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The Effect of Supply Rate of Li Ion and Anion on Li Dissolution/Deposition Behavior in LiNO3 Electrolyte Solutions for Li-Air Batteries
Although Li-air batteries (LAB) have a high theoretical energy density (3500 Wh kg−1), further developments are required to overcome their practical limitations. Regarding the Li-metal negative electrode (NE), we have previously reported on the reversibility of the Li dissolution/deposition reaction...
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Published in: | Denki kagaku oyobi kōgyō butsuri kagaku 2024/04/20, Vol.92(4), pp.047003-047003 |
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description | Although Li-air batteries (LAB) have a high theoretical energy density (3500 Wh kg−1), further developments are required to overcome their practical limitations. Regarding the Li-metal negative electrode (NE), we have previously reported on the reversibility of the Li dissolution/deposition reaction by using Li|Li symmetric cells with a tetraglyme (G4)-based electrolytic solution. Particularly, in the 1.0 M (= mol L−1) LiNO3/G4 electrolyte under an O2 atmosphere, a Li2O protective layer is efficiently formed on the Li-metal electrode at a current density of 0.40 mA cm−2, and Li dendrite formation is suppressed. In the present study, we expanded the test conditions (current densities up to 2.0 mA cm−2 and temperatures of 10 to 50 °C) to clarify the dissolution/deposition behavior of the Li-metal NE. The effects of two electrolyte solutions, namely LiTFSI/G4 and LiNO3/G4, on the Li-metal NE were evaluated based on cyclical testing using Li|Li symmetric cells under an O2 atmosphere. The NEs were also examined by scanning electron microscopy and X-ray photoelectron spectroscopy. The results indicated that not only LiNO3 salt but also the supply of Li and nitrate ions at the Li electrode surface are critical factors in LAB performance. |
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Regarding the Li-metal negative electrode (NE), we have previously reported on the reversibility of the Li dissolution/deposition reaction by using Li|Li symmetric cells with a tetraglyme (G4)-based electrolytic solution. Particularly, in the 1.0 M (= mol L−1) LiNO3/G4 electrolyte under an O2 atmosphere, a Li2O protective layer is efficiently formed on the Li-metal electrode at a current density of 0.40 mA cm−2, and Li dendrite formation is suppressed. In the present study, we expanded the test conditions (current densities up to 2.0 mA cm−2 and temperatures of 10 to 50 °C) to clarify the dissolution/deposition behavior of the Li-metal NE. The effects of two electrolyte solutions, namely LiTFSI/G4 and LiNO3/G4, on the Li-metal NE were evaluated based on cyclical testing using Li|Li symmetric cells under an O2 atmosphere. The NEs were also examined by scanning electron microscopy and X-ray photoelectron spectroscopy. The results indicated that not only LiNO3 salt but also the supply of Li and nitrate ions at the Li electrode surface are critical factors in LAB performance.</description><identifier>ISSN: 1344-3542</identifier><identifier>EISSN: 2186-2451</identifier><identifier>DOI: 10.5796/electrochemistry.23-00142</identifier><language>eng ; jpn</language><publisher>Tokyo: The Electrochemical Society of Japan</publisher><subject>Atmosphere ; Batteries ; Current density ; Deposition ; Dissolution ; Electrodes ; Electrolytes ; Electrolytic cells ; Li Dissolution/deposition ; Li Metal Anode ; Li-air Battery (LAB) ; LiNO3 Electrolyte Solution ; Lithium oxides ; Metal air batteries ; Metals ; Photoelectron spectroscopy ; Photoelectrons ; Scanning electron microscopy ; X ray photoelectron spectroscopy</subject><ispartof>Electrochemistry, 2024/04/20, Vol.92(4), pp.047003-047003</ispartof><rights>The Author(s) 2023. Published by ECSJ.</rights><rights>2024. 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Regarding the Li-metal negative electrode (NE), we have previously reported on the reversibility of the Li dissolution/deposition reaction by using Li|Li symmetric cells with a tetraglyme (G4)-based electrolytic solution. Particularly, in the 1.0 M (= mol L−1) LiNO3/G4 electrolyte under an O2 atmosphere, a Li2O protective layer is efficiently formed on the Li-metal electrode at a current density of 0.40 mA cm−2, and Li dendrite formation is suppressed. In the present study, we expanded the test conditions (current densities up to 2.0 mA cm−2 and temperatures of 10 to 50 °C) to clarify the dissolution/deposition behavior of the Li-metal NE. The effects of two electrolyte solutions, namely LiTFSI/G4 and LiNO3/G4, on the Li-metal NE were evaluated based on cyclical testing using Li|Li symmetric cells under an O2 atmosphere. The NEs were also examined by scanning electron microscopy and X-ray photoelectron spectroscopy. The results indicated that not only LiNO3 salt but also the supply of Li and nitrate ions at the Li electrode surface are critical factors in LAB performance.</description><subject>Atmosphere</subject><subject>Batteries</subject><subject>Current density</subject><subject>Deposition</subject><subject>Dissolution</subject><subject>Electrodes</subject><subject>Electrolytes</subject><subject>Electrolytic cells</subject><subject>Li Dissolution/deposition</subject><subject>Li Metal Anode</subject><subject>Li-air Battery (LAB)</subject><subject>LiNO3 Electrolyte Solution</subject><subject>Lithium oxides</subject><subject>Metal air batteries</subject><subject>Metals</subject><subject>Photoelectron spectroscopy</subject><subject>Photoelectrons</subject><subject>Scanning electron microscopy</subject><subject>X ray photoelectron spectroscopy</subject><issn>1344-3542</issn><issn>2186-2451</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNplkd9u2yAUxlG1Sou6vgNTr93y5xiby7TNtkjRIq3tNcIGN0Su8YBMyhP0tYfrNhebhOBw9H0_PnEQ-krJdVlJcWN726bg2519cTGF4zXjBSEU2BlaMFqLgkFJP6EF5QAFL4F9Rpcx7knWECkkkwv0-rizeNV1GYR9hx8O49gf8S-d7HTdOLz2A9aDwcvB5Sqv3Lt3Mfr-kHLn5t6OPrqpxLd2p_84H7CbVD-3HK_mgP0x4x7eHRF3WbJxxdIFfKtTssHZ-AWdd7qP9vL9vEBP31aPdz-Kzfb7-m65KVogMhVSa0ErqIwBMFyIjshG6loa0pnSkBY0YQ1pJFS8FpY1ugVoOAPDaAm0rvgFWs9c4_VejcG96HBUXjv11vDhWemQXNtbVZlSCCOnD9VgJZWW1g1lkEkNKTvIrKuZNQb_-2BjUnt_CEOOrzgpcwRgXGSVnFVt8DEG251epURNY1T_jlExrt7GmL3b2buPST_bk_Mj4n9OyRRM2wfhpGx3Oig78L8AIbH6</recordid><startdate>20240420</startdate><enddate>20240420</enddate><creator>OZAWA, Fumisato</creator><creator>KOYAMA, Kazuki</creator><creator>IWASAKI, Daiki</creator><creator>AZUMA, Shota</creator><creator>NOMURA, Akihiro</creator><creator>SAITO, Morihiro</creator><general>The Electrochemical Society of Japan</general><general>Japan Science and Technology Agency</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QL</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>DOA</scope><orcidid>https://orcid.org/0009-0008-7214-0885</orcidid></search><sort><creationdate>20240420</creationdate><title>The Effect of Supply Rate of Li Ion and Anion on Li Dissolution/Deposition Behavior in LiNO3 Electrolyte Solutions for Li-Air Batteries</title><author>OZAWA, Fumisato ; 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Regarding the Li-metal negative electrode (NE), we have previously reported on the reversibility of the Li dissolution/deposition reaction by using Li|Li symmetric cells with a tetraglyme (G4)-based electrolytic solution. Particularly, in the 1.0 M (= mol L−1) LiNO3/G4 electrolyte under an O2 atmosphere, a Li2O protective layer is efficiently formed on the Li-metal electrode at a current density of 0.40 mA cm−2, and Li dendrite formation is suppressed. In the present study, we expanded the test conditions (current densities up to 2.0 mA cm−2 and temperatures of 10 to 50 °C) to clarify the dissolution/deposition behavior of the Li-metal NE. The effects of two electrolyte solutions, namely LiTFSI/G4 and LiNO3/G4, on the Li-metal NE were evaluated based on cyclical testing using Li|Li symmetric cells under an O2 atmosphere. The NEs were also examined by scanning electron microscopy and X-ray photoelectron spectroscopy. The results indicated that not only LiNO3 salt but also the supply of Li and nitrate ions at the Li electrode surface are critical factors in LAB performance.</abstract><cop>Tokyo</cop><pub>The Electrochemical Society of Japan</pub><doi>10.5796/electrochemistry.23-00142</doi><tpages>1</tpages><orcidid>https://orcid.org/0009-0008-7214-0885</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Atmosphere Batteries Current density Deposition Dissolution Electrodes Electrolytes Electrolytic cells Li Dissolution/deposition Li Metal Anode Li-air Battery (LAB) LiNO3 Electrolyte Solution Lithium oxides Metal air batteries Metals Photoelectron spectroscopy Photoelectrons Scanning electron microscopy X ray photoelectron spectroscopy |
title | The Effect of Supply Rate of Li Ion and Anion on Li Dissolution/Deposition Behavior in LiNO3 Electrolyte Solutions for Li-Air Batteries |
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