journal article·2024-07-04Open access

Synthesis and Properties of the Helium Clathrate and Defect Perovskite [He2–x□x][CaNb]F6

Shangye Ma, Brett R. Hester, Anthony J. Lloyd, Antonio M. dos Santos, Jamie J. Molaison, Angus P. Wilkinson

The Journal of Physical Chemistry C· Volume 128· Issue 26

Abstract

High Resolution Image Download MS PowerPoint Slide The defect double perovskite [He 2– x □ x ][CaNb]F 6, with helium on its A-site, can be prepared by the insertion of helium into ReO 3 -type CaNbF 6 at high pressure. Upon cooling from 300 to 100 K under 0.4 GPa helium, ∼60% of the A-sites become occupied. Helium uptake was quantified by both neutron powder diffraction and gas insertion and release measurements. After the conversion of gauge pressure to fugacity, the uptake of helium by CaNbF 6 can be described by a Langmuir isotherm. The enthalpy of absorption for helium in [He 2– x □ x ][CaNb]F 6 is estimated to be ∼+3(1) kJ mol –1, implying that its formation is entropically favored. Helium is able to diffuse through the material on a time scale of minutes at temperatures down to ∼150 K but is trapped at 100 K and below. The insertion of helium into CaNbF 6 reduces the magnitude of its negative thermal expansion, increases the bulk modulus, and modifies its phase behavior. On compressing pristine CaNbF 6, at 50 and 100 K, a cubic (Fm3̅m) to rhombohedral (R3̅) phase transition was observed at <0.20 GPa. However, a helium-containing sample remained cubic at 0.4 GPa and 50 K. CaNbF 6, compressed in helium at room temperature, remained cubic to >3.7 GPa, the limit of our X-ray diffraction measurements, in contrast to prior reports that upon compression in a nonpenetrating medium, a phase transition is detected at ∼0.4 GPa.
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Research context

OpenAlex topics: Thermal Expansion and Ionic Conductivity · Magnetic and transport properties of perovskites and related materials · Inorganic Fluorides and Related Compounds

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332-0400, United States

Neutron Scattering Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States

School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0245, United States

Funding

Division of Materials Research

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