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Current ammonia (NH₃) synthesis is hindered by challenges including N₂ activation, NH₃ separation and process complexity. Here, we report a plasma‐electrochemical process for the production of gaseous ammonia from air generated NO x , decoupled from processes employing liquid phase intermediaries such as NO₃⁻ and final product (NH 4 + ). Importantly, this process uses air for scalable ammonia production under ambient conditions and directly produces gaseous NH₃ which facilitates efficient product separation. For NO x reduction to NH₃, we propose a universal strategy combining plasma pretreatment and wet chemical calcination to introduce multifunctional oxygen vacancies. The resulting highly defective Fe₂O₃ nanoparticles on Cu achieves a significant ammonia production rate of 628 nmol·s⁻¹·cm⁻ 2 , along with nearly 100% faradaic efficiency.
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Xu et al. (2025) studied this question.
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