Sustainable conversion of alkaline nitrate to ammonia at activities greater than 2 A cm<sup>-2</sup>.

Liao, Wanru; Wang, Jun; Ni, Ganghai; Liu, Kang; Liu, Changxu; Chen, Shanyong; Wang, Qiyou; Chen, Yingkang et al. · Nat Commun · 2024

basic_science · Level V

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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.