Silva Tiago, Bera Susanta, Pintassilgo Carlos D, Herrmann Anja, Welzel Stefan, Tsampas Mihalis N, van de Sanden Mauritius C M, Alves Luís L, Guerra Vasco
Instituto de Plasmas e Fusão Nuclear (IPFN), Instituto Superior Técnico, Universidade de Lisboa, 1049-001 Lisboa, Portugal.
Dutch Institute for Fundamental Energy Research (DIFFER), 5612 AJ Eindhoven, the Netherlands.
J Phys Chem A. 2024 Aug 29;128(34):7235-7256. doi: 10.1021/acs.jpca.4c03323. Epub 2024 Aug 19.
This work presents a detailed investigation aimed at understanding the key mechanisms governing nitric oxide (NO) production in N-O discharges by systematically comparing experimental results to modeling data. The experimental phase capitalizes on radiofrequency (13.56 MHz) discharges, sustained at 5 mbar pressure conditions, featuring varying concentrations of oxygen, ranging from pure N plasma to air-like mixtures. On the modeling front, we adopt an integrated approach that combines the solution of the Boltzmann equation for electrons with a system of rate balance equations for heavy species. To account for ground state NO(X) generation at the reactor wall, we combine the volume chemistry with a mesoscopic description of the surface, taking into account adsorption sites and various elementary surface phenomena. Comparisons between experiments and modeling demonstrate very good agreement, extending beyond NO(X) formation to encompass other species in the plasma such as NO(X) and atomic nitrogen N(S). Noteworthy findings include (i) the pivotal role of surface mechanisms in NO(X) production, particularly at low oxygen content values; (ii) the significance of accurately describing the postdischarge phase, where depletion of plasma species occurs at different time scales (millisecond range); and (iii) the importance of vibrationally and electronically excited states (e.g., O(b)) in elucidating NO(X) formation dynamics, crucial for unraveling reaction pathways and energy transfer processes. This work makes an important step toward formulating a comprehensive reaction mechanism for N and N-O plasmas applied to nitrogen fixation, covering both volume and surface mechanisms, and lays a robust foundation for future research on plasma-based NO(X) production, particularly in the presence of catalysts.
这项工作进行了详细的研究,旨在通过系统地将实验结果与建模数据进行比较,来理解氮氧放电中一氧化氮(NO)生成的关键机制。实验阶段利用了射频(13.56 MHz)放电,在5毫巴的压力条件下维持,其氧气浓度不同,范围从纯氮等离子体到类似空气的混合物。在建模方面,我们采用了一种综合方法,将电子的玻尔兹曼方程的解与重粒子的速率平衡方程组相结合。为了考虑反应堆壁上基态NO(X)的生成,我们将体积化学与表面的介观描述相结合,同时考虑吸附位点和各种基本表面现象。实验与建模之间的比较表明,两者吻合得非常好,不仅涵盖了NO(X)的形成,还包括等离子体中的其他物种,如NO(X)和原子氮N(S)。值得注意的发现包括:(i)表面机制在NO(X)生成中起关键作用,特别是在低氧含量值时;(ii)准确描述放电后阶段的重要性,在该阶段等离子体物种在不同时间尺度(毫秒范围)内发生消耗;(iii)振动和电子激发态(如O(b))在阐明NO(X)形成动力学中的重要性,这对于揭示反应途径和能量转移过程至关重要。这项工作朝着为应用于固氮的氮和氮氧等离子体制定全面的反应机制迈出了重要一步,涵盖了体积和表面机制,为未来基于等离子体的NO(X)生成研究,特别是在有催化剂存在的情况下,奠定了坚实的基础。