电解质
硫化物
锂(药物)
超晶格
材料科学
阴极
导电体
固态
快离子导体
电池(电)
化学工程
纳米技术
化学
电极
光电子学
冶金
复合材料
物理化学
工程类
物理
医学
功率(物理)
量子力学
内分泌学
作者
Ruru Meng,Jinghua Wu,Mengting Zhu,Wenrui Xie,Mengli Yang,Fuli Tian,Xiayin Yao
标识
DOI:10.1016/j.cej.2024.152540
摘要
Sulfide electrolytes play a crucial role in the pursuit of high-performance all-solid-state lithium batteries (ASSLBs). However, most sulfide electrolytes have intrinsic narrow electrochemical stability windows, and decomposition reactions are thermodynamically favorable, especially contact with conductive additive. These ongoing side reactions accelerate sulfide electrolytes degradation, posing a significant threat to the cycling stability of ASSLBs. Herein, we propose an effective approach to address this challenge by designing a MoS2-C superlattice structure. This architecture, characterized by a layer-by-layer inter-stacking of MoS2 nanosheets and carbon layers, endows it with excellent electronic conductivity and enhanced lithium diffusion kinetics. Leveraging this superlattice, ASSLBs incorporating MoS2-C superlattice as the cathode without conductive additive exhibit a substantial improvement in electrochemical performance, ultimately achieving a conductive additive-free ASSLBs. Remarkably, the conductive additive-free ASSLBs based on the MoS2-C superlattice demonstrates outstanding stability, enduring 300 cycles with a capacity retention of 96.8 % at a 1 C rate. This enhancement can be attributed to the improved charge transfer kinetics of MoS2-C superlattice and the effective suppression of side reactions between the sulfide electrolyte and conductive additive. Our study presents a promising design strategy to achieve high-rate performance and tackle long-term challenges in the application of sulfide electrolytes-based ASSLBs.
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