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Fe-N system at high pressure reveals a compound featuring polymeric nitrogen chains.

Authors :
Bykov M
Bykova E
Aprilis G
Glazyrin K
Koemets E
Chuvashova I
Kupenko I
McCammon C
Mezouar M
Prakapenka V
Liermann HP
Tasnádi F
Ponomareva AV
Abrikosov IA
Dubrovinskaia N
Dubrovinsky L
Source :
Nature communications [Nat Commun] 2018 Jul 16; Vol. 9 (1), pp. 2756. Date of Electronic Publication: 2018 Jul 16.
Publication Year :
2018

Abstract

Poly-nitrogen compounds have been considered as potential high energy density materials for a long time due to the large number of energetic N-N or N=N bonds. In most cases high nitrogen content and stability at ambient conditions are mutually exclusive, thereby making the synthesis of such materials challenging. One way to stabilize such compounds is the application of high pressure. Here, through a direct reaction between Fe and N <subscript>2</subscript> in a laser-heated diamond anvil cell, we synthesize three ironnitrogen compounds Fe <subscript>3</subscript> N <subscript>2</subscript> , FeN <subscript>2</subscript> and FeN <subscript>4</subscript> . Their crystal structures are revealed by single-crystal synchrotron X-ray diffraction. Fe <subscript>3</subscript> N <subscript>2</subscript> , synthesized at 50 GPa, is isostructural to chromium carbide Cr <subscript>3</subscript> C <subscript>2</subscript> . FeN <subscript>2</subscript> has a marcasite structure type and features covalently bonded dinitrogen units in its crystal structure. FeN <subscript>4</subscript> , synthesized at 106 GPa, features polymeric nitrogen chains of [N <subscript>4</subscript> <superscript>2-</superscript> ] <subscript>n</subscript> units. Based on results of structural studies and theoretical analysis, [N <subscript>4</subscript> <superscript>2-</superscript> ] <subscript>n</subscript> units in this compound reveal catena-poly[tetraz-1-ene-1,4-diyl] anions.

Details

Language :
English
ISSN :
2041-1723
Volume :
9
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
30013071
Full Text :
https://doi.org/10.1038/s41467-018-05143-2