Advanced Na-NiCl2 Battery Using Nickel-Coated Graphite with Core–Shell Microarchitecture
Source abstract
Abstract
Stationary electric energy storage devices (rechargeable batteries) have gained increasing prominence due to great market needs, such as smoothing the fluctuation of renewable energy resources and supporting the reliability of the electric grid. With regard to raw materials availability, sodium-based batteries are better positioned than lithium batteries due to the abundant resource of sodium in Earth’s crust. However, the sodium–nickel chloride (Na-NiCl 2 ) battery, one of the most attractive stationary battery technologies, is hindered from further market penetration by its high material cost (Ni cost) and fast material degradation at its high operating temperature. Here, we demonstrate the design of a core–shell microarchitecture, nickel-coated graphite, with a graphite core to maintain electrochemically active surface area and structural integrity of the electron percolation pathway while using 40% less Ni than conventional Na-NiCl 2 batteries. An initial energy density of 133 Wh/kg (at ∼C/4) and energy efficiency of 94% are achieved at an intermediate temperature of 190 °C.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Stationary Energy Storage Group, Energy and Environmental Directorate, Pacific Northwest National Laboratory, Richland, Washington 99352, United States
Materials Research Division, Research Institute of Industrial Science & Technology (RIST), Pohang 37673, Republic of Korea
Funding
Research and Development · Korea Institute of Energy Technology Evaluation and Planning
References (23)
Show source-provided references
1. 10.1146/annurev-chembioeng-061010-11411610.1146/annurev-chembioeng-061010-114116 ↗
2. 10.1021/cr100290v10.1021/cr100290v ↗
3. 10.1126/science.121274110.1126/science.1212741 ↗
4. 10.1016/j.jpowsour.2009.11.12010.1016/j.jpowsour.2009.11.120 ↗
5. 10.1002/cphc.20140221510.1002/cphc.201402215 ↗
6. Sudworth J. L. · 1985
7. 10.1039/c3ee24086j10.1039/c3ee24086j ↗
8. 10.1002/adfm.20120047310.1002/adfm.201200473 ↗
9. 10.1016/0378-7753(94)01967-310.1016/0378-7753(94)01967-3 ↗
10. 10.1016/j.jpowsour.2003.09.03910.1016/j.jpowsour.2003.09.039 ↗
11. 10.1149/1.208614710.1149/1.2086147 ↗
12. 10.1149/1.281194410.1149/1.2811944 ↗
13. 10.1002/aenm.20150035710.1002/aenm.201500357 ↗
14. 10.1039/c3ee24244g10.1039/c3ee24244g ↗
15. 10.1149/2.0421503jes10.1149/2.0421503jes ↗
16. 10.1016/j.jpowsour.2012.05.02010.1016/j.jpowsour.2012.05.020 ↗
17. 10.1016/j.jpowsour.2013.10.11010.1016/j.jpowsour.2013.10.110 ↗
18. 10.1038/ncomms557810.1038/ncomms5578 ↗
19. 10.1038/ncomms1068310.1038/ncomms10683 ↗
20. 10.1039/c3ta13644b10.1039/c3ta13644b ↗
21. Galloway R. C. · 2003
22. Virkar, A. V.; Jue, J.F.; Fung, K.Z.Alkali-metal-β- and β″-alumina and Gallate Polycrystalline Ceramics and Fabrication by a Vapor Phase Method. U.S. Patent 6,117,807 A, 1998.
23. 10.1038/nenergy.2016.1010.1038/nenergy.2016.10 ↗