4.3 Article

Inner-shell chemistry under high pressure

Journal

JAPANESE JOURNAL OF APPLIED PHYSICS
Volume 56, Issue 5, Pages -

Publisher

IOP PUBLISHING LTD
DOI: 10.7567/JJAP.56.05FA10

Keywords

-

Funding

  1. MRSEC program [NSF-DMR1121053]
  2. ConvEne-IGERT Program [NSF-DGE 0801627]
  3. CNSI
  4. MRL
  5. NSF [CNS-0960316, TG-DMR130005]
  6. Department of Energy National Nuclear Security Administration (DOE-NNSA) [DE-NA0002912]
  7. DOE [DE-FC08-01NV14049]
  8. University of Nevada, Las Vegas
  9. DOE-NNSA [DE-NA0001974]
  10. DOE-BES [DE-FG02-99ER45775, DE-AC02-06CH11357]
  11. NSF

Ask authors/readers for more resources

Chemistry at ambient conditions has implicit boundaries rooted in the atomic shell structure: the inner-shell electrons and the unoccupied outer-shell orbitals do not contribute as the major component to chemical reactions and in chemical bonds. These general rules govern our understanding of chemical structures and reactions. We review the recent progresses in high-pressure chemistry demonstrating that the above rules can be violated under extreme conditions. Using a first principles computation method and crystal structure search algorithm, we demonstrate that stable compounds involving inner shell electrons such as CsF3, CsF5, HgF3, and HgF4 can form under high external pressure and may present exotic properties. We also discuss experimental studies that have sought to confirm these predictions. Employing our recently developed hard X-ray photochemistry methods in a diamond anvil cell, we show promising early results toward realizing inner shell chemistry experimentally. (C) 2017 The Japan Society of Applied Physics

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