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用于从空气和水中以工业电流密度进行NO介导氨合成的全尺寸流动电解槽堆栈。

Full runner electrolyzer stack for industrial-current-density NO-mediated ammonia synthesis from air and water.

作者信息

Liu Wei, Lv Yang, Ou Honghui, Zhang Jiqiu, Ren Yuxi, Xia Mengyang, Li Yang, Li He, Ren Xiaoling, Hu Huagui, Yang Guidong

机构信息

State Key Laboratory of Fluorine & Nitrogen Chemicals, School of Chemical Engineering and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi, China.

China Energy Yulin Chemical Company, Yulin, P.R. China.

出版信息

Nat Commun. 2025 Jul 1;16(1):5716. doi: 10.1038/s41467-025-61069-6.

Abstract

Plasma-electrochemical tandem conversion with NO as intermediates promises a route for renewable ammonia (NH) 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 NH 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 NO mass transfer flux. This design, meanwhile, generates strong shear forces across the porous electrode, promoting rapid detachment of O bubbles at the anode and reducing overpotential losses. Notably, MEA-FR exhibits a high Faradaic efficiency of 91.8 ± 1.4% for NH synthesis at 500 mA cm, significantly outperforming the serpentine runner counterparts (64.9 ± 1.1%). Furthermore, a scaled-up 4 × 25 cm MEA-FR stack with four modular cells is assembled with rotationally symmetric bipolar plates, delivering high NO conversion efficiency (>95%), high Faradaic efficiency (>91%), and long-term stability (>200 h) under industrial-relevant current densities.

摘要

以一氧化氮(NO)作为中间体的等离子体电化学串联转化为从空气和水中合成可再生氨(NH₃)提供了一条途径。然而,一个关键挑战在于开发能够在大电流密度下高效运行的电解槽。在此,我们展示了一种具有全流道设计的可扩展膜电极组件电解槽(MEA-FR),它能在工业电流密度下实现高效的氨生产。与传统的蛇形流道配置相比,MEA-FR利用多孔电极内的强制对流使NO传质通量提高了三个数量级。同时,这种设计在多孔电极上产生强大的剪切力,促进阳极处氧气泡的快速脱离并减少过电位损失。值得注意的是,MEA-FR在500 mA cm²下氨合成的法拉第效率高达91.8±1.4%,显著优于蛇形流道的同类产品(64.9±1.1%)。此外,一个由四个模块化电池组成的4×25 cm²的MEA-FR放大堆栈与旋转对称双极板组装在一起,在与工业相关的电流密度下实现了高NO转化效率(>95%)、高法拉第效率(>91%)和长期稳定性(>200小时)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78b0/12216532/34510b98fc27/41467_2025_61069_Fig1_HTML.jpg

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