Journal of the American Chemical Society · 2025 · 35 citations · 65 references
Natural SciencesChemical EngineeringChemistryElectrochemistrySurface ChemistrySurface ScienceElectrochemical Energy ConversionElectrochemical SynthesisElectrode MaterialsRedox CatalysisRedox ChemistryWater OxidationCarbon ElectrodesChemical Process SynthesisElectric Double LayerElectrochemical OxidationElectrode FoulingHydrogen Peroxide GenerationHydrogen Peroxide SynthesisWork Function
Hydrogen peroxide (H 2 O 2 ) is an essential chemical for environmental remediation, chemical synthesis, and energy storage, yet conventional synthetic methods are energy-intensive and environmentally taxing. Herein, we report a catalyst-free strategy for H 2 O 2 synthesis by exploiting the gas–liquid–solid triple phase boundary formed at bubble-pinned porous carbon electrodes. The process involves three key mechanisms: (i) hydroxide anions enrichment in the electric double layer reduces the energy barrier for their oxidation to hydroxyl radicals, (ii) the hydrophobic bubble interface suppresses overoxidation, favoring the two-electron water oxidation pathway, and (iii) oxygen molecules capture electrons from previous steps to form H 2 O 2 . Density functional theory calculations indicate a 30% reduction in work function at the bubble-pinned interface compared to bubble-free counterparts, which thermodynamically promotes the electrochemical oxidation of hydroxide anions. Experiments verify that both water and oxygen are involved in H 2 O 2 generation, and mechanistic details are confirmed by trapping different radical intermediates. This study demonstrates an efficient and sustainable alternative for H 2 O 2 production, advancing interface-driven and catalyst-free chemistry.
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