Aligned d-orbital energy level of dual-atom sites catalysts for oxygen reduction reaction in anion exchange membrane fuel cells
Youze Zeng,
Xue Wang,
Wei Qi,
Changpeng Liu,
Lanlu Lu,
Meiling Xiao (),
Kai Li (),
Fei Xiao,
Minhua Shao (),
Wei Xing and
Jianbing Zhu ()
Additional contact information
Youze Zeng: Chinese Academy of Sciences
Xue Wang: Chinese Academy of Sciences
Wei Qi: Chinese Academy of Sciences
Changpeng Liu: Chinese Academy of Sciences
Lanlu Lu: Chinese Academy of Sciences
Meiling Xiao: Chinese Academy of Sciences
Kai Li: Chinese Academy of Sciences
Fei Xiao: Clear Water Bay
Minhua Shao: Clear Water Bay
Wei Xing: Chinese Academy of Sciences
Jianbing Zhu: Chinese Academy of Sciences
Nature Communications, 2025, vol. 16, issue 1, 1-13
Abstract:
Abstract The inherent scaling relationships between adsorption energies of oxygen-containing intermediates impose an intrinsic limitation on the maximum oxygen reduction reaction (ORR) activity, which represents one of the bottlenecks for the practical application of anion exchange membrane fuel cells (AEMFCs). To address this challenge, we align the 3dz2 orbital energy levels of Fe and Co to selectively customize the dissociative ORR pathway without the formation of OOH* intermediates, circumventing the conventional OH*-OOH* scaling relations. This rational design is achieved by atomic phosphorus(P) substitution, which not only optimizes orbital matching towards O-O cis-bridge adsorption, but also stabilizes the spontaneously adsorbed OH ligand as an electronic modifier. Due to these attributes, the well-designed FeCo-N/P-C catalyst demonstrates ORR performance with a current density of 251 mA·cm-2 at 0.9 ViR-free under 1.5 bar H2-O2, showing a competitive performance with state-of-the-art Pt-free electrocatalysts and meeting the 2025 DOE target (44 mA·cm-2). More importantly, the peak power density reaches as high as 0.805 W·cm-2 under 1.5 bar H2-air with negligible degradation observed over 10,000 cycles of voltage accelerated stress testing. This work offers a highly competitive electrocatalyst for AEMFCs and opens an effective avenue to bypass the constraints of linear scaling relations for ORR and beyond.
Date: 2025
References: Add references at CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/s41467-025-63322-4 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63322-4
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-025-63322-4
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().