In Situ Interfacial Tuning To Obtain High-Performance Nickel-Rich Cathodes in Lithium Metal Batteries

材料科学 电解质 电化学 乙醚 锂(药物) 溶解 阴极 无机化学 化学工程 过渡金属 电极 阳极 有机化学 冶金 化学 催化作用 医学 物理化学 工程类 内分泌学
作者
Hyunsoo Ma,Daeyeon Hwang,Young Jun Ahn,Min‐Young Lee,Saehun Kim,Yong‐Won Lee,Sang‐Min Lee,Sang Kyu Kwak,Nam‐Soon Choi
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:12 (26): 29365-29375 被引量:30
标识
DOI:10.1021/acsami.0c06830
摘要

Nickel-rich layered oxides are currently considered the most practical candidates for realizing high-energy-density lithium metal batteries (LMBs) because of their relatively high capacities. However, undesired nickel-rich cathode-electrolyte interactions hinder their applicability. Here, we report a satisfactory combination of an antioxidant fluorinated ether solvent and an ionic additive that can form a stable, robust interfacial structure on the nickel-rich cathode in ether-based electrolytes. The fluorinated ether 1,1,2,2-tetrafluoroethyl-1H,1H,5H-octafluoropentyl ether (TFOFE) introduced as a cosolvent into ether-based electrolytes stabilizes the electrolytes against oxidation at the LiNi0.8Mn0.1Co0.1O2 (NCM811) cathode while simultaneously preserving the electrochemical performance of the Li metal anode. Lithium difluoro(bisoxalato)phosphate (LiDFBP) forms a uniform cathode-electrolyte interphase that limits the generation of microcracks inside secondary particles and undesired dissolution of transition metal ions such as nickel, cobalt, and manganese from the cathode into the electrolyte. Using TFOFE and LiDFBP in ether-based electrolytes provides an excellent capacity retention of 94.5% in a Li|NCM811 cell after 100 cycles and enables the delivery of significantly increased capacity at high charge and discharge rates by manipulating the interfaces of both electrodes. This research provides insights into advancing electrolyte technologies to resolve the interfacial instability of nickel-rich cathodes in LMBs.
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