Plasma‐Driven Nitrogen Fixation on Sodium Hydride

Author:

Wu Han12,Yang Liang13,Wen Jiaqi12,Xu Yongfeng13,Cai Yongli12,Gao Wenbo12,Wang Qianru12,Guan Yeqin12,Feng Sheng12,Cao Hujun12,He Teng12,Liu Lin12,Zhang Shaoqian13,Guo Jianping12ORCID,Chen Ping12ORCID

Affiliation:

1. Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

2. Center of Materials and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing 100049 China

3. Key Laboratory of Chemical Lasers Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

Abstract

AbstractThe development of alternative approaches to the conventional Haber–Bosch ammonia synthesis process is an imperative but very challenging task. Extrinsic stimuli such as plasma could provide greater flexibility in materials selection and process innovation for nitrogen fixation. Hydride (hydrogen anion, H‾)‐containing materials have recently shown promise in thermal ammonia synthesis, whereas the interactions of hydrides and N2 under plasma have rarely been investigated. Herein we explore plasma‐driven nitrogen fixation to NH3 mediated by an inexpensive and common reagent sodium hydride, which does not react with N2 under normal thermal conditions. Nitrogen plasma can produce reactive nitrogen species and also induce the dehydriding of NaH, which result in the activation and hydrogenation of N2 to surface NaNH2 species. The subsequent thermal‐hydrogenation of NaNH2 produces NH3 facilely. The stepwise chemical loop prevents ammonia from plasma‐induced cracking. This NaH‐mediated chemistry broadens the scope of hydrides as well as many other materials for N2 fixation, and also has prospect for other chemical transformations.

Funder

National Natural Science Foundation of China

Youth Innovation Promotion Association of the Chinese Academy of Sciences

Liaoning Revitalization Talents Program

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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