聚吡咯
材料科学
超级电容器
电极
电化学
储能
纳米技术
功率密度
电化学动力学
导电聚合物
化学工程
复合材料
电容
功率(物理)
聚合物
聚合
量子力学
物理
化学
物理化学
工程类
作者
Aifeng Liu,Jianxin Tang
标识
DOI:10.1016/j.ceramint.2020.01.103
摘要
Abstract For the creation of advanced electrochemical energy storage devices, a large challenge still remains in the designing and engineering of active electrodes with tailored nanoarchitectures and components that provide optimized electrochemical performances. In this study, CoMoO4@polypyrrole nano-heterostructures (NHs) are constructed by wrapping a polypyrrole (PPy) shell around the surface of CoMoO4 nanotubes (NTs) using a self-templated reaction and a subsequent in situ gas-phase polymerization reaction. CoMoO4 NTs possess a large amount of electroactive sites, short ion diffusion pathways, and provide sufficient buffering space. The PPy shell, on the other hand, is conductive, thereby allowing for efficient electron transport and fast charge transfer kinetics. By using their respective advantageous qualities for energy storage, along with the synergistic effect between the CoMoO4 NTs and PPy shell, the CoMoO4@PPy NHs electrode demonstrated improved specific capacitances of 1203 F g−1 at 2 A g−1 and 974 F g−1 at 20 A g−1, as well as 96% capacitance retention after 5000 cycles at 10 A g−1. Furthermore, asymmetric supercapacitor (ASC) fabricated using the CoMoO4@PPy//N-doped carbon NTs (N-CNTs) provided an energy density of 40.3 Wh kg−1 at a power density of 749 W kg−1. These results suggest the considerable potential of CoMoO4@PPy NHs for use in high-performance energy-storage devices.
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