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一种简便的一步法制备聚吡咯纳米线/碳纤维混合电极,用于柔性高性能固态超级电容器。

A facile one-step approach for the fabrication of polypyrrole nanowire/carbon fiber hybrid electrodes for flexible high performance solid-state supercapacitors.

机构信息

National Engineering Lab for Textile Fiber Materials & Processing Technology (Zhejiang), Faculty of Materials and Textiles, Zhejiang Sci-Tech University, Hangzhou 310018, People's Republic of China.

出版信息

Nanotechnology. 2017 Oct 27;28(43):435204. doi: 10.1088/1361-6528/aa84cb. Epub 2017 Aug 8.

DOI:10.1088/1361-6528/aa84cb
PMID:28786401
Abstract

Wearable electronics are in high demand, requiring that all the components are flexible. Here we report a facile approach for the fabrication of flexible polypyrrole nanowire (NPPy)/carbon fiber (CF) hybrid electrodes with high electrochemical activity using a low-cost, one-step electrodeposition method. The structure of the NPPy/CF electrodes can be easily controlled by the applied electrical potential and electrodeposition time. Our NPPy/CF-based electrodes showed high flexibility, conductivity, and stability, making them ideal for flexible all-solid-state fiber supercapacitors. The resulting NPPy/CF-based supercapacitors provided a high specific capacitance of 148.4 F g at 0.128 A g, which is much higher than for supercapacitors based on polypyrrole film/CF (38.3 F g) and pure CF (0.6 F g) under the same conditions. The NPPy/CF-based supercapacitors also showed high bending and cycling stability, retaining 84% of the initial capacitance after 500 bending cycles, and 91% of the initial capacitance after 5000 charge/discharge cycles.

摘要

可穿戴电子产品需求旺盛,要求所有组件都具有柔韧性。在这里,我们报告了一种使用低成本、一步电沉积方法制造具有高电化学活性的柔性聚吡咯纳米线(NPPy)/碳纤维(CF)杂化电极的简便方法。通过施加的电势和电沉积时间可以轻松控制 NPPy/CF 电极的结构。我们的 NPPy/CF 基电极具有高柔韧性、导电性和稳定性,非常适合用于柔性全固态纤维超级电容器。基于 NPPy/CF 的超级电容器的比电容高达 148.4 F g,在 0.128 A g 下,比基于聚吡咯膜/CF(38.3 F g)和纯 CF(0.6 F g)的超级电容器高得多。基于 NPPy/CF 的超级电容器还表现出高弯曲和循环稳定性,在 500 次弯曲循环后保留初始电容的 84%,在 5000 次充放电循环后保留初始电容的 91%。

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ACS Omega. 2020 Mar 20;5(12):6441-6451. doi: 10.1021/acsomega.9b04029. eCollection 2020 Mar 31.