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X-ray Free Electron Laser-Induced Synthesis of ε-Iron Nitride at High Pressures
Author(s) -
Huijeong Hwang,
Taehyun Kim,
Hyunchae Cynn,
Thomas Vogt,
Rachel Husband,
Karen Appel,
Carsten Baehtz,
Orianna B. Ball,
M. Baron,
R.J. Briggs,
Maxim Bykov,
Elena Bykova,
Valerio Cerantola,
Julien Chantel,
A. L. Coleman,
Dana Dattlebaum,
Leora E. DresselhausMarais,
J. H. Eggert,
Lars Ehm,
W.J. Evans,
G. Fiquet,
Mungo Frost,
Konstantin Glazyrin,
Alexander F. Goncharov,
Zsolt Jenei,
Jaeyong Kim,
Zuzana Konôpková,
Jona Mainberger,
Mikako Makita,
Hauke Marquardt,
E. E. McBride,
J. McHardy,
Sébastien Merkel,
G. Morard,
Earl F. O’Ban,
Christoph Otzen,
Edward J. Pace,
A. Pełka,
Charles Pépin,
J. S. Pigott,
Vitali B. Prakapenka,
Clemens Prescher,
R. Redmer,
S. Speziale,
Georg Spiekermann,
C. Strohm,
Blake T. Sturtevant,
Nenad Velisavljevic,
Max Wilke,
Choong-Shik Yoo,
U. Zastrau,
HannsPeter Liermann,
M. I. McMahon,
R. S. McWilliams,
Yongjae Lee
Publication year - 2021
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.1c00150
Subject(s) - free electron laser , diamond anvil cell , ultrashort pulse , laser , x ray , irradiation , cathode ray , materials science , electron , nitride , diamond , atomic physics , high pressure , analytical chemistry (journal) , pulse (music) , chemistry , optics , physics , thermodynamics , nanotechnology , metallurgy , layer (electronics) , quantum mechanics , chromatography , detector , nuclear physics
The ultrafast synthesis of ε-Fe 3 N 1+ x in a diamond-anvil cell (DAC) from Fe and N 2 under pressure was observed using serial exposures of an X-ray free electron laser (XFEL). When the sample at 5 GPa was irradiated by a pulse train separated by 443 ns, the estimated sample temperature at the delay time was above 1400 K, confirmed by in situ ransformation of α- to γ-iron. Ultimately, the Fe and N 2 reacted uniformly throughout the beam path to form Fe 3 N 1.33 , as deduced from its established equation of state (EOS). We thus demonstrate that the activation energy provided by intense X-ray exposures in an XFEL can be coupled with the source time structure to enable exploration of the time-dependence of reactions under high-pressure conditions.

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