材料科学
碳纳米管
阴极
共轭体系
钠
化学工程
储能
聚合
聚合物
电极
复合材料
电化学
纳米技术
化学
功率(物理)
物理
物理化学
量子力学
工程类
冶金
作者
Ruijuan Shi,Luojia Liu,Yong Lü,Yixin Li,Shibing Zheng,Zhenhua Yan,Kai Zhang,Jun Chen
标识
DOI:10.1002/aenm.202002917
摘要
Abstract Sodium batteries have attracted much attention in recent years because of their comprehensive electrochemical performance, high abundance, and low cost of sodium resources. However, the unsatisying energy density and poor cycling stability of current sodium batteries restrict their large‐scale applications. Here an in situ polymerization method to construct π‐conjugated poly(pyrene‐4,5,9,10‐tetraone)/carbon nanotubes (PPTO–CNTs) composites as cathode materials for sodium batteries is used. It is found that the π–π interaction between PPTO and CNTs in PPTO–CNTs composites overcomes the repulsion between each PPTO unit, leading to a flat configuration of PPTO and enhancing the electronic conductivity and active sites accessibility of PPTO–CNTs composites. Thus, PPTO–CNTs electrodes display a high discharge capacity of 360.2 mAh g −1 , long cycling stability (a capacity retention of 95.1% after 1300 cycles), and high rate capability (194.5 mAh g −1 at 10.0 A g −1 ). Moreover, a pouch‐type Na//PPTO–CNTs cell with an energy density of ≈ 204.0 Wh kg −1 PPTO+Na is fabricated, exhibiting a capacity retention of 91.2% after 100 cycles. In addition, the combination of experiments and theoretical calculations demonstrates the four‐sodium‐ion redox chemistry mechanism of each PPTO molecule unit. This work should promote the practical application of conjugated polymers in high‐performance sodium batteries.
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