Search NASA⌕ Search

DOE OSTI · 1201100

Materials Data on UGe3 by Materials Project

Abstract

UGe3 is Uranium Silicide structured and crystallizes in the cubic Pm-3m space group. The structure is three-dimensional. U is bonded to twelve equivalent Ge atoms to form UGe12 cuboctahedra that share corners with twelve equivalent UGe12 cuboctahedra, edges with twenty-four equivalent GeU4Ge8 cuboctahedra, faces with six equivalent UGe12 cuboctahedra, and faces with twelve equivalent GeU4Ge8 cuboctahedra. All U–Ge bond lengths are 2.97 Å. Ge is bonded to four equivalent U and eight equivalent Ge atoms to form distorted GeU4Ge8 cuboctahedra that share corners with twelve equivalent GeU4Ge8 cuboctahedra, edges with eight equivalent UGe12 cuboctahedra, edges with sixteen equivalent GeU4Ge8 cuboctahedra, faces with four equivalent UGe12 cuboctahedra, and faces with fourteen equivalent GeU4Ge8 cuboctahedra. All Ge–Ge bond lengths are 2.97 Å.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

2020-07-16. Materials Data on UGe3 by Materials Project. https://doi.org/10.17188/1201100

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↗