The In Situ Assembly of an Equipotential Cathode for Nitrite Enrichment Enabling Electrochemical Nitrate Reduction to N<sub>2</sub>.
basic_science · Level V
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- Record sourced from PubMed, PMID 40227862.
- Also identified by DOI 10.1021/acs.nanolett.5c01401.
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Abstract
Electrocatalytically reducing NO<sub>3</sub><sup>-</sup> to N<sub>2</sub> is of great significance for environmental remediation and global nitrogen cycling. However, it is currently hindered by low N<sub>2</sub> selectivity since adsorbate N-intermediates are hard to migrate and couple each other during the N-N coupling step. Herein, an in situ assembly strategy was taken to attach Pd@Cu<sub>2</sub>O nanoparticles with CuO nanowire arrays to form an equipotential cathode CuO-Pd@Cu<sub>2</sub>O, which optimized N<sub>2</sub> selectivity to 91%, much higher than that of directly loaded Pd-Cu cathode (55%). Theoretical calculations combined with in situ spectroscopies demonstrated that the equipotential cathode can shield the electric field and enrich NO<sub>2</sub><sup>-</sup> intermediate inside. Meanwhile, a unique reaction pathway was revealed that the enriched NO<sub>2</sub><sup>-</sup> can directly couple with *N and also tune the Pd d-band center, avoiding the hurdles in N-N coupling. The approach here provides a new perspective in cathode design and a mechanistic understanding for the N-N coupling reaction.