Achieving scalable fabrication of robust and uniform single-atom catalyst-based gas-diffusion electrodes (SAC-GDEs) remains challenging. Here, a universal one-step soot-deposition route was developed to convert various metal-containing paraffins into conformal single-atom catalyst (SAC) coatings on diverse electrodes (1D fibers, 2D plates, and 3D foams). The process provides multiscale control, from precursor-defined molecular coordination to micropore wettability and macroscopic geometry, to collectively engineer hierarchical coating films that couple intensified mass transfer and high intrinsic catalytic activity for efficient H₂O₂ electrosynthesis. As a device-level demonstration, Pd-SAC-GDE delivers pH-universal H₂O₂ production under an industrial-level current (500 mA cm⁻²) for 100 h, achieving a record-high H₂O₂ yield of 16.9 mol g⁻¹ h⁻¹. A tip-enhanced mechanism was proposed based on constant-potential calculations. The results reveal that the curvature-enhanced localized electric field promotes O₂ polarization and activation at the Pd-O₃ sites, thereby facilitating both *OOH generation and adsorption and ultimately leading to highly selective H₂O₂ production. This facile, broadly applicable fabrication strategy significantly advances the scalable manufacture of SAC-coated GDEs for environmental and sustainable catalysis.
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Li et al. (2026) studied this question.
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