4.8 Article

Origin of Pressure-Induced Polyamorphism in Ce75Al25 Metallic Glass

期刊

PHYSICAL REVIEW LETTERS
卷 104, 期 10, 页码 -

出版社

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.104.105702

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资金

  1. U.S. Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences (BES) [DE-SC0001057]
  2. DOE-BES [DE-AC02-06CH11357]
  3. DOE-NNSA (CDAC)
  4. NSF
  5. Natural Sciences and Engineering Research Council of Canada, University of Washington
  6. Simon Fraser University
  7. APS
  8. Balzan Foundation, National Natural Science Foundation of China [50601021, 50701038, 60776014, 60876002, 50920105101, 10979002]
  9. Zhejiang University-Helmholtz Cooperation Fund
  10. Ministry of Education of China
  11. Doctoral Education Foundation
  12. China State Oversea Foundation
  13. Department of Science and Technology of Zhejiang Province
  14. Baoyugang Foundation of Zhejiang University

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Using high-pressure synchrotron x-ray absorption spectroscopy, we observed the Ce 4f electron in Ce75Al25 metallic glass transform from its ambient localized state to an itinerant state above 5 GPa. A parallel x-ray diffraction study revealed a volume collapse of about 8.6%, coinciding with 4f delocalization. The transition started from a low-density state below 1.5 GPa, went through continuous densification ending with a high-density state above 5 GPa. This new type of electronic polyamorphism in densely packed metallic glass is dictated by the Ce constituent, and is fundamentally distinct from the well-established structural polyamorphism in which densification is caused by coordination change and atomic rearrangement.

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