Ten thousand hour stable zinc air batteries via Fe and W dual atom sites.
basic_science · Level V
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- Record sourced from PubMed, PMID 40883304.
- Also identified by DOI 10.1038/s41467-025-63540-w and PMC identifier 12397402.
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Abstract
Durable and highly active oxygen electrocatalysts are crucial to the large-scale application of rechargeable zinc-air batteries. Here we utilize the N<sub>4</sub> unit in phthalocyanine molecule to trap the tungsten atoms scratched off from the tungsten carbide milling balls and place the obtained W-N<sub>4</sub> unit adjacent to the Fe-N<sub>4</sub> units from iron (Ⅱ) phthalocyanine, resulting in highly active Fe-N<sub>4</sub>/W-N<sub>4</sub> diatomic sites with well-pronounced 3d-5d hybrid for efficient and durable oxygen electrocatalysis. The electron distribution of the Fe-N<sub>4</sub> site is optimized by the neighboring W-N<sub>4</sub> site, which facilitates the O<sub>2</sub> activation and the desorption of *OH and enhances the catalytic activity of the Fe-N<sub>4</sub> site. Meanwhile, the unsaturated 5 d orbitals and tunable valence of the W atoms could modulate the electronic state of the Fe species, prevent leaching, and further enhance the catalytic stability. The resulting zinc-air battery with Fe,W-N-C air cathode exhibits notable cycling stability and repeatability for over 10,000 h. This enhanced stability highlights the possibility of developing 5 d metal-boosted 3 d metal active sites for the fabrication of efficient oxygen electrocatalysts and stable zinc-air batteries.