{"title":"利用金涂层隔板引导锂的生长方向,改进锂金属负极","authors":"Zhouting Sun, Qihang Zhang, Zhenyu Wang, Yifei Chen, Kaiming Wang, Fei Shen, Juchen Guo, Xiaogang Han","doi":"10.20517/energymater.2024.03","DOIUrl":null,"url":null,"abstract":"Lithium metal is the most promising anode for next-generation batteries due to its highest theoretical capacity and lowest electrochemical potential. However, its dendritic growth hinders its practical use due to the consequent poor reversibility, potential short-circuit, and safety concerns. Suppressing lithium dendrite is difficult since dendritic growth is thermodynamically and kinetically favorable. Herein, we guide lithium to uniformly deposit along the opposite direction to normal by a nanolayer Au coating on a commercial polypropylene separator. It prevents lithium dendrites from piercing the separator, instead of inhibiting dendrites growth only. Au is lithiophilic, and lithium is calculated to be more attracted to Au and is confirmed to uniformly deposit on Au at the separator side rather than on the current collector side. Furthermore, Au also regulates the morphology of deposited lithium from a mossy state to a bulky state. In this work, the symmetric cell with the designed structure achieves excellent electrochemical performances of a long-life cycle over 2,000 h at 1 C for 1 mA h cm-2. Pairing with LiFePO4 cathode as a full cell, lithium metal anode with Au-modified polypropylene separator exhibits extraordinary performance with a high Coulombic efficiency of 99.23% over 800 cycles at 1 C.","PeriodicalId":516139,"journal":{"name":"Energy Materials","volume":"35 5","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Guiding lithium growth direction by Au coated separator for improving lithium metal anode\",\"authors\":\"Zhouting Sun, Qihang Zhang, Zhenyu Wang, Yifei Chen, Kaiming Wang, Fei Shen, Juchen Guo, Xiaogang Han\",\"doi\":\"10.20517/energymater.2024.03\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Lithium metal is the most promising anode for next-generation batteries due to its highest theoretical capacity and lowest electrochemical potential. However, its dendritic growth hinders its practical use due to the consequent poor reversibility, potential short-circuit, and safety concerns. Suppressing lithium dendrite is difficult since dendritic growth is thermodynamically and kinetically favorable. Herein, we guide lithium to uniformly deposit along the opposite direction to normal by a nanolayer Au coating on a commercial polypropylene separator. It prevents lithium dendrites from piercing the separator, instead of inhibiting dendrites growth only. Au is lithiophilic, and lithium is calculated to be more attracted to Au and is confirmed to uniformly deposit on Au at the separator side rather than on the current collector side. Furthermore, Au also regulates the morphology of deposited lithium from a mossy state to a bulky state. In this work, the symmetric cell with the designed structure achieves excellent electrochemical performances of a long-life cycle over 2,000 h at 1 C for 1 mA h cm-2. Pairing with LiFePO4 cathode as a full cell, lithium metal anode with Au-modified polypropylene separator exhibits extraordinary performance with a high Coulombic efficiency of 99.23% over 800 cycles at 1 C.\",\"PeriodicalId\":516139,\"journal\":{\"name\":\"Energy Materials\",\"volume\":\"35 5\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy Materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20517/energymater.2024.03\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20517/energymater.2024.03","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
锂金属具有最高的理论容量和最低的电化学势,是下一代电池最有前途的阳极。然而,由于树枝状生长带来的可逆性差、潜在短路和安全问题,阻碍了其实际应用。由于树枝状生长在热力学和动力学上都是有利的,因此抑制锂树枝状生长十分困难。在这里,我们通过在商用聚丙烯隔膜上镀一层纳米金,引导锂沿着与正常方向相反的方向均匀沉积。它能防止锂枝晶刺穿隔膜,而不是仅仅抑制枝晶的生长。金具有亲锂性,根据计算,锂对金的吸引力更大,并证实锂会均匀地沉积在隔板一侧的金上,而不是集流器一侧。此外,金还能调节沉积锂的形态,使其从苔藓状变为膨大状。在这项工作中,采用所设计结构的对称电池实现了出色的电化学性能,在 1 C 温度、1 mA h cm-2 条件下可实现超过 2,000 小时的长寿命循环。将锂金属阳极与磷酸铁锂阴极配对作为全电池,再加上金改性聚丙烯隔膜,在 1 C 条件下循环 800 次,库仑效率高达 99.23%,表现出非凡的性能。
Guiding lithium growth direction by Au coated separator for improving lithium metal anode
Lithium metal is the most promising anode for next-generation batteries due to its highest theoretical capacity and lowest electrochemical potential. However, its dendritic growth hinders its practical use due to the consequent poor reversibility, potential short-circuit, and safety concerns. Suppressing lithium dendrite is difficult since dendritic growth is thermodynamically and kinetically favorable. Herein, we guide lithium to uniformly deposit along the opposite direction to normal by a nanolayer Au coating on a commercial polypropylene separator. It prevents lithium dendrites from piercing the separator, instead of inhibiting dendrites growth only. Au is lithiophilic, and lithium is calculated to be more attracted to Au and is confirmed to uniformly deposit on Au at the separator side rather than on the current collector side. Furthermore, Au also regulates the morphology of deposited lithium from a mossy state to a bulky state. In this work, the symmetric cell with the designed structure achieves excellent electrochemical performances of a long-life cycle over 2,000 h at 1 C for 1 mA h cm-2. Pairing with LiFePO4 cathode as a full cell, lithium metal anode with Au-modified polypropylene separator exhibits extraordinary performance with a high Coulombic efficiency of 99.23% over 800 cycles at 1 C.