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碱金属和碱土金属氢化物驱动的氮在氮化锰催化剂上的活化与转化

Alkali and Alkaline Earth Hydrides-Driven N Activation and Transformation over Mn Nitride Catalyst.

作者信息

Chang Fei, Guan Yeqin, Chang Xinghua, Guo Jianping, Wang Peikun, Gao Wenbo, Wu Guotao, Zheng Jie, Li Xingguo, Chen Ping

机构信息

Dalian National Laboratory for Clean Energy , Dalian Institute of Chemical Physics, Chinese Academy of Sciences , Dalian 116023 , P. R. China.

University of Chinese Academy of Sciences , Beijing 100049 , P. R. China.

出版信息

J Am Chem Soc. 2018 Nov 7;140(44):14799-14806. doi: 10.1021/jacs.8b08334. Epub 2018 Oct 23.

DOI:10.1021/jacs.8b08334
PMID:30351925
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, CaH and BaH, AHs for short) promotes the catalytic activity of Mn nitride by orders of magnitude. The sequence of promotion is BaH > LiH > KH > CaH > 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 N activation and subsequent conversion to NH. 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.

摘要

早期的3d过渡金属并非许多化学过程的重点催化候选物,因为它们对O、N、C或H等具有很强的亲和力,这会阻碍这些物种转化为产物。以金属锰为例,在氨合成条件下会发生氮化反应形成体相氮化物,遗憾的是其催化活性可忽略不计。在此我们表明,碱金属或碱土金属氢化物(即LiH、NaH、KH、CaH和BaH,简称为AHs)能将氮化锰的催化活性提高几个数量级。促进作用的顺序为BaH > LiH > KH > CaH > NaH,这与传统氧化物或氢氧化物促进剂中观察到的顺序不同。AHs的特征是带有带负电荷的氢原子,具有从氮化锰中去除N的化学势,从而导致N活化显著增强并随后转化为NH。对Mn-LiH催化体系的详细研究表明,活性相和动力学行为强烈依赖于反应条件。基于对AHs与氮化锰之间协同作用的理解,提出了一种设计和开发早期过渡金属作为氨合成及其他化学过程有效催化剂的策略。

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