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Reversible devitrification in amorphous As2 Se3 under pressure

  • Azkar Saeed Ahmad
  • , Hong Bo Lou
  • , Chuan Long Lin
  • , Ai Guo Li
  • , Ke Yang
  • , K. Glazyrin
  • , H. P. Liermann
  • , Hermann Franz
  • , Kenny Ståhl
  • , Shuo Cui
  • , Bruno Bureau
  • , Dong-Xian Zhang
  • , Xiao-Dong Wang
  • , Qing-Ping Cao
  • , A. Lindsay Greer
  • , Jian-Zhong Jiang
  • Zhejiang University
  • Chinese Academy of Sciences
  • German Electron Synchrotron
  • Université de Rennes
  • University of Cambridge

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

In pressure-induced reversible structural transitions, the term "reversible" refers to the recovery of the virgin structure in a material upon complete decompression. Pressure-induced amorphous-to-crystalline transitions have been claimed to be reversible, but evidence that amorphous material recovers its virgin amorphous structure upon complete depressurization has been lacking. In amorphous As2Se3 (a-As2Se3) chalcogenide, however, we report a novel reversible amorphous-to-crystalline transition that provides compelling experimental evidence that upon complete decompression, the recovered amorphous phase is structurally the same as that of the virgin (as-cast) amorphous phase. Combining the experimental results with ab initio molecular dynamics simulations, we elucidate that the amorphization is mediated by a surplus of total free energy in the high-pressure face-centered cubic phase as compared to the virgin amorphous phase and that the structural recovery to the virgin amorphous phase is a consequence of an enhancement in covalent bonding character over interlayer forces upon complete decompression. Furthermore, we observed a two-dimensional to three-dimensional network transition under compression and its reversibility upon decompression.
Original languageEnglish
Article number195211
JournalPhysical Review B
Volume94
Issue number19
Number of pages7
ISSN2469-9950
DOIs
Publication statusPublished - 2016

Bibliographical note

©2016 American Physical Society

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