Engineering Papers⌕ Search
Home/Archive/DOE OSTI

DOE OSTI · 1730671

Materials Data on FeNiTe4 by Materials Project

View original source ↗Read source document ↗Export metadata ↓

Abstract

FeNiTe4 is pyrite-derived structured and crystallizes in the monoclinic P2_1/c space group. The structure is three-dimensional. Fe3+ is bonded to six Te+1.75- atoms to form FeTe6 octahedra that share corners with four equivalent FeTe6 octahedra and corners with eight equivalent NiTe6 octahedra. The corner-sharing octahedra tilt angles range from 60–63°. There are a spread of Fe–Te bond distances ranging from 2.54–2.59 Å. Ni4+ is bonded to six Te+1.75- atoms to form NiTe6 octahedra that share corners with four equivalent NiTe6 octahedra and corners with eight equivalent FeTe6 octahedra. The corner-sharing octahedra tilt angles range from 60–64°. There are four shorter (2.64 Å) and two longer (2.67 Å) Ni–Te bond lengths. There are two inequivalent Te+1.75- sites. In the first Te+1.75- site, Te+1.75- is bonded in a 3-coordinate geometry to one Fe3+ and two equivalent Ni4+ atoms. In the second Te+1.75- site, Te+1.75- is bonded in a 3-coordinate geometry to two equivalent Fe3+ and one Ni4+ atom.

Explore related subjects

36 MATERIALS SCIENCEcrystal structureFe-Ni-TeFeNiTe4

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

2020-05-02. Materials Data on FeNiTe4 by Materials Project. https://doi.org/10.17188/1730671

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

KEEP EXPLORING

Related reports

DOE OSTI2026

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↗