Jiaqi Zhu , Han Su , Juner Kuang , Yu Zhong , Xiuli Wang , Jiangping Tu
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Assembling electrode units collaboratively establishes the ion-electron percolating network within the LGMF, fully activating the entire anode. The optimized LGMF anodes extend the longevity of carbonate-based quasi-solid-state symmetric cells to 2400 h at 0.2 mA cm<sup>−2</sup>/0.2 mAh cm<sup>−2</sup>, even under limited lithium conditions. LiFePO<sub>4</sub> full cells utilizing LGMF anodes exhibit steady galvanostatic cycling over 400 cycles, attaining a notable capacity retention of 95.5 % at 0.5 C. Meanwhile, the LGMF||LiNi<sub>0.83</sub>Co<sub>0.12</sub>Mn<sub>0.05</sub>O<sub>2</sub> cells demonstrate enhanced rate capability and prolonged electrochemical lifespan. 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引用次数: 0
摘要
利用薄锂阳极是实现高能量密度固态锂金属电池的关键。然而,锂枝晶不可避免的形成,以及界面副反应引起的锂耗竭,给薄锂阳极的实际实施带来了很大的挑战。为了解决这个问题,我们提出了一种集总Li-Gr@MgF2 (LGMF)阳极,由锂化mgf2涂层石墨组成,通过自下而上的集成精确地重建了贫锂金属阳极。优化后的LiC6-LiMg/LiF电极单元具有亲锂性Li-Mg合金和高界面能LiF界面修饰,可调节锂离子通量,有效抑制枝晶生长。组装电极单元协同建立LGMF内的离子-电子渗透网络,充分激活整个阳极。优化后的LGMF阳极在0.2 mA cm - 2/0.2 mAh cm - 2条件下,即使在有限的锂条件下,碳化物基准固态对称电池的寿命也可延长至2400小时。使用LGMF阳极的LiFePO4全电池在0.5 c下具有稳定的恒流循环超过400次,达到95.5%的显着容量保持率。同时,LGMF||LiNi0.83Co0.12Mn0.05O2电池具有增强的倍率能力和延长的电化学寿命。该策略为实现高能量密度sslmb的贫锂金属阳极工程提供了实用的见解。
A lean-lithium metal anode based on Gr@MgF2 for solid-state batteries
Utilizing thin Li anodes is the key to realizing high-energy-density solid-state lithium metal batteries (SSLMBs). However, the practical implementation of thin Li anodes is significantly challenged by the inevitable formation of lithium dendrites, as well as the lithium depletion caused by interfacial side reactions. To address this, we propose a lumped Li-Gr@MgF2 (LGMF) anode comprised of lithiated MgF2-coated graphite, which precisely reconstructs the lean-lithium metal anode through bottom-up integration. Finely optimized electrode units of LiC6-LiMg/LiF possess lithiophilic Li-Mg alloy and high-interface-energy LiF interfacial modification, which regulate the lithium-ion flux and effectively suppress dendrite growth. Assembling electrode units collaboratively establishes the ion-electron percolating network within the LGMF, fully activating the entire anode. The optimized LGMF anodes extend the longevity of carbonate-based quasi-solid-state symmetric cells to 2400 h at 0.2 mA cm−2/0.2 mAh cm−2, even under limited lithium conditions. LiFePO4 full cells utilizing LGMF anodes exhibit steady galvanostatic cycling over 400 cycles, attaining a notable capacity retention of 95.5 % at 0.5 C. Meanwhile, the LGMF||LiNi0.83Co0.12Mn0.05O2 cells demonstrate enhanced rate capability and prolonged electrochemical lifespan. This strategy offers practical insight for lean-lithium metal anode engineering toward high-energy-density SSLMBs.
期刊介绍:
Nano Energy is a multidisciplinary, rapid-publication forum of original peer-reviewed contributions on the science and engineering of nanomaterials and nanodevices used in all forms of energy harvesting, conversion, storage, utilization and policy. Through its mixture of articles, reviews, communications, research news, and information on key developments, Nano Energy provides a comprehensive coverage of this exciting and dynamic field which joins nanoscience and nanotechnology with energy science. The journal is relevant to all those who are interested in nanomaterials solutions to the energy problem.
Nano Energy publishes original experimental and theoretical research on all aspects of energy-related research which utilizes nanomaterials and nanotechnology. Manuscripts of four types are considered: review articles which inform readers of the latest research and advances in energy science; rapid communications which feature exciting research breakthroughs in the field; full-length articles which report comprehensive research developments; and news and opinions which comment on topical issues or express views on the developments in related fields.