Sustainable conversion of alkaline nitrate to ammonia at activities greater than 2 A cm<sup>-2</sup>.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 38341446.
- Also identified by DOI 10.1038/s41467-024-45534-2 and PMC identifier 10858923.
- 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
Nitrate (NO<sub>3</sub><sup>‒</sup>) pollution poses significant threats to water quality and global nitrogen cycles. Alkaline electrocatalytic NO<sub>3</sub><sup>‒</sup> reduction reaction (NO<sub>3</sub>RR) emerges as an attractive route for enabling NO<sub>3</sub><sup>‒</sup> removal and sustainable ammonia (NH<sub>3</sub>) synthesis. However, it suffers from insufficient proton (H<sup>+</sup>) supply in high pH conditions, restricting NO<sub>3</sub><sup>‒</sup>-to-NH<sub>3</sub> activity. Herein, we propose a halogen-mediated H<sup>+</sup> feeding strategy to enhance the alkaline NO<sub>3</sub>RR performance. Our platform achieves near-100% NH<sub>3</sub> Faradaic efficiency (pH = 14) with a current density of 2 A cm<sup>-2</sup> and enables an over 99% NO<sub>3</sub><sup>-</sup>-to-NH<sub>3</sub> conversion efficiency. We also convert NO<sub>3</sub><sup>‒</sup> to high-purity NH<sub>4</sub>Cl with near-unity efficiency, suggesting a practical approach to valorizing pollutants into valuable ammonia products. Theoretical simulations and in situ experiments reveal that Cl-coordination endows a shifted d-band center of Pd atoms to construct local H<sup>+</sup>-abundant environments, through arousing dangling O-H water dissociation and fast *H desorption, for *NO intermediate hydrogenation and finally effective NO<sub>3</sub><sup>‒</sup>-to-NH<sub>3</sub> conversion.