| dc.contributor.author | Ouchi, Takanari | |
| dc.contributor.author | Lambotte, Guillaume | |
| dc.contributor.author | Burke, Paul J. | |
| dc.contributor.author | Sadoway, Donald Robert | |
| dc.contributor.author | Spatocco, Brian Leonard | |
| dc.date.accessioned | 2016-04-07T15:55:13Z | |
| dc.date.available | 2016-04-07T15:55:13Z | |
| dc.date.issued | 2015-10 | |
| dc.date.submitted | 2015-09 | |
| dc.identifier.issn | 0013-4651 | |
| dc.identifier.issn | 1945-7111 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/102196 | |
| dc.description.abstract | The liquid metal battery (LMB) is attractive due to its simple construction, its circumvention of solid-state failure mechanisms and resultantly long lifetimes, and its particularly low levelized cost of energy. Here, we provide a study of a unique binary electrolyte, NaOH-NaI, in order to pursue a low-cost and low-temperature sodium-based liquid metal battery (LMB) for grid-scale electricity storage. Thermodynamic studies have confirmed a low eutectic melting temperature (220°C) as well as provided data to complete the phase diagram of this system. X-ray diffraction has further supported the existence of a recently discovered compound, Na[subscript 7](OH)[subscript 5]I[subscript 2], as well as offered initial evidence toward a NaI-rich compound displaying Pm-3m symmetry. These phase equilibrium data have then been used to optimize parameters from a two-sublattice thermodynamic solution model to provide a starting point for study of higher order systems. Further, a detailed electrochemical study has identified the voltage window and related oxidation/reduction reactions and found greatly improved stability of the pure sodium electrode against the electrolyte. Finally, an Na|NaOH-NaI|Pb-Bi proof-of-concept cell was assembled. This cell achieved over 100 cycles and displayed leakage currents below 0.40 mA/cm[superscript 2]. These results highlight an exciting class of low-melting molten salt electrolytes that may enable low cost grid-scale storage. | en_US |
| dc.description.sponsorship | United States. Advanced Research Projects Agency-Energy (Award DE-AR0000047) | en_US |
| dc.description.sponsorship | TOTAL (Firm) | en_US |
| dc.description.sponsorship | MIT Tata Center for Technology and Design | en_US |
| dc.language.iso | en_US | |
| dc.publisher | Electrochemical Society | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1149/2.0441514jes | en_US |
| dc.rights | Creative Commons Attribution | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_US |
| dc.source | Electrochemical Society | en_US |
| dc.title | Low-Temperature Molten Salt Electrolytes for Membrane-Free Sodium Metal Batteries | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | Spatocco, Brian L., Takanari Ouchi, Guillaume Lambotte, Paul J. Burke, and Donald R. Sadoway. “Low-Temperature Molten Salt Electrolytes for Membrane-Free Sodium Metal Batteries.” J. Electrochem. Soc. 162, no. 14 (2015): A2729–A2736. | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Materials Processing Center | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Materials Science and Engineering | en_US |
| dc.contributor.mitauthor | Spatocco, Brian L. | en_US |
| dc.contributor.mitauthor | Ouchi, Takanari | en_US |
| dc.contributor.mitauthor | Lambotte, Guillaume | en_US |
| dc.contributor.mitauthor | Sadoway, Donald Robert | en_US |
| dc.relation.journal | Journal of The Electrochemical Society | en_US |
| dc.eprint.version | Final published version | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dspace.orderedauthors | Spatocco, Brian L.; Ouchi, Takanari; Lambotte, Guillaume; Burke, Paul J.; Sadoway, Donald R. | en_US |
| dc.identifier.orcid | https://orcid.org/0000-0002-4921-9164 | |
| dc.identifier.orcid | https://orcid.org/0000-0003-1520-8552 | |
| mit.license | PUBLISHER_CC | en_US |
| mit.metadata.status | Complete | |