On the mechanism for the plasma-activated N2 dissociation on Ru surfaces

被引:18
|
作者
Rouwenhorst, Kevin H. R. [1 ]
Lefferts, Leon [1 ]
机构
[1] Univ Twente, MESA Inst Nanotechnol, Catalyt Proc & Mat, POB 217, NL-7500 AE Enschede, Netherlands
关键词
ammonia; plasma catalysis; ruthenium; N-2; dissociation; CATALYTIC AMMONIA-SYNTHESIS; NONTHERMAL PLASMA; MOLECULAR-BEAM; SCALING RELATIONS; ADSORPTION; RUTHENIUM; RU(0001); METHANE; ENERGY; CHEMISORPTION;
D O I
10.1088/1361-6463/ac1226
中图分类号
O59 [应用物理学];
学科分类号
摘要
Plasma-activation of N-2 via vibrational excitations or electronic excitations enhances the dissociative sticking probability on Ru-surfaces with respect to ground-state N-2. We propose that this is primarily due to a weaker nitrogen-nitrogen bond, facilitating direct adsorption of both nitrogen atoms on the metallic surface, a pathway with a high barrier for ground-state N-2 due to the short bond distance of 110 pm. Furthermore, we show that the increased sticking probability is not only a heating artefact, as the activation barrier for N-2 dissociation decreases upon plasma-activation. Recent modelling studies show that the binding strengths of surface adsorbates, as well as the barrier for dissociation may change as a result of high electric fields, as well as high degrees of charging metal particles. We show that the effect of plasma-induced electric fields is negligible in dielectric barrier discharge reactors, and other non-thermal plasma reactors. The effect of alkali promoters on the local electric fields is orders of magnitude larger than the electric field of the plasma. The role of plasma-induced metal surface charging during N-2 dissociation is currently not known for metal clusters on a support.
引用
收藏
页数:10
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