Logo del repository
  1. Home
 
Opzioni

Collective spin 1 singlet phase in high-pressure oxygen

Crespo, Yanier
•
Fabrizio, Michele
•
Scandolo, Sandro
•
Tosatti, Erio
2014
  • journal article

Periodico
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Abstract
Oxygen, one of the most common and important elements in nature, has an exceedingly well-explored phase diagram under pressure, up to and beyond 100 GPa. At low temperatures, the low-pressure antiferromagnetic phases below 8 GPa where O-2 molecules have spin S = 1 are followed by the broad apparently nonmagnetic epsilon phase from about 8 to 96 GPa. In this phase, which is our focus, molecules group structurally together to form quartets while switching, as believed by most, to spin S = 0. Here we present theoretical results strongly connecting with existing vibrational and optical evidence, showing that this is true only above 20 GPa, whereas the S = 1 molecular state survives up to about 20 GPa. The epsilon phase thus breaks up into two: a spinless epsilon(0) (20-96 GPa), and another epsilon(1) (8-20 GPa) where the molecules have S = 1 but possess only short-range antiferromagnetic correlations. A local spin liquid-like singlet ground state akin to some earlier proposals, and whose optical signature we identify in existing data, is proposed for this phase. Our proposed phase diagram thus has a first-order phase transition just above 20 GPa, extending at finite temperature and most likely terminating into a crossover with a critical point near 30 GPa and 200 K.
DOI
10.1073/pnas.1404590111
WOS
WOS:000339310700023
Archivio
http://hdl.handle.net/20.500.11767/30184
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84924399861
https://arxiv.org/abs/1409.4956
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4115506/
https://arxiv.org/abs/1409.4956
Diritti
closed access
Soggetti
  • Density functional

  • IR mode

  • Molecular magnetism

  • Raman mode

  • Tetramer

  • Settore FIS/03 - Fisi...

Web of Science© citazioni
20
Data di acquisizione
Mar 22, 2024
Visualizzazioni
1
Data di acquisizione
Apr 19, 2024
Vedi dettagli
google-scholar
Get Involved!
  • Source Code
  • Documentation
  • Slack Channel
Make it your own

DSpace-CRIS can be extensively configured to meet your needs. Decide which information need to be collected and available with fine-grained security. Start updating the theme to match your nstitution's web identity.

Need professional help?

The original creators of DSpace-CRIS at 4Science can take your project to the next level, get in touch!

Realizzato con Software DSpace-CRIS - Estensione mantenuta e ottimizzata da 4Science

  • Impostazioni dei cookie
  • Informativa sulla privacy
  • Accordo con l'utente finale
  • Invia il tuo Feedback