Full runner electrolyzer stack for industrial-current-density NOx−-mediated ammonia synthesis from air and water

作者：Wei Liu, Yang Lv, Honghui Ou, Jiayi Zhang, Yumei Ren, Mengyang Xia, Yang Li, He Li, Xiaoling Ren, Huagui Hu, Guidong Yang · 发表于：Nature Communications · 年份：2025 · DOI：10.1038/s41467-025-61069-6 · 被引用次数：34 · 研究领域：Ammonia Synthesis and Nitrogen Reduction、Caching and Content Delivery、Catalytic Processes in Materials Science

Plasma-electrochemical tandem conversion with NOx− as intermediates promises a route for renewable ammonia (NH3) synthesis from air and water. However, a critical challenge lies in developing electrolyzers capable of operating efficiently at large current densities. Here, we present a scalable membrane electrode assembly electrolyzer with a full runner design (MEA-FR) that achieves efficient NH3 production at industrial current densities. Compared to conventional serpentine runner configuration, MEA-FR leveraging forced convection within porous electrodes achieves three-order-of-magnitude enhancement in NOx− mass transfer flux. This design, meanwhile, generates strong shear forces across the porous electrode, promoting rapid detachment of O2 bubbles at the anode and reducing overpotential losses. Notably, MEA-FR exhibits a high Faradaic efficiency of 91.8 ± 1.4% for NH3 synthesis at 500 mA cm−2, significantly outperforming the serpentine runner counterparts (64.9 ± 1.1%). Furthermore, a scaled-up 4 × 25 cm2 MEA-FR stack with four modular cells is assembled with rotationally symmetric bipolar plates, delivering high NOx− conversion efficiency (>95%), high Faradaic efficiency (>91%), and long-term stability (>200 h) under industrial-relevant current densities. Electrolyzers operating efficiently at industrial current densities offer promise but face challenges for practical NOx− -to-ammonia conversion. Here, the authors report a full runner electrolyzer stack that enhances mass...