Li Ji, Wu Kai, Heng Jing, Zhu Lintao, Wang Xuechuan, Han Qingxin, Qiang Taotao
College of Bioresources and Materials Engineering, Shaanxi University of Science & Technology, Xi'an, 710 021, P. R. China.
College of Chemistry, Nankai University, Weijin Road No. 94, Tianjin, 300 071, China.
Small. 2025 Mar;21(9):e2411005. doi: 10.1002/smll.202411005. Epub 2025 Jan 29.
The electrochemical reduction of nitrate to ammonia offers an environmentally sustainable pathway for nitrogen fixation. However, achieving both efficiency and selectivity in nitrate reduction presents a formidable challenge, due to the involvement of sluggish multielectron transfer processes. Herein, the successful synthesis of spherical Cu₂O nanoparticles (s-Cu₂O) exhibiting significant compressive strain effects, achieved through a one-pot method using gelatin as a structural modifier, is reported. The s-Cu₂O catalyst demonstrates exceptional electrochemical performance for nitrate reduction reaction (NORR), achieving a Faradaic efficiency (FE) of 95.07%, ammonia selectivity of 92.03%, a nitrate conversion rate of 97.77%, and a yield rate of 284.83 µmol h⁻¹ cm⁻ at -0.8 V versus reversible hydrogen electrode (vs. RHE) for ammonia production. Structural characterization and density functional theory calculations reveal that compressive strain plays a critical role in modulating the electronic structure of the catalyst, thereby activating the *NO intermediate in the potential determining step and effectively suppressing the hydrogen evolution reaction. Furthermore, it is implemented in a Zn-NO battery, and the test results indicate that the battery achieved a peak power density of 3.95 mW cm at a potential of 0.129 V (vs Zn/Zn⁺), illustrating its excellent electrochemical and functional efficacy. This work introduces a novel strategy for the rational design of high-performance electrocatalysts through strain engineering, offering broad implications for energy-efficient ammonia synthesis, and sustainable nitrogen cycling.