Search NASA⌕ Search

DOE OSTI · 1318177

Materials Data on Ca3(CuO3)2 by Materials Project

Abstract

Ca3Cu2O6 crystallizes in the monoclinic Cm space group. The structure is three-dimensional. there are three inequivalent Ca2+ sites. In the first Ca2+ site, Ca2+ is bonded in a 7-coordinate geometry to seven O2- atoms. There are a spread of Ca–O bond distances ranging from 2.29–2.57 Å. In the second Ca2+ site, Ca2+ is bonded in a 7-coordinate geometry to seven O2- atoms. There are a spread of Ca–O bond distances ranging from 2.21–2.61 Å. In the third Ca2+ site, Ca2+ is bonded to seven O2- atoms to form distorted edge-sharing CaO7 hexagonal pyramids. There are a spread of Ca–O bond distances ranging from 2.36–2.50 Å. There are two inequivalent Cu3+ sites. In the first Cu3+ site, Cu3+ is bonded in a square co-planar geometry to four O2- atoms. There are a spread of Cu–O bond distances ranging from 1.82–1.95 Å. In the second Cu3+ site, Cu3+ is bonded in a square co-planar geometry to four O2- atoms. There are a spread of Cu–O bond distances ranging from 1.82–1.89 Å. There are six inequivalent O2- sites. In the first O2- site, O2- is bonded to three Ca2+ and two equivalent Cu3+ atoms to form distorted OCa3Cu2 trigonal bipyramids that share a cornercorner with one OCa5Cu octahedra, corners with four equivalent OCa4Cu square pyramids, corners with three OCa3Cu2 trigonal bipyramids, an edgeedge with one OCa3Cu2 trigonal bipyramid, and faces with two equivalent OCa5Cu octahedra. The corner-sharing octahedral tilt angles are 39°. In the second O2- site, O2- is bonded to three Ca2+ and two equivalent Cu3+ atoms to form distorted OCa3Cu2 trigonal bipyramids that share corners with five equivalent OCa5Cu octahedra, corners with three OCa3Cu2 trigonal bipyramids, an edgeedge with one OCa3Cu2 trigonal bipyramid, and faces with two equivalent OCa4Cu square pyramids. The corner-sharing octahedra tilt angles range from 39–64°. In the third O2- site, O2- is bonded to four Ca2+ and one Cu3+ atom to form distorted OCa4Cu square pyramids that share corners with four equivalent OCa5Cu octahedra, corners with four equivalent OCa3Cu2 trigonal bipyramids, edges with two equivalent OCa5Cu octahedra, edges with two equivalent OCa4Cu square pyramids, and faces with two equivalent OCa3Cu2 trigonal bipyramids. The corner-sharing octahedra tilt angles range from 5–6°. In the fourth O2- site, O2- is bonded to five Ca2+ and one Cu3+ atom to form distorted OCa5Cu octahedra that share corners with four equivalent OCa4Cu square pyramids, corners with six OCa3Cu2 trigonal bipyramids, edges with two equivalent OCa5Cu octahedra, edges with two equivalent OCa4Cu square pyramids, and faces with two equivalent OCa3Cu2 trigonal bipyramids. In the fifth O2- site, O2- is bonded in a distorted see-saw-like geometry to three Ca2+ and one Cu3+ atom. In the sixth O2- site, O2- is bonded in a distorted rectangular see-saw-like geometry to three Ca2+ and one Cu3+ atom.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

2020-07-22. Materials Data on Ca3(CuO3)2 by Materials Project. https://doi.org/10.17188/1318177

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↗