Linker length-dependent lithium storage of pyrene-4,5,9,10-tetraone-based conjugated organic polymer cathodes

被引:0
作者
Li, Yuke [1 ]
Xia, Zhelin [3 ]
Zhang, Yuemiao [2 ]
Xue, Xinxian [1 ]
Chen, Lei [1 ]
Wu, Di [1 ]
Wang, Yujing [1 ]
Chen, Xianlang [1 ]
Ren, Shi-Bin [1 ,3 ]
Han, De-Man [1 ,3 ]
Xu, Yubin [3 ]
机构
[1] Taizhou Univ, Sch Pharmaceut & Chem Engn, Taizhou 318000, Peoples R China
[2] Taizhou Vocat Coll Sci & Technol, Dept Agr & Biotechnol, Taizhou 318020, Peoples R China
[3] Taizhou Univ, Taizhou Univ Hosp, Taizhou Cent Hosp, Dept Clin Lab, Taizhou 318000, Peoples R China
基金
中国博士后科学基金;
关键词
Conjugated organic polymers; Linker length; Lithium-ion batteries; Cathodes; Stability; FAST-CHARGE; PERFORMANCE; BATTERIES; CAPACITY;
D O I
10.1016/j.electacta.2024.145257
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Conjugated organic polymers (COPs) have been emerged as a class of cathode materials for lithium-ion batteries (LIBs) because of the rigid structural units and tunable properties. Nonetheless, their applications are still limited due to the poor conductivity and low cycling life. Herein, we design a series of pyrene-4,5,9,10-tetraone-based COPs (P(PTODB)-1, P(PTODB)-2, P(PTODB)-3), containing different number of benzene rings as linking units. Consequently, prolonging the linker lengths could effectively improve structural stability and extend pi-conjugation, leading to the enhanced charge-storage capability. When tested as cathode materials for LIBs, the P (PTODB)-2 electrode delivers a better electrochemical performance with high capacity of 203 mA h g-1 after 100 cycles at 0.1 A g-1 (coulombic efficiency almost 100%) and excellent rate performance (150 mA h g-1 at 5 A g-1). In addition, the Li+ storage mechanism was carried out by ex situ Fourier transform infrared (FT-IR) and X-ray photoelectron spectroscopy (XPS) analysis. Eventually, our study brings forward the appropriately extended linker lengths to fabricate COP cathodes with high electrochemical properties.
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页数:7
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