Hierarchical Porous Carbon Foams Synthesized by Highly Efficient Microwave Pyrolysis for Supercapacitors

超级电容器 热解 多孔性 微波食品加热 材料科学 化学工程 碳纤维 多孔介质 纳米技术 电容 化学 复合材料 复合数 电极 计算机科学 电信 物理化学 工程类
作者
Zhenlu Liu,Xuan Luo,Yongshuo Peng,Shuijian He,Cheng Song,Chunmei Zhang,Zhen Yin,Zhiqiang Sun,Haoqi Yang,Qian Zhang
出处
期刊:Langmuir [American Chemical Society]
标识
DOI:10.1021/acs.langmuir.5c03489
摘要

Carbon, as an ideal electrode material for supercapacitors, plays an indelible role in the development of energy storage. Sufficient specific surface area, suitable pore distribution, and disordered graphite-like domains are the three factors that coregulate the double-layer capacitance of carbon. However, the preparation of porous carbon is still limited to uneconomical fossil raw materials, complex energy-consuming carbonization processes, and unsatisfactory properties. With the improvement of people's requirements for supercapacitors, efficient, fast, and energy-saving carbon preparation has become a key research direction of supercapacitors. In this paper, a simple and fast microwave pyrolysis method was designed to prepare porous carbon materials by using potassium citrate as a carbon source and sodium chloride as a protective molten salt. The designed electrodes have a disordered carbon layer spacing structure and a uniform distribution of micropores, which benefit from thermal diffusion from inside to outside by microwave heating and the high-frequency vibration pyrolysis mode at the molecular level. The reaction time of a few minutes can make the specific surface area of activated carbon reach 1316 m2 g–1. The mass-specific capacitance of the sample in the three-electrode system is 302 F g–1 (0.1 A g–1), and the assembled device can be used after 10,000 charge and discharge cycles and maintains a high capacitance retention rate (76.39%). The preparation method conforms to the concept of "green chemistry", promotes the revelation of the mechanism of the microwave chemical reaction system, and has visible practical production potential.
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