4.7 Article

A first-principles study of helium diffusion in quartz and coesite under high pressure up to 12GPa

Journal

GEOSCIENCE FRONTIERS
Volume 12, Issue 2, Pages 1001-1009

Publisher

CHINA UNIV GEOSCIENCES, BEIJING
DOI: 10.1016/j.gsf.2020.09.009

Keywords

Helium; Diffusion; Quartz; Coesite; High pressure

Funding

  1. National Natural Science Foundation of China [41174071, 41573121]
  2. United Laboratory of High-Pressure Physics and Earthquake Science [2019HPPES06, 2019HPPES07]
  3. Special Found of the Institute of Earthquake Forecasting, China Earthquake Administration [2018IEF010204]
  4. Key Laboratory of Earthquake Prediction, Institute pf Earthquake Forecasting, China Earthquake Administration [2017KLEP03]

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This study reports helium incorporation and diffusion mechanism in quartz and coesite, revealing anisotropic diffusion of helium in both minerals and increased activation energies under high pressure. Helium cannot be quantitatively retained in silica at typical Earth surface temperatures, which has implications for the discussion of mantle evolution and recognition of thermal histories of ultra-high pressure metamorphic terranes.
Helium diffusion in mantle minerals is crucial for understanding mantle structure and the dynamic processes of Earth's degassing. In this paper, we report helium incorporation and the mechanism of its diffusion in perfect crystals of quartz and coesite. The diffusion pathways, activation energies (E-a), and frequency factors of helium under ambient and high pressure conditions were calculated using Density Functional Theory (NT) and the climbing image nudged elastic band (CI-NEB) method. The calculated diffusive coefficients of He in the quartz in different orientations are: D[100] = 1.24 x 10(-6) exp. (-26.83 kJ / mol / RT) m(2) /s D[010] = 1.11 x 10(-6) exp. (-31.60 kJ / mol / RT) m(2)/s and in the coesite: D[100] = 3.00 x 10(-7) exp. (-33.79 kJ / mol / RT) m(2)/s D[001] = 2.21 x 10(-6) exp. (-18.33 kJ / mol / RT) m(2)/s The calculated results indicate that diffusivity of helium is anisotropic in both quartz and coesite and that the degree of anisotropy is much more pronounced in coesite. Helium diffusion behavior in coesite under high pressures was investigated. The activation energies increased with pressure: E-a[100] increased from 33.79 kJ/mol to 58.36 kJ/mol, and E-a[001] increased from 18.33 kJ/mol to 48.87 kJ/mol as pressure increased from 0 GPa to 12 GPa Our calculations showed that helium is not be quantitatively retained in silica at typical surface temperatures on Earth, which is consistent with the findings from previous studies. These results have implications for discussion of the Earth's mantle evolution and for recognition thermal histories of ultra-high pressure (UHP) metamorphic terranes. (C) 2020 Elsevier B.V.

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