Raman studies of hydrogen trapped in As4O6·2H2 at high pressure and low temperature
- Warsaw Univ. of Technology (Poland); Carnegie Inst. for Science, Washington, DC (United States)
- Carnegie Inst. for Science, Washington, DC (United States)
- Warsaw Univ. of Technology (Poland)
In this work, Raman spectroscopic measurements of the arsenolite–hydrogen inclusion compound As4O6·2H2 were performed in diamond anvil cells at high pressure and variable temperature down to 80 K. The experimental results were complemented by ab initio molecular dynamics simulations and phonon calculations. Observation of three hydrogen vibrons in As4O6·2H2 is reported in the entire temperature and pressure range studied (up to 24 GPa). While the experiments performed with protium and deuterium at variable temperatures allowed for the assignment of two vibrons as Q1(1) and Q1(0) transitions of ortho and para spin isomers of hydrogen trapped in the inclusion compound, the origin of the third vibron could not be unequivocally established. Low-temperature spectra revealed that the lowest-frequency vibron is actually composed of two overlapping bands of Ag and T2g symmetries dominated by H2 stretching modes as predicted by our previous density functional theory calculations. We observed low-frequency modes of As4O6·2H2 vibrations dominated by H2 “librations,” which were missed in a previous study. A low-temperature fine structure was observed for the J = 0 → 2 and J = 1 → 3 manifolds of hydrogen trapped in As4O6·2H2, indicating the lifting of degeneracy due to an anisotropic environment. A non-spherical distribution was captured by molecular dynamics simulations, which revealed that the trajectory of H2 molecules is skewed along the crystallographic $$\langle$$111$$\rangle$$ direction. Last but not least, low-temperature synchrotron powder x-ray diffraction measurements on As4O6·2H2 revealed that the bulk structure of the compound is preserved down to 5 K at 1.6 GPa.
- Research Organization:
- Argonne National Laboratory (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
- Sponsoring Organization:
- Polish National Agency for Academic Exchange (NAWA); US Army Research Office (ARO); USDOE National Nuclear Security Administration (NNSA); USDOE Office of Science (SC)
- Grant/Contract Number:
- 260; W911NF-17-1-0604; AC02-06CH11357
- OSTI ID:
- 1647377
- Alternate ID(s):
- OSTI ID: 1644369
- Journal Information:
- Journal of Chemical Physics, Vol. 153, Issue 5; ISSN 0021-9606
- Publisher:
- American Institute of Physics (AIP)Copyright Statement
- Country of Publication:
- United States
- Language:
- ENGLISH
Web of Science
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