电解质
材料科学
阳极
扩散
锂(药物)
溶剂化
电子顺磁共振
金属锂
离子键合
金属
热扩散率
化学工程
枝晶(数学)
沉积(地质)
无机化学
离子电导率
工作(物理)
电池(电)
离子
分析化学(期刊)
化学物理
核磁共振
自行车
共振(粒子物理)
作者
Y. H. Fan,Jinlong Sun,Sen Ma,Mengdi Chen,Xiaobing Lou,Bingwen Hu
标识
DOI:10.1021/acs.jpclett.5c03697
摘要
Lithium metal batteries face significant challenges in achieving stable high-rate cycling due to uncontrolled Li dendrite growth and poor interfacial stability. This study proposes a localized relative-high concentration electrolyte to enable high-rate operation without sacrificing ionic transport. By comparing three localized high-concentration electrolytes (3M|1M denoting 3M LiFSI in DME and 1 M LiFSI in DME&TTE, 5M|2M and 8M|3M) with diffusion NMR, we demonstrate that the 5M|2M system achieves an optimal balance between Li+ diffusivity and anion-derived solvation structure, facilitating a robust inorganic-rich SEI. Employing electron paramagnetic resonance imaging (EPRI) with ultrahigh spatial resolution, we visualize the uniform Li deposition and minimal dead Li formation in the 5M|2M electrolyte due to balanced LiF content and F-S content in SEI. This work provides new insights into electrolyte engineering for fast-charging lithium metal batteries, highlighting the critical role of concentration-mediated SEI formation in stabilizing Li anode interfaces under high-rate conditions.
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