Ampere-Level Nitrate Electroreduction to Ammonia over Monodispersed Bi-Doped FeS<sub>2</sub>.
basic_science · Level V
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- Record sourced from PubMed, PMID 37870919.
- Also identified by DOI 10.1021/acsnano.3c05946.
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Abstract
Electrochemical conversion of NO<sub>3</sub><sup>-</sup> into NH<sub>3</sub> (NO<sub>3</sub>RR) holds an enormous prospect to simultaneously yield valuable NH<sub>3</sub> and alleviate NO<sub>3</sub><sup>-</sup> pollution. Herein, we report monodispersed Bi-doped FeS<sub>2</sub> (Bi-FeS<sub>2</sub>) as a highly effective NO<sub>3</sub>RR catalyst. Atomic coordination characterizations of Bi-FeS<sub>2</sub> disclose that the isolated Bi dopant coordinates with its adjacent Fe atom to create the unconventional p-d hybridized Bi-Fe dinuclear sites. Operando spectroscopic measurements combined with theoretical calculations disclose that Bi-Fe dinuclear sites can synergistically enhance the hydrogenation energetics of NO<sub>3</sub><sup>-</sup>-to-NH<sub>3</sub> pathway, while suppressing the competitive hydrogen evolution, leading to a high NO<sub>3</sub>RR selectivity and activity. Consequently, the specially designed flow cell equipped with Bi-FeS<sub>2</sub> exhibits a high NH<sub>3</sub> yield rate of 83.7 mg h<sup>-1</sup> cm<sup>-2</sup> with a near-100% NO<sub>3</sub><sup>-</sup>-to-NH<sub>3</sub> Faradaic efficiency at an ampere-level current density of 1023.2 mA cm<sup>-2</sup>, together with an excellent long-term stability for 100 h of electrolysis, ranking almost the highest performance among all reported NO<sub>3</sub>RR catalysts.