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Fe(II)-rich catalytic interfaces boost nitrate adsorption and hydrogenation for selective electrochemical ammonia synthesis
DOI:10.1016/j.cej.2025.166686.png)
Abstract
En 中文
• Fe@CF-1 achieves 98.46% NO3− conversion within 2 h across a wide pH range (3–12). • Stabilized Fe(II) sites have the ability to effectively adsorb and activate NO3−. • Fe sites promote hydrogenation of nitrogenous intermediates while inhibiting HER. • Fe@CF-1 shows dynamic evolution of Fe(II) and Fe(III) species during NO3RR.
Keywords:
Fe@CF-1
NO3− reduction
Fe(II) sites
hydrogenation
HER inhibition
Journal
IF:
13.2
Papers:
7.4W
Citations:
48.5W

