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Synchrotron infrared spectroscopic evidence of the probable transition to metal hydrogen

Author

Listed:
  • Paul Loubeyre

    (CEA, DAM, DIF)

  • Florent Occelli

    (CEA, DAM, DIF)

  • Paul Dumas

    (CEA, DAM, DIF
    Synchrotron SOLEIL)

Abstract

Hydrogen has been an essential element in the development of atomic, molecular and condensed matter physics1. It is predicted that hydrogen should have a metal state2; however, understanding the properties of dense hydrogen has been more complex than originally thought, because under extreme conditions the electrons and protons are strongly coupled to each other and ultimately must both be treated as quantum particles3,4. Therefore, how and when molecular solid hydrogen may transform into a metal is an open question. Although the quest for metal hydrogen has pushed major developments in modern experimental high-pressure physics, the various claims of its observation remain unconfirmed5–7. Here a discontinuous change of the direct bandgap of hydrogen, from 0.6 electronvolts to below 0.1 electronvolts, is observed near 425 gigapascals. This result is most probably associated with the formation of the metallic state because the nucleus zero-point energy is larger than this lowest bandgap value. Pressures above 400 gigapascals are achieved with the recently developed toroidal diamond anvil cell8, and the structural changes and electronic properties of dense solid hydrogen at 80 kelvin are probed using synchrotron infrared absorption spectroscopy. The continuous downward shifts of the vibron wavenumber and the direct bandgap with increased pressure point to the stability of phase-III hydrogen up to 425 gigapascals. The present data suggest that metallization of hydrogen proceeds within the molecular solid, in good agreement with previous calculations that capture many-body electronic correlations9.

Suggested Citation

  • Paul Loubeyre & Florent Occelli & Paul Dumas, 2020. "Synchrotron infrared spectroscopic evidence of the probable transition to metal hydrogen," Nature, Nature, vol. 577(7792), pages 631-635, January.
  • Handle: RePEc:nat:nature:v:577:y:2020:i:7792:d:10.1038_s41586-019-1927-3
    DOI: 10.1038/s41586-019-1927-3
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    Cited by:

    1. M. I. Eremets & V. S. Minkov & P. P. Kong & A. P. Drozdov & S. Chariton & V. B. Prakapenka, 2023. "Universal diamond edge Raman scale to 0.5 terapascal and implications for the metallization of hydrogen," Nature Communications, Nature, vol. 14(1), pages 1-8, December.
    2. Kejun Bu & Qingyang Hu & Xiaohuan Qi & Dong Wang & Songhao Guo & Hui Luo & Tianquan Lin & Xiaofeng Guo & Qiaoshi Zeng & Yang Ding & Fuqiang Huang & Wenge Yang & Ho-Kwang Mao & Xujie Lü, 2022. "Nested order-disorder framework containing a crystalline matrix with self-filled amorphous-like innards," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    3. Mianzhen Mo & Minxue Tang & Zhijiang Chen & J. Ryan Peterson & Xiaozhe Shen & John Kevin Baldwin & Mungo Frost & Mike Kozina & Alexander Reid & Yongqiang Wang & Juncheng E & Adrien Descamps & Benjamin, 2022. "Ultrafast visualization of incipient plasticity in dynamically compressed matter," Nature Communications, Nature, vol. 13(1), pages 1-8, December.

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