Size-effect induced controllable Cu<sup>0</sup>-Cu<sup>+</sup> sites for ampere-level nitrate electroreduction coupled with biomass upgrading.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 40064859.
- Also identified by DOI 10.1038/s41467-025-57097-x and PMC identifier 11893893.
- Licence recorded as CC BY-NC-ND.
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Abstract
The synergistic Cu<sup>0</sup>-Cu<sup>+</sup> sites is regarded as the active species towards NH<sub>3</sub> synthesis from the nitrate electrochemical reduction reaction (NO<sub>3</sub><sup>-</sup>RR) process. However, the mechanistic understanding and the roles of Cu<sup>0</sup> and Cu<sup>+</sup> remain exclusive. The big obstacle is that it is challenging to effectively regulate the interfacial motifs of Cu<sup>0</sup>-Cu<sup>+</sup> sites. In this paper, we describe the tunable construction of Cu<sup>0</sup>-Cu<sup>+</sup> interfacial structure by modulating the size-effect of Cu<sub>2</sub>O nanocube electrocatalysts to NO<sub>3</sub><sup>-</sup>RR performance. We elucidate the formation mechanism of Cu<sup>0</sup>-Cu<sup>+</sup> motifs by correlating the macroscopic particle size with the microscopic coordinated structure properties, and identify the synergistic effect of Cu<sup>0</sup>-Cu<sup>+</sup> motifs on NO<sub>3</sub><sup>-</sup>RR. Based on the rational design of Cu<sup>0</sup>-Cu<sup>+</sup> interfacial electrocatalyst, we develop an efficient paired-electrolysis system to simultaneously achieve the efficient production of NH<sub>3</sub> and 2,5-furandicarboxylic acid at an industrially relevant current densities (2 A cm<sup>-2</sup>), while maintaining high Faradaic efficiencies, high yield rates, and long-term operational stability in a 100 cm<sup>2</sup> electrolyzers, indicating promising practical applications.