journal article·2020-01Open access

Elucidating the role of anionic chemistry towards high-rate intermediate-temperature Na-metal halide batteries

Xiaowen Zhan, Jonathan P. Sepulveda, Xiaochuan Lu, Jeff F. Bonnett, Nathan L. Canfield, Teresa Lemmon, Keeyoung Jung, David M. Reed, Vincent L. Sprenkle, Guosheng Li

Abstract

Abstract Sodium (Na)-based battery technologies that are economical (because Na is abundant) and have long cycle life are gaining importance for large-scale energy storage applications. Among the widely studied Na-based battery systems, intermediate-temperature (IT) Na-metal halide (Na-MH) batteries have demonstrated several advantages over conventional high-temperature Na batteries, including superior battery safety, lower operating temperature and manufacturing cost, potentially longer cycle life, and easier assembly. However, the rate performance of IT Na-MH batteries is inevitably affected by the lower operating temperatures. In pursuit of faster charge-transfer reaction kinetics, we extended our studies of cathode materials beyond the extensively investigated NiCl2 to NiBr2 (NaBr/Ni) and NiI2 (NaI/Ni) compounds. We systematically investigated the synergetic effects of anion chemistry on the electrochemical properties. Surprisingly, among three tested cathodes, the NaBr/Ni cathode showed the highest energy density of 174 Wh/kg at 33.3 mA/cm2 (∼0.8C), which is 2.5 and 1.9 times higher than those of NaCl/Ni and NaI/Ni cells. We explored the underlying enhancement mechanism in great detail via multiple structural characterization and electrochemical techniques. The sodium-halide salt dissolution in molten NaAlCl4 was found to be the determining factor in rate improvement. Our findings will greatly advance IT Na-MH battery technologies and pave the way towards fundamental understanding of reaction kinetics for high-temperature batteries in general.
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Research context

OpenAlex topics: Advanced Battery Materials and Technologies · Thermal Expansion and Ionic Conductivity · Advancements in Battery Materials

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