共聚物
复合材料
材料科学
锂(药物)
涂层
盐(化学)
阴极
电极
块(置换群论)
化学工程
高分子化学
化学
聚合物
有机化学
医学
几何学
数学
物理化学
工程类
内分泌学
作者
Qiaoyun Wu,Zhuijun Xu,Ying Yu,Meilan Peng,Jie Gao,Lei Nie,Ya‐Jun Cheng,Peter Müller‐Buschbaum,Yonggao Xia
出处
期刊:Langmuir
[American Chemical Society]
日期:2024-07-12
卷期号:40 (29): 14863-14871
被引量:9
标识
DOI:10.1021/acs.langmuir.4c00776
摘要
Nickel-rich layered oxide cathodes, such as LiNi0.5Co0.2Mn0.3O2 (NCM523), are prevalent in high-power batteries owing to their high energy density. However, these cathodes suffer from undesirable side reactions occurring at the cathode/liquid electrolyte interface, leading to inferior interface stability and poor cycle life. To address these issues, herein, an amphiphilic diblock copolymer poly(dimethylsiloxane)-block-poly(acrylic acid) (PDMS-b-PAA) along with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) is utilized for modifying the electrode surface. This modification causes a thin and stable cathode–electrolyte interface (CEI) on the surface of NCM523 particles, as evidenced by XPS, TEM, and EIS analysis. The introduction of this modified interface successfully suppresses the capacity fading of NCM523. After 200 cycles at a rate of 1.0 C, the capacity of the modified NCM523 cathode is 108.7 mAh g–1, with a capacity retention of 82.8%, while the control samples without the polymer modification display a capacity retention of 72.7%. These results outline the distinct advantage of electrode surface modification with diblock copolymers/LiTFSI for the stabilization of Ni-rich layered oxide cathodes.
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