Breathing mode in Nd-CoO<sub>x</sub> for active and stable proton exchange membrane water electrolysis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41365880.
- Also identified by DOI 10.1038/s41467-025-66408-1 and PMC identifier 12689798.
- Licence recorded as CC BY-NC-ND.
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Abstract
Proton-exchange membrane water electrolysis in acidic solutions holds great promise for advancing the green-hydrogen economy but limited by using precious-metal catalysts. Here, we develop a low-cost Co<sub>3</sub>O<sub>4</sub>-based catalyst with oxygen vacancies and Nd-insertion (Nd-CoO<sub>x</sub>). This catalyst achieves a low overpotential of 317 mV at 10 mA cm<sup>-2</sup> for acidic oxygen evolution reaction and remains stable over 800 h. The oxygen vacancies in Nd-CoO<sub>x</sub> enhance its catalytic activity, while Nd enables the long-term stability through a flexible "breathing mode" during oxygen evolution reaction, as revealed by in-situ methods such as X-ray absorption spectroscopy and Raman spectroscopy. The presence of Nd also improves the catalytic activity with the oxide path mechanism. This favorable strategy can be extended to other lanthanides. When used as the anode, Nd-CoO<sub>x</sub> delivers good performance in water electrolysis to achieve 200 mA cm<sup>-2</sup> at a low cell voltage of 1.69 V with low degradation over 100 h, and can reach 1 and 2 A cm<sup>-2</sup> at 1.93 V and 2.12 V, respectively.