Hyeong-Seok Oh, Rae-Hyun Lee, Jong-Kyu Lee, Jung-Rag Yoon, Hyun-Kyung Kim and Seung-Hwan Lee
{"title":"提高循环耐久性并设计无树枝状突起的锂金属阳极","authors":"Hyeong-Seok Oh, Rae-Hyun Lee, Jong-Kyu Lee, Jung-Rag Yoon, Hyun-Kyung Kim and Seung-Hwan Lee","doi":"10.1039/D4MA00671B","DOIUrl":null,"url":null,"abstract":"<p >The development of Li metal batteries with increased lifespan and energy density is crucial for next-generation energy storage systems. To achieve this, it is necessary to control the growth of Li dendrites, which can lead to cycling performance issues and safety concerns. One approach to increase the energy density of large-scale Li metal-based batteries is to use thin Li metal anodes. However, fabricating thin Li metal anodes from natural oxide layers can be difficult. In this study, we used pure Li metal powder to fabricate thin Li metal anodes, which do not possess a natural oxide layer. This resulted in Li plating with a low overpotential on the unprotected Li metal surface. Our fabricated LiMP symmetric cell maintained stable cycling for over 170 hours at a current density of 1.0 mA cm<small><sup>−2</sup></small>, demonstrating superior performance compared to bare Li metal foil. Furthermore, we evaluated the performance of an all-solid-state battery (ASSB) using a polymer solid electrolyte and an oxide-based solid electrolyte in the fabricated LiMP symmetric cell. At 0.1 mA cm<small><sup>−2</sup></small>, the conventional Li symmetric cell experienced polarization after 200 hours, while the LiMP symmetric cell remained stable even after 600 hours. Taken together, these results provide new insights into the development of high-performance Li metal batteries.</p>","PeriodicalId":18242,"journal":{"name":"Materials Advances","volume":" 20","pages":" 8294-8303"},"PeriodicalIF":5.2000,"publicationDate":"2024-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ma/d4ma00671b?page=search","citationCount":"0","resultStr":"{\"title\":\"Attaining improved cycling durability and engineering a dendrite-free lithium metal anode\",\"authors\":\"Hyeong-Seok Oh, Rae-Hyun Lee, Jong-Kyu Lee, Jung-Rag Yoon, Hyun-Kyung Kim and Seung-Hwan Lee\",\"doi\":\"10.1039/D4MA00671B\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The development of Li metal batteries with increased lifespan and energy density is crucial for next-generation energy storage systems. To achieve this, it is necessary to control the growth of Li dendrites, which can lead to cycling performance issues and safety concerns. One approach to increase the energy density of large-scale Li metal-based batteries is to use thin Li metal anodes. However, fabricating thin Li metal anodes from natural oxide layers can be difficult. In this study, we used pure Li metal powder to fabricate thin Li metal anodes, which do not possess a natural oxide layer. This resulted in Li plating with a low overpotential on the unprotected Li metal surface. Our fabricated LiMP symmetric cell maintained stable cycling for over 170 hours at a current density of 1.0 mA cm<small><sup>−2</sup></small>, demonstrating superior performance compared to bare Li metal foil. Furthermore, we evaluated the performance of an all-solid-state battery (ASSB) using a polymer solid electrolyte and an oxide-based solid electrolyte in the fabricated LiMP symmetric cell. At 0.1 mA cm<small><sup>−2</sup></small>, the conventional Li symmetric cell experienced polarization after 200 hours, while the LiMP symmetric cell remained stable even after 600 hours. Taken together, these results provide new insights into the development of high-performance Li metal batteries.</p>\",\"PeriodicalId\":18242,\"journal\":{\"name\":\"Materials Advances\",\"volume\":\" 20\",\"pages\":\" 8294-8303\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2024-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ma/d4ma00671b?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Materials Advances\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ma/d4ma00671b\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Advances","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ma/d4ma00671b","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
开发具有更长使用寿命和更高能量密度的锂金属电池对下一代储能系统至关重要。要实现这一目标,必须控制锂枝晶的生长,否则会导致循环性能问题和安全隐患。提高大规模金属锂电池能量密度的一种方法是使用薄金属锂阳极。然而,利用天然氧化物层制造薄金属锂阳极可能很困难。在本研究中,我们使用纯锂金属粉末来制造薄型锂金属阳极,这种阳极不具有天然氧化层。这使得锂镀层在未受保护的锂金属表面具有较低的过电位。我们制备的 LiMP 对称电池在 1.0 mA cm-2 的电流密度下可稳定循环 170 多个小时,与裸锂金属箔相比性能更优。此外,我们还评估了全固态电池(ASSB)的性能,在制备的锂金属氧化物对称电池中使用了聚合物固态电解质和氧化物固态电解质。在 0.1 mA cm-2 的条件下,传统的对称锂电池在 200 小时后出现极化,而对称锂聚合物电池即使在 600 小时后仍能保持稳定。综上所述,这些结果为开发高性能锂金属电池提供了新的思路。
Attaining improved cycling durability and engineering a dendrite-free lithium metal anode
The development of Li metal batteries with increased lifespan and energy density is crucial for next-generation energy storage systems. To achieve this, it is necessary to control the growth of Li dendrites, which can lead to cycling performance issues and safety concerns. One approach to increase the energy density of large-scale Li metal-based batteries is to use thin Li metal anodes. However, fabricating thin Li metal anodes from natural oxide layers can be difficult. In this study, we used pure Li metal powder to fabricate thin Li metal anodes, which do not possess a natural oxide layer. This resulted in Li plating with a low overpotential on the unprotected Li metal surface. Our fabricated LiMP symmetric cell maintained stable cycling for over 170 hours at a current density of 1.0 mA cm−2, demonstrating superior performance compared to bare Li metal foil. Furthermore, we evaluated the performance of an all-solid-state battery (ASSB) using a polymer solid electrolyte and an oxide-based solid electrolyte in the fabricated LiMP symmetric cell. At 0.1 mA cm−2, the conventional Li symmetric cell experienced polarization after 200 hours, while the LiMP symmetric cell remained stable even after 600 hours. Taken together, these results provide new insights into the development of high-performance Li metal batteries.