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Electrochemically Induced Metallization of NaCl: Use of the Main Component of Salt as a Cost-Effective Electrode Material for Sodium-Ion Batteries AITranslate

Korea University of Science and Technology; Korea University of Science and Technology; Korea University; Korea University of Science and Technology; Korea University of Science and Technology
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Publisher: ACS
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Abstract AITranslate

Sodium chloride (NaCl), a typical stoichiometric ionic compound, breaks all of the basic rules of chemistry at high pressures and can form new metallic compounds with different stoichiometries of NaxCl at x > 1. However, the electrochemical phase transition of NaCl from an insulating state to a metallic state without pressurization has not been achieved to date. In this study, we first demonstrate that nonmetallic NaCl can be transformed to a metallic compound through an electrochemical activation process. Subsequently, the activated NaCl electrode was shown to intercalate/deintercalate sodium ions into the structure, with a discharge capacity of 267 mAh/g by reversibly accommodating 0.6 Na ions. We believe that this method may represent a new approach for designing inexpensive electrode materials using the main component of table and sea salt for sodium-ion batteries. In addition, these results will contribute to the development of low-cost and sustainable rechargeable batteries that can be operated at a room temperature.

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DOI:https://doi.org/10.1021/acsenergylett.9b01118

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Citation Information:

Sodium chloride (NaCl), a typical stoichiometric ionic compound, breaks all of the basic rules of chemistry at high pressures and can form new metallic compounds with different stoichiometries of NaxCl at x > 1. However, the electrochemical phase transition of NaCl from an insulating state to a metallic state without pressurization has not been achieved to date. In this study, we first demonstrate that nonmetallic NaCl can be transformed to a metallic compound through an electrochemical activation process. Subsequently, the activated NaCl electrode was shown to intercalate/deintercalate sodium ions into the structure, with a discharge capacity of 267 mAh/g by reversibly accommodating 0.6 Na ions. We believe that this method may represent a new approach for designing inexpensive electrode materials using the main component of table and sea salt for sodium-ion batteries. In addition, these results will contribute to the development of low-cost and sustainable rechargeable batteries that can be operated at a room temperature.

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GB/T 7714-2015 [1] Iqra Moeez, HeeDae Lim, JaeHo Park, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.9b01118.
MLA [1] Iqra Moeez, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.9b01118.
APA [1] Iqra Moeez, HeeDae Lim, JaeHo Park, HunGi Jung, & Kyung Yoon Chung. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.9b01118
IEEE [1] Iqra Moeez, HeeDae Lim, JaeHo Park, HunGi Jung, and Kyung Yoon Chung, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.9b01118.