Bilayer electrified-membrane with pair-atom tin catalysts for near-complete conversion of low concentration nitrate to dinitrogen.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 39875403.
- Also identified by DOI 10.1038/s41467-025-56102-7 and PMC identifier 11775098.
- Licence recorded as CC BY-NC-ND.
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Abstract
Discharge of wastewater containing nitrate (NO<sub>3</sub><sup>-</sup>) disrupts aquatic ecosystems even at low concentrations. However, selective and rapid reduction of NO<sub>3</sub><sup>-</sup> at low concentration to dinitrogen (N<sub>2</sub>) is technically challenging. Here, we present an electrified membrane (EM) loaded with Sn pair-atom catalysts for highly efficient NO<sub>3</sub><sup>-</sup> reduction to N<sub>2</sub> in a single-pass electrofiltration. The pair-atom design facilitates coupling of adsorbed N intermediates on adjacent Sn atoms to enhance N<sub>2</sub> selectivity, which is challenging with conventional fully-isolated single-atom catalyst design. The EM ensures sufficient exposure of the catalysts and intensifies the catalyst interaction with NO<sub>3</sub><sup>-</sup> through mass transfer enhancement to provide more N intermediates for N<sub>2</sub> coupling. We further develop a reduced titanium dioxide EM as the anode to generate free chlorines for fully oxidizing the residual ammonia (<1 mg-N L<sup>-1</sup>) to N<sub>2</sub>. The sequential cathode-to-anode electrofiltration realizes near-complete removal of 10 mg-N L<sup>-1</sup> NO<sub>3</sub><sup>-</sup> and ~100% N<sub>2</sub> selectivity with a water resident time on the order of seconds. Our findings advance the single-atom catalyst design for NO<sub>3</sub><sup>-</sup> reduction and provide a practical solution for NO<sub>3</sub><sup>-</sup> contamination at low concentrations.