In-situ coating strategy to synthesize ultra-soft sulfide solid-state electrolytes for dendrite-free lithium metal batteries

被引:6
|
作者
Yuan, Haoyang [1 ]
Lin, Wenjun [2 ]
Tian, Changhao [1 ]
Huang, Tao [2 ]
Yu, Aishui [1 ,2 ]
机构
[1] Fudan Univ, Inst New Energy, Shanghai Key Lab Mol Catalysis & Innovat Mat, Dept Chem,Collaborat Innovat Ctr Chem Energy Mat, Shanghai 200438, Peoples R China
[2] Fudan Univ, Lab Adv Mat, Shanghai 200438, Peoples R China
关键词
All-solid-state electrolytes; Lithium metal anode; In-situ polymerization; Polymer coating; Interfacial evolution;
D O I
10.1016/j.nanoen.2024.109835
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
High energy density lithium metal batteries play a crucial role in future energy storage. High ionic conductivity argyrodite-type Li5.5PS4.5Cl1.5 is a promising candidate for future lithium metal all-solid-state batteries. However, under cold pressing conditions, the combination of high electronic conductivity and high porosity significantly accelerates the growth of lithium dendrites, resulting in low capacity and a short lifespan. In this study, we combined a simple wet ball milling and in-situ polymerization process to fabricate a polyvinylene carbonatecoated sulfide composite solid electrolyte. The ultra-soft particle, when cold-pressed without binders, completed a tightly packed and void-free internal structure. This electrolyte, combined with a stable LiF-rich interface layer on lithium metal, held a higher critical current density of 2.0 mA cm- 2 than 0.65 mA cm- 2 of uncoated argyrodite and a 2000-hour stable cycle at 0.5 mA cm-2 in lithium symmetric cells. The unique coating structure also mitigated the chemomechanical failure between electrolyte and electrode, preventing the rapid increase of interface impedance and achieving a high initial capacity of 173.5 mAh g-1 without a short circuit for 300 cycles in LiNi0.6Co0.2Mn0.2O2//Li cells.
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页数:10
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