, the sluggish kinetics of these reactions severely limit energy efficiency, a challenge exacerbated by insufficient active-site utilization and restricted tri-phase mass transport. This review highlights recent advances in multiscale porous architectures for oxygen electrocatalysis, with particular emphasis on how pore size, connectivity, and hierarchical organization govern active-site accessibility, mass transport, and catalytic kinetics. Unlike previous reviews primarily centered on specific material categories, this work adopts a structure-function perspective to establish the correlations between porous architectures and electrocatalytic performance. Particular attention is given to d-band electronic-structure modulation and the confinement effects within hierarchically interconnected networks that expedite reactant diffusion. Finally, current challenges associated with structural stability under operating conditions, scalable fabrication, and operando mechanistic characterization are critically evaluated, and future perspectives for next-generation high-performance electrochemical devices are proposed to guide rational catalyst design.
Water electrolysis driven by renewable electricity is a promising route to clean hydrogen, but the anodic oxygen evolution reaction (OER) suffers from sluggish kinetics that limit the overall efficiency. Magnetite (Fe3O4) has emerged as an attractive non-noble-metal electrocatalyst for the oxygen evolution reaction, ow...
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The oxygen evolution reaction (OER) is a kinetically demanding anodic process in water electrolysis and related electrochemical energy-conversion systems. Its multistep proton-coupled electron-transfer kinetics and catalyst degradation under strongly oxidizing conditions limit overall efficiency and durability. High-en...
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Electrochemical energy conversion underpins the sustainable production of fuels and chemicals, with efficiency and selectivity governed by reactions at electrified solid-liquid interfaces. In supported electrocatalysts, metal-support interactions (MSIs) shape how catalytic states form and persist under polarization. Ye...
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Electrochemical water splitting enables renewable hydrogen production, yet laboratory catalyst activity often fails to translate into durable electrolyzer performance. This review integrates interfacial mechanisms, performance evaluation, degradation, and device requirements within a unified framework for the hydroge...
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Green hydrogen is a key energy vector for low-carbon transition, yet water electrolysis remains constrained by sluggish reaction kinetics and the high cost of noble-metal catalysts. High-entropy oxides (HEOs), which contain multiple metal cations, exhibit characteristic high-entropy, lattice-distortion, sluggish-diffus...
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Amid efforts toward carbon neutrality and rapid renewable energy development, CO2/CO electroreduction and water electrolysis have emerged as critical pathways for carbon resource recycling and green hydrogen production. However, CO2 and CO electroreduction reaction (CO2RR/CORR) remain limited by complex multielectron-t...
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