Abstract

The electrochemical nitrogen reduction reaction (NRR) offers a sustainable pathway for ammonia synthesis under ambient conditions. Among these, vacancy engineering has emerged as an effective approach to accelerate nitrogen-to-ammonia conversion and enhance electrocatalytic performance. However, the controllable synthesis of catalysts with precise cation vacancy concentrations remains a significant challenge. In this study, we address this by employing a combined thermal treatment and plasma approach to fabricate copper selenide nanosheets with precisely tuned copper vacancy (V<sub>Cu</sub>) concentrations. The resulting p-Cu<sub>1.8</sub>Se/Cu<sub>2</sub>Se/C-5 catalyst, possessing the highest V<sub>Cu</sub> concentration, demonstrated superior NRR activity, achieving an NH<sub>3</sub> production rate of 21.81 μg h<sup>-1</sup> mg<sub>cat.</sub><sup>-1</sup> at -0.7 V vs the reversible hydrogen electrode (RHE), a value more than 3-fold higher than that of its vacancy-free counterpart. These results indicate that V<sub>Cu</sub> sites serve as active centers that optimize nitrogen adsorption and activation, thereby significantly lowering the energy barrier of the rate-determining step. This work provides a new avenue for designing next-generation, high-performance NRR electrocatalysts through precise defect engineering.

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Year
2025
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Xiaohan Li, Shuo Chen, Yuao Wei et al. (2025). Copper Selenide Nanosheet with Adjustable Cation Vacancy for Boosting Nitrogen Electroreduction. ACS Applied Materials & Interfaces . https://doi.org/10.1021/acsami.5c20585

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DOI
10.1021/acsami.5c20585