Local compressive strain-induced anti-corrosion over isolated Ru-decorated Co<sub>3</sub>O<sub>4</sub> for efficient acidic oxygen evolution.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39496587.
- Also identified by DOI 10.1038/s41467-024-53763-8 and PMC identifier 11535344.
- Licence recorded as CC BY-NC-ND.
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Abstract
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 Co<sub>3</sub>O<sub>4</sub> support. The incorporation of Ru single atoms, larger in atomic size than Co, into the Co<sub>3</sub>O<sub>4</sub> lattice (Ru-Co<sub>3</sub>O<sub>4</sub>), 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-Co<sub>3</sub>O<sub>4</sub> 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 Co<sub>3</sub>O<sub>4</sub> by suppressing metal dissolutions. Consequently, Ru-Co<sub>3</sub>O<sub>4</sub> shows satisfactory stability, maintaining OER for over 400 hours at 30 mA cm<sup>-2</sup> with minimal decay. This study demonstrates the potential of the local strain effect in fortifying catalyst stability for acidic OER and beyond.