Ferromagnetic Fe-TiO<sub>2</sub> spin catalysts for enhanced ammonia electrosynthesis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39875424.
- Also identified by DOI 10.1038/s41467-025-56566-7 and PMC identifier 11775347.
- 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
Magnetic field effects (MFE) of ferromagnetic spin electrocatalysts have attracted significant attention due to their potential to enhance catalytic activity under an external magnetic field. However, no ferromagnetic spin catalysts have demonstrated MFE in the electrocatalytic reduction of nitrate for ammonia (NO<sub>3</sub>RR), a pioneering approach towards NH<sub>3</sub> production involving the conversion from diamagnetic NO<sup>3</sup><sup>-</sup> to paramagnetic NO. Here, we report the ferromagnetic Fe-TiO<sub>2</sub> to investigate MFE on NO<sub>3</sub>RR. Fe-TiO<sub>2</sub> possesses a high density of atomically dispersed Fe sites and exhibits an intermediate-spin state, resulting in magnetic ordering through ferromagnetism. Assisted by a magnetic field, Fe-TiO<sub>2</sub> achieves a Faradaic efficiency (FE) of up to 97% and an NH<sub>3</sub> yield of 24.69 mg mg<sub>cat</sub><sup>-</sup><sup>1</sup> at -0.5 V versus reversible hydrogen electrode. Compared to conditions without an external magnetic field, the FE and NH<sub>3</sub> yield for Fe-TiO<sub>2</sub> under an external magnetic field is increased by ~21.8% and ~ 3.1 times, respectively. In-situ characterization and theoretical calculations show that spin polarization enhances the critical step of NO hydrogenation to NOH by optimizing electron transfer pathways between Fe and NO, significantly boosting NO<sub>3</sub>RR activity.