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Title: Possible H2O storage in the crystal structure of CaSiO3 perovskite

Journal Article · · Physics of the Earth and Planetary Interiors
 [1];  [1];  [2];  [3];  [4];  [5];  [5];  [1]
  1. Arizona State Univ., Tempe, AZ (United States)
  2. Univ. of Chicago, IL (United States)
  3. Univ. of Chicago, IL (United States); Deutsches Elektronen-Synchrotron (DESY), Hamburg (Germany)
  4. Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
  5. Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Advanced Light Source (ALS)

The lower mantle is believed to contain much less hydrogen (or H2O) because of the low storage capacity of the dominant mineral phases, such as bridgmanite and ferropericlase. However, possible hydrogen storage in the third most abundant mineral in the region, CaSiO3 perovskite (Ca-Pv), is not well unknown. Here, we have synthesized Ca-Pv from different starting materials with varying H2O contents at 19–120 GPa and 1400–2200 K in laser-heated diamond-anvil cell. While cubic perovskite structure is stable at the mantle-related pressures-temperatures (P-T) in anhydrous systems, we found non-cubic diffraction peak splitting in Ca-Pv even at high temperatures when it is synthesized from hydrous starting materials. In-situ high-pressure infrared spectroscopy showed OH vibration possibly from Ca-Pv. The unit-cell volume of hydrothermally synthesized Ca-Pv is systematically smaller than that of anhydrous Ca-Pv at high pressures. These observations suggest possible H2O storage in Ca-Pv at mantle-related P-T conditions. We also found the formation of separate δ–AlOOH and Ca-Pv phases from Al-bearing CaSiO3 glass starting materials in an H2O medium at 60 GPa and 1400 K. Ca-Pv still showed non-cubic peak splitting at high temperatures in this experiment. Therefore, it is possible that hydrous phases may coexist together with hydrous Ca-Pv in the lower mantle.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities Division; USDOE National Nuclear Security Administration (NNSA); National Science Foundation (NSF); National Aeronautics and Space Administration (NASA)
Grant/Contract Number:
AC02-06CH11357; AC02-05CH11231; EAR1338810; 80NSSC18K0353; EAR-1228799; FG02-94ER14466; NA0001974; FG02-99ER45775
OSTI ID:
1756050
Alternate ID(s):
OSTI ID: 1702138
Journal Information:
Physics of the Earth and Planetary Interiors, Vol. 299; ISSN 0031-9201
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English

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