Amphiphilic surfactant-assisted cathode-electrolyte interphases for prolonged cycling performance in Ni-rich NCMA cathode materials of lithium-ion batteries

被引:0
|
作者
Kim, Soon Young [1 ,2 ]
Lee, Subin [1 ,2 ]
Yoon, Sae Chan [1 ,2 ]
Yim, Taeeun [1 ,2 ]
机构
[1] Incheon Natl Univ, Adv Batteries Lab, Dept Chem, 119 Acad Ro, Incheon 22012, South Korea
[2] Incheon Natl Univ, Res Inst Basic Sci, Coll Nat Sci, 119 Acad Ro, Incheon 22012, South Korea
基金
新加坡国家研究基金会;
关键词
Lithium-ion battery; Nickel-rich layered oxide cathode; Coating; 3-(N; N-dimethylpalmitylammonio); propanesulfonate; Surfactant; Electrochemical performance; ELECTROCHEMICAL PERFORMANCE; IMPACT;
D O I
10.1016/j.jpowsour.2025.236447
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
The nickel-rich LiNixCoyMnzAl1-x-y-zO2 (x + y + z = 1, NCMA) layered cathode has recently attracted attention as a promising cathode material; however, its lifespan is shortened upon cycling due to its poor interfacial stability. Our attempts to prolong its lifespan included modifying the surface of the NCMA cathode using an amphipathic coating precursor, 3-(N,N-dimethylpalmitylammonio) propanesulfonate (PAPS). Favorable chemical interactions between the hydrophilic PAPS precursor and hydrophilic surface of the NCMA cathode allow the sulfonate functional groups of the precursor to attach to the NCMA cathode surface. The subsequent heating process results in the formation of uniformly distributed cathode-electrolyte interphase (CEI) layers, which effectively suppress electrolyte decomposition. Consequently, the capacity retention of the PAPS-modified NCMA cathode improves at both room temperature (92.7%) and elevated temperatures (86.4%) compared with that of the pristine NCMA cathode (58.5% and 28.8%, respectively). Additional systematic analyses indicate that the PAPS-derived CEI layers improve the interfacial stability of the NCMA cathodes.
引用
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页数:10
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