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Electrochemical polymerization of pyrene derivatives on functionalized carbon nanotubes for pseudocapacitive electrodes

机译:pseudo电极在功能化碳纳米管上derivatives衍生物的电化学聚合。

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摘要

Electrochemical energy-storage devices have the potential to be clean and efficient, but their current cost and performance limit their use in numerous transportation and stationary applications. Many organic molecules are abundant, economical and electrochemically active; if selected correctly and rationally designed, these organic molecules offer a promising route to expand the applications of these energy-storage devices. In this study, polycyclic aromatic hydrocarbons are introduced within a functionalized few-walled carbon nanotube matrix to develop high-energy, high-power positive electrodes for pseudocapacitor applications. The reduction potential and capacity of various polycyclic aromatic hydrocarbons are correlated with their interaction with the functionalized few-walled carbon nanotube matrix, chemical configuration and electronic structure. These findings provide rational design criteria for nanostructured organic electrodes. When combined with lithium negative electrodes, these nanostructured organic electrodes exhibit energy densities of ∼350 Wh kg−1electrode at power densities of ∼10 kW kg−1electrode for over 10,000 cycles.
机译:电化学储能设备具有清洁和高效的潜力,但是其当前的成本和性能限制了其在众多运输和固定应用中的使用。许多有机分子丰富,经济且具有电化学活性。如果正确选择和合理设计,这些有机分子将为扩展这些储能设备的应用提供一条有希望的途径。在这项研究中,将多环芳烃引入功能化的短壁碳纳米管基质中,以开发用于伪电容器应用的高能量,高功率正极。各种多环芳烃的还原电位和容量与其与官能化的短壁碳纳米管基质的相互作用,化学构型和电子结构相关。这些发现为纳米结构的有机电极提供了合理的设计标准。当与锂负极组合使用时,这些纳米结构的有机电极的能量密度为〜10 kW kg -1 电极,能量密度为350 Wh kg -1 电极超过10,000周期。

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