Iron atom-cluster interactions increase activity and improve durability in Fe-N-C fuel cells.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 35618792.
- Also identified by DOI 10.1038/s41467-022-30702-z and PMC identifier 9135695.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Simultaneously increasing the activity and stability of the single-atom active sites of M-N-C catalysts is critical but remains a great challenge. Here, we report an Fe-N-C catalyst with nitrogen-coordinated iron clusters and closely surrounding Fe-N<sub>4</sub> active sites for oxygen reduction reaction in acidic fuel cells. A strong electronic interaction is built between iron clusters and satellite Fe-N<sub>4</sub> due to unblocked electron transfer pathways and very short interacting distances. The iron clusters optimize the adsorption strength of oxygen reduction intermediates on Fe-N<sub>4</sub> and also shorten the bond amplitude of Fe-N<sub>4</sub> with incoherent vibrations. As a result, both the activity and stability of Fe-N<sub>4</sub> sites are increased by about 60% in terms of turnover frequency and demetalation resistance. This work shows the great potential of strong electronic interactions between multiphase metal species for improvements of single-atom catalysts.