Molecule and Microstructure Modulations of Cyano-Containing Electrodes for High-Performance Fully Organic Batteries

被引:2
|
作者
Wang, Yonglin [1 ]
Zhu, Yunhai [1 ]
Chen, Zixuan [1 ]
Yang, Xu [2 ]
Zhang, Rongyu [2 ]
Wang, Hengguo [3 ,4 ]
Yang, Yingkui [1 ]
机构
[1] Wuhan Text Univ, State Key Lab New Text Mat & Adv Proc Technol, Wuhan 430200, Peoples R China
[2] Shenyang Aerosp Univ, Coll Sci, Shenyang 110135, Peoples R China
[3] Northeast Normal Univ, Key Lab Polyoxometalate & Reticular Mat Chem, Minist Educ, Changchun 130024, Peoples R China
[4] Northeast Normal Univ, Fac Chem, Changchun 130024, Peoples R China
基金
中国国家自然科学基金;
关键词
electronic modulation; molecular design; core-sheath heterostructures; cyanopolymer; fully organic battery; LITHIUM-ION; CARBON NANOTUBES; HIGH-ENERGY; FRAMEWORKS; ELECTROPHILICITY; NUCLEOPHILICITY; RICH;
D O I
10.1002/anie.202401253
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyano-containing electrodes usually promise high theoretical potentials while suffering from uncontrollable self-dissolution and sluggish reaction kinetics. Herein, to remedy their limitations, an unprecedented core-shell heterostructured electrode of carbon nanotubes encapsulated in poly(1,4-dicyanoperfluorobenzene sulfide) (CNT@PFDCB) is rationally crafted via molecule and microstructure modulations. Specifically, the linkage of sulfide bridges of PFDCB prevents the active cyano groups from dissolving, resulting in a robust structure. The fluorinations modulate the electronic configurations in frontier orbitals, allowing higher electrical conductivity and elevated output voltage. Combined with the core-shell architecture to unlock the sluggish diffusion kinetics for both electrons and guest ions, the CNT@PFDCB exhibits an impressive capacity (203.5 mAh g-1), remarkable rate ability (127.6 mAh g-1 at 3.0 A g-1), and exceptional cycling stability (retaining 81.1 % capacity after 3000 cycles at 1.0 A g-1). Additionally, the Li-storage mechanisms regarding PFDCB are thoroughly revealed by in situ attenuated total reflection infrared spectroscopy, in situ Raman spectroscopy, and theoretical simulations, which involve the coordination interaction between Li ions and cyano groups and the electron delocalization along the conjugated skeleton. More importantly, a practical fully organic cell based on the CNT@PFDCB is well-validated that demonstrates a tremendous potential of cyanopolymer as the cathode to replace its inorganic counterparts. Molecule and microstructure modulations of cyano-containing electrodes craft a groundbreaking CNT@PFDCB with core-shell heterostructure, which breaks through the limitations of cyano-containing electrodes including inevitable self-dissolution and sluggish reaction kinetics. As a result, the novel CNT@PFDCB achieves high capacity, elevated voltage, superior rate ability, and exceptional cycling stability, standing out among the reported organic cathodes. image
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页数:10
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