{"title":"三维多孔亲锂基质实现无枝晶锂电沉积,制备稳定的锂金属阳极","authors":"Linghong Xu, Zhihao Yu, Junrong Zheng","doi":"10.1093/oxfmat/itab013","DOIUrl":null,"url":null,"abstract":"\n Lithium metal is a promising anode utilized in cutting-edge high-energy batteries owing to the low density, low electrochemical potential, and super high theoretical capacity. Unfortunately, continuous uncontrollable lithium dendrite growth and ‘dead’ lithium result in capacity decay, low coulombic efficiency, and short circuit, severely hindering the practical utilization of lithium anode. Herein, we propose a three-dimensional porous lithiophilic current collector for lithium storage. The conductive 3D structure constructed by carbon fiber (CF) can well accommodate the deposited lithium, eliminating volume change between the lithium depositing/stripping process. Moreover, the polydopamine (PDA) coating on the CF surface possesses a large number of polar groups, which can homogenize Li+ ions distribution and apply as the sites for lithium deposition, decreasing nucleation overpotential. As a result, under the 1 mA cm−2 current density, the PDA coated CF (PDA@CF) electrode exhibits high CE (∼98%) for 1000 cycles. Galvanostatic measurements demonstrate that the Li anode using PDA@CF achieves 1000 h cycling life under 1 mA cm−2 with a low overpotential (<15 mV). The LiFePO4 full cell shows enhanced rate performance and stable long-term cycling.","PeriodicalId":74385,"journal":{"name":"Oxford open materials science","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2021-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Dendrite-Free Lithium Electrodeposition Enabled by 3D Porous Lithiophilic Host toward Stable Lithium Metal Anodes\",\"authors\":\"Linghong Xu, Zhihao Yu, Junrong Zheng\",\"doi\":\"10.1093/oxfmat/itab013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n Lithium metal is a promising anode utilized in cutting-edge high-energy batteries owing to the low density, low electrochemical potential, and super high theoretical capacity. Unfortunately, continuous uncontrollable lithium dendrite growth and ‘dead’ lithium result in capacity decay, low coulombic efficiency, and short circuit, severely hindering the practical utilization of lithium anode. Herein, we propose a three-dimensional porous lithiophilic current collector for lithium storage. The conductive 3D structure constructed by carbon fiber (CF) can well accommodate the deposited lithium, eliminating volume change between the lithium depositing/stripping process. Moreover, the polydopamine (PDA) coating on the CF surface possesses a large number of polar groups, which can homogenize Li+ ions distribution and apply as the sites for lithium deposition, decreasing nucleation overpotential. As a result, under the 1 mA cm−2 current density, the PDA coated CF (PDA@CF) electrode exhibits high CE (∼98%) for 1000 cycles. Galvanostatic measurements demonstrate that the Li anode using PDA@CF achieves 1000 h cycling life under 1 mA cm−2 with a low overpotential (<15 mV). The LiFePO4 full cell shows enhanced rate performance and stable long-term cycling.\",\"PeriodicalId\":74385,\"journal\":{\"name\":\"Oxford open materials science\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2021-11-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oxford open materials science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/oxfmat/itab013\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oxford open materials science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/oxfmat/itab013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 1
摘要
金属锂由于其低密度、低电化学电势和超高理论容量,是一种很有前途的尖端高能电池阳极。不幸的是,持续不可控的锂枝晶生长和“死”锂导致容量衰减、库仑效率低和短路,严重阻碍了锂阳极的实际利用。在此,我们提出了一种用于锂存储的三维多孔亲锂集流体。由碳纤维(CF)构建的导电3D结构可以很好地容纳沉积的锂,消除了锂沉积/剥离过程之间的体积变化。此外,CF表面的聚多巴胺(PDA)涂层具有大量的极性基团,可以使Li+离子分布均匀,并作为锂沉积的位点,降低成核过电位。因此,在1 mA cm−2电流密度,PDA涂层CF(PDA@CF)电极在1000次循环中表现出高CE(~98%)。恒电流测量表明,使用PDA@CF达到1000 h循环寿命低于1 mA cm−2,具有低过电位(<15 mV)。LiFePO4全电池显示出增强的倍率性能和稳定的长期循环。
Dendrite-Free Lithium Electrodeposition Enabled by 3D Porous Lithiophilic Host toward Stable Lithium Metal Anodes
Lithium metal is a promising anode utilized in cutting-edge high-energy batteries owing to the low density, low electrochemical potential, and super high theoretical capacity. Unfortunately, continuous uncontrollable lithium dendrite growth and ‘dead’ lithium result in capacity decay, low coulombic efficiency, and short circuit, severely hindering the practical utilization of lithium anode. Herein, we propose a three-dimensional porous lithiophilic current collector for lithium storage. The conductive 3D structure constructed by carbon fiber (CF) can well accommodate the deposited lithium, eliminating volume change between the lithium depositing/stripping process. Moreover, the polydopamine (PDA) coating on the CF surface possesses a large number of polar groups, which can homogenize Li+ ions distribution and apply as the sites for lithium deposition, decreasing nucleation overpotential. As a result, under the 1 mA cm−2 current density, the PDA coated CF (PDA@CF) electrode exhibits high CE (∼98%) for 1000 cycles. Galvanostatic measurements demonstrate that the Li anode using PDA@CF achieves 1000 h cycling life under 1 mA cm−2 with a low overpotential (<15 mV). The LiFePO4 full cell shows enhanced rate performance and stable long-term cycling.