| Literature DB >> 30351925 |
Fei Chang1,2, Yeqin Guan1,2, Xinghua Chang3, Jianping Guo1,4, Peikun Wang1,2, Wenbo Gao1,2, Guotao Wu1, Jie Zheng3, Xingguo Li3, Ping Chen1,4.
Abstract
Early 3d transition metals are not focal catalytic candidates for many chemical processes because they have strong affinities to O, N, C, or H, etc., which would hinder the conversion of those species to products. Metallic Mn, as a representative, undergoes nitridation under ammonia synthesis conditions forming bulk phase nitride and unfortunately exhibits negligible catalytic activity. Here we show that alkali or alkaline earth metal hydrides (i.e., LiH, NaH, KH, CaH2 and BaH2, AHs for short) promotes the catalytic activity of Mn nitride by orders of magnitude. The sequence of promotion is BaH2 > LiH > KH > CaH2 > NaH, which is different from the order observed in conventional oxide or hydroxide promoters. AHs, featured by bearing negatively charged hydrogen atoms, have chemical potentials in removing N from Mn nitride and thus lead to significant enhancement of N2 activation and subsequent conversion to NH3. Detailed investigations on Mn-LiH catalytic system disclosed that the active phase and kinetic behavior depend strongly on reaction conditions. Based on the understanding of the synergy between AHs and Mn nitride, a strategy in the design and development of early transition metals as effective catalysts for ammonia synthesis and other chemical processes is proposed.Entities:
Year: 2018 PMID: 30351925 DOI: 10.1021/jacs.8b08334
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419