Dinitrogen fixation by alkali and alkaline earth hydride composites under plasma

IF 2.7 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Kai Ma , Jianping Guo , Ping Chen
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Abstract

The development of alternative methods for sustainable dinitrogen (N2) fixation to ammonia (NH3) is a cutting-edge research area. The presence of external stimuli, such as non-thermal plasma, can boost the activation of the inert N2 molecules under ambient temperatures and pressures, thereby generating value-added products such as NH3 or other nitrogen-containing compounds. Binary alkali metal hydrides such as NaH and KH have recently shown intriguing properties in the plasma nitrogen fixation process. Herein we report the different chemical behaviors of a series of hydride composites consist of potassium hydride (KH) and alkaline earth metal hydride (MgH2, CaH2, SrH2, and BaH2) under nitrogen plasma conditions. A nitrogen-relayed mechanism has been proposed to understand the different nitrogen fixation behaviors on these hydride composites. Under this scenario, KH is responsible for plasma N2 fixation to form surface NH2 species, which subsequently migrate and react with MgH2, CaH2, and SrH2 to form N and NH species, respectively. This work enriches the plasma chemistry of metal hydrides, and provides a strategy to enhance the amounts of fixed nitrogen of single hydride material under nitrogen plasma conditions.

Abstract Image

等离子体下碱与碱土氢化物复合材料固氮
开发可持续的二氮(N2)固定到氨(NH3)的替代方法是一个前沿研究领域。外部刺激的存在,如非热等离子体,可以促进惰性N2分子在环境温度和压力下的活化,从而产生增值产品,如NH3或其他含氮化合物。二元碱金属氢化物如NaH和KH最近在等离子体固氮过程中显示出有趣的特性。本文报道了由氢化钾(KH)和碱土金属氢化物(MgH2、CaH2、SrH2和BaH2)组成的一系列氢化物复合材料在氮等离子体条件下的不同化学行为。我们提出了一种氮传递机制来理解这些氢化物复合材料不同的固氮行为。在这种情况下,KH负责血浆N2固定形成表面NH2, NH2随后迁移并与MgH2, CaH2和SrH2分别反应形成N和NH。本工作丰富了金属氢化物的等离子体化学,为提高氮等离子体条件下单个氢化物材料的固定氮量提供了一种策略。
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来源期刊
Inorganica Chimica Acta
Inorganica Chimica Acta 化学-无机化学与核化学
CiteScore
6.00
自引率
3.60%
发文量
440
审稿时长
35 days
期刊介绍: Inorganica Chimica Acta is an established international forum for all aspects of advanced Inorganic Chemistry. Original papers of high scientific level and interest are published in the form of Articles and Reviews. Topics covered include: • chemistry of the main group elements and the d- and f-block metals, including the synthesis, characterization and reactivity of coordination, organometallic, biomimetic, supramolecular coordination compounds, including associated computational studies; • synthesis, physico-chemical properties, applications of molecule-based nano-scaled clusters and nanomaterials designed using the principles of coordination chemistry, as well as coordination polymers (CPs), metal-organic frameworks (MOFs), metal-organic polyhedra (MPOs); • reaction mechanisms and physico-chemical investigations computational studies of metalloenzymes and their models; • applications of inorganic compounds, metallodrugs and molecule-based materials. Papers composed primarily of structural reports will typically not be considered for publication.
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