Abstract

Polymeric nitrogen, stabilized by compressing pure molecular nitrogen, has yet to be recovered to ambient conditions, precluding its application as a high-energy density material. Here we suggest a route for synthesis of a tetragonal polymeric nitrogen, denoted t-N, via He-N compounds at high pressures. Using first-principles calculations with structure searching, we predict a class of nitrides with stoichiometry HeN4 that are energetically stable (relative to a mixture of solid He and N2) above 8.5 GPa. At high pressure, HeN4 comprises a polymeric channel-like nitrogen framework filled with linearly arranged helium atoms. The nitrogen framework persists to ambient pressure on decompression after removal of helium, forming pure polymeric nitrogen, t-N. t-N is dynamically and mechanically stable at ambient pressure with an estimated energy density of ~11.31 kJ/g, marking it out as a remarkable high-energy density material. This expands the known polymeric forms of nitrogen and indicates a route to its synthesis.

Details

Title
Route to high-energy density polymeric nitrogen t-N via He−N compounds
Author
Li, Yinwei 1 ; Feng, Xiaolei 2 ; Liu, Hanyu 3 ; Hao, Jian 1 ; Redfern, Simon A T 4   VIAFID ORCID Logo  ; Lei, Weiwei 5 ; Liu, Dan 5 ; Ma, Yanming 6 

 School of Physics and Electronic Engineering, Jiangsu Normal University, Xuzhou, China 
 State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun, China; Department of Earth Sciences, University of Cambridge, Cambridge, UK 
 Geophysical Laboratory, Carnegie Institution of Washington, Washington, DC, USA 
 Department of Earth Sciences, University of Cambridge, Cambridge, UK; Center for High Pressure Science and Technology Advanced Research (HPSTAR), Shanghai, China 
 Institute for Frontier Materials, Deakin University, Waurn Ponds, VIC, Australia 
 State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun, China; International Center of Future Science, Jilin University, Changchun, China 
Pages
1-7
Publication year
2018
Publication date
Feb 2018
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2004118089
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.