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Enhancing corrosion resistance is essential for developing efficient electrocatalysts for acidic oxygen evolution reaction (OER). Herein, we report the strategic manipulation of the local compressive strain to reinforce the anti-corrosion properties of the non-precious Co3O4 support. The incorporation of Ru single atoms, larger in atomic size than Co, into the Co3O4 lattice (Ru-Co3O4), triggers localized strain compression and lattice distortion on the Co-O lattice. A comprehensive exploration of the correlation between this specific local compressive strain and electrocatalytic performance is conducted through experimental and theoretical analyses. The presence of the localized strain in Ru-Co3O4 is confirmed by operando X-ray absorption studies and supported by quantum calculations. This local strain, presented in a shortened Co-O bond length, enhances the anti-corrosion properties of Co3O4 by suppressing metal dissolutions. Consequently, Ru-Co3O4 shows satisfactory stability, maintaining OER for over 400 hours at 30 mA cm−2 with minimal decay. This study demonstrates the potential of the local strain effect in fortifying catalyst stability for acidic OER and beyond. Enhancing corrosion resistance is crucial for efficient electrocatalysts in the acidic oxygen evolution reaction. Here, the authors report the strategic manipulation of local compressive strain to improve the anti-corrosion properties of Co3O4, demonstrating stability for over 400 hours at 30 mA cm-2.
Zuo et al. (Mon,) studied this question.