Search NASA⌕ Search

DOE OSTI · 1287506

Materials Data on Yb6Cl13 by Materials Project

Abstract

Yb6Cl13 is Baddeleyite-like structured and crystallizes in the triclinic P-1 space group. The structure is three-dimensional. there are six inequivalent Yb+2.17+ sites. In the first Yb+2.17+ site, Yb+2.17+ is bonded to seven Cl1- atoms to form a mixture of distorted corner and edge-sharing YbCl7 pentagonal bipyramids. There are a spread of Yb–Cl bond distances ranging from 2.74–2.87 Å. In the second Yb+2.17+ site, Yb+2.17+ is bonded in a 7-coordinate geometry to eight Cl1- atoms. There are a spread of Yb–Cl bond distances ranging from 2.73–3.31 Å. In the third Yb+2.17+ site, Yb+2.17+ is bonded to seven Cl1- atoms to form a mixture of distorted corner and edge-sharing YbCl7 pentagonal bipyramids. There are a spread of Yb–Cl bond distances ranging from 2.75–2.86 Å. In the fourth Yb+2.17+ site, Yb+2.17+ is bonded to seven Cl1- atoms to form a mixture of distorted corner and edge-sharing YbCl7 pentagonal bipyramids. There are a spread of Yb–Cl bond distances ranging from 2.78–2.92 Å. In the fifth Yb+2.17+ site, Yb+2.17+ is bonded to seven Cl1- atoms to form a mixture of distorted corner and edge-sharing YbCl7 pentagonal bipyramids. There are a spread of Yb–Cl bond distances ranging from 2.76–2.95 Å. In the sixth Yb+2.17+ site, Yb+2.17+ is bonded in a 8-coordinate geometry to eight Cl1- atoms. There are a spread of Yb–Cl bond distances ranging from 2.73–3.20 Å. There are thirteen inequivalent Cl1- sites. In the first Cl1- site, Cl1- is bonded to four Yb+2.17+ atoms to form a mixture of distorted corner and edge-sharing ClYb4 tetrahedra. In the second Cl1- site, Cl1- is bonded in a distorted trigonal planar geometry to three Yb+2.17+ atoms. In the third Cl1- site, Cl1- is bonded in a distorted trigonal non-coplanar geometry to three Yb+2.17+ atoms. In the fourth Cl1- site, Cl1- is bonded in a distorted trigonal non-coplanar geometry to three Yb+2.17+ atoms. In the fifth Cl1- site, Cl1- is bonded in a distorted trigonal planar geometry to three Yb+2.17+ atoms. In the sixth Cl1- site, Cl1- is bonded to four Yb+2.17+ atoms to form a mixture of distorted corner and edge-sharing ClYb4 tetrahedra. In the seventh Cl1- site, Cl1- is bonded in a distorted trigonal planar geometry to three Yb+2.17+ atoms. In the eighth Cl1- site, Cl1- is bonded to four Yb+2.17+ atoms to form a mixture of distorted corner and edge-sharing ClYb4 tetrahedra. In the ninth Cl1- site, Cl1- is bonded in a 2-coordinate geometry to three Yb+2.17+ atoms. In the tenth Cl1- site, Cl1- is bonded to four Yb+2.17+ atoms to form a mixture of distorted corner and edge-sharing ClYb4 tetrahedra. In the eleventh Cl1- site, Cl1- is bonded in a 3-coordinate geometry to three Yb+2.17+ atoms. In the twelfth Cl1- site, Cl1- is bonded to four Yb+2.17+ atoms to form a mixture of corner and edge-sharing ClYb4 tetrahedra. In the thirteenth Cl1- site, Cl1- is bonded in a distorted trigonal planar geometry to three Yb+2.17+ atoms.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

2020-07-15. Materials Data on Yb6Cl13 by Materials Project. https://doi.org/10.17188/1287506

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related reports

Cyclic moisture reactivation of calcium sorbents for long duration thermochemical energy storage

The transition to a flexible and reliable energy infrastructure, using electro-thermal energy generation technologies such as geothermal, concentrated solar power, and nuclear, usually demands simultaneous advancement of thermal energy storage (TES) to support on-demand electricity generation and industrial applications while mitigating the inherent intermittency of renewable energy sources and power outages from direct energy generation. Among TES technologies, thermochemical energy storage (TCES) based on calcium looping emerges as a compelling high-power energy storage candidate due to its high reaction enthalpy, compatibility with elevated operating temperatures, and abundance of low-cost materials. However, the long-term durability of calcium-based sorbents for TCES is hindered by surface sintering and particle aggregation, leading to performance degradation over repeated thermal cycles. This study explores a moisture hydration-based strategy to regenerate a degraded calcium sorbent and mitigate performance degradation for long duration TCES. The addition of moisture transforms calcium oxide into calcium hydroxide and produces intercalation water layers, associated with a regenerated surface area and reduced calcium oxide crystallite size. Both these effects are beneficial in restoring the sorbents' reactivity for carbonization. Additionally, an optimized hydration-assisted reactivation protocol balances the recovered energy storage capacity with heating penalty required for moisture removal from hydrated samples, resulting in an enhanced energy storage capacity up to 176% compared to benchmark sorbents that undergo cycling without reactivation after 60 cycles. In conclusion, these results highlight the potential of hydration-assisted reactivation to enhance the long-term performance of TCES, providing an effective pathway to advancing electro-thermal storage technologies.

36 MATERIALS SCIENCE↗