Improving Plasma-Catalytic Ammonia Synthesis Using a Coaxial Double-Helix-Electrode Reactor

利用同轴双螺旋电极反应器改进等离子体催化氨合成

阅读:3

Abstract

Developing energy-efficient ammonia synthesis under mild and carbon-neutral conditions remains a major challenge for sustainable nitrogen fixation. Here, we present a coaxial double-helix-electrode-based double-dielectric barrier discharge (DBD) reactor, termed a "double-helix" design, featuring dual quartz barriers and symmetric high-voltage and grounded electrodes to achieve uniform, high-intensity volume discharge for plasma-catalytic ammonia synthesis. Three-dimensional electrostatic simulations demonstrate that this configuration generates a strongly coupled and spatially homogeneous electric field (∼7 × 10(6) V m(-1)), significantly outperforming conventional single-dielectric DBD designs (∼1 × 10(6) V m(-1)). An optimized Ni electrode with a 1 mm winding pitch increases electron density, as evidenced by optical emission spectroscopy (OES, I(N2+)(425 nm)/I(N2*)(335 nm) = 0.15). Under plasma-only operation, the double-helix DBD reactor produces approximately 2.5-fold higher NH(3) concentration than a conventional DBD at identical power input. When integrated with a Ni/Al(2)O(3) catalyst, synergistic plasma-catalyst interactions further enhance ammonia yield and energy efficiency, achieving an energy yield of up to 3.68 g NH(3) kWh(-1) under 5.92 W discharge. Comprehensive analysis combining electric-field simulations, transient discharge imaging, and catalytic performance measurements elucidates the intrinsic coupling between electrode architecture, discharge physics, and catalytic function. This work demonstrates that electric-field engineering is an effective strategy for enabling stable volume discharge and enhancing plasma-catalytic ammonia synthesis, offering a generic design principle for next-generation low-carbon nitrogen-fixation systems.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。