Laser-induced carbonization of carbon nanofibers free-standing electrodes for flexible interdigitated micro-supercapacitors

材料科学 超级电容器 石墨烯 纳米纤维 聚丙烯腈 碳化 拉曼光谱 电极 静电纺丝 碳纳米纤维 复合材料 碳纳米管 纳米技术 化学工程 电容 扫描电子显微镜 光学 聚合物 化学 物理 工程类 物理化学
作者
M. Hussein El-Shafei,Mohamed S. Abdel‐Latif,Amr Hessein,Ahmed Abd El‐Moneim
出处
期刊:FlatChem [Elsevier BV]
卷期号:42: 100570-100570 被引量:17
标识
DOI:10.1016/j.flatc.2023.100570
摘要

A versatile one-step laser writing technique is introduced in this work for carbonizing and patterning polymeric nanofibers mat to produce a free-standing laser carbonized nanofibers (LCNFs) electrode for flexible interdigitated microsupercapacitors. A large-area polyacrylonitrile nanofibers mat was first prepared with the facile electrospinning technique on a collecting drum followed by a stabilizing step. A high-power CO2 laser beam is used to carbonize the stabilized nanofibers into highly conductive LCNFs at ambient atmospheric conditions and draw the interdigitated pattern at the same time. The complete carbonization of the nanofibers is confirmed by the nearly complete disappearance of polyacrylonitrile peaks in the FTIR measurements and from the high-intensity characteristic peaks of carbon materials obtained in the Raman scattering measurements of the LCNFs. The SEM microscopy showed that the LCNFs were able to survive their fibrous structure after the laser carbonization process and without any significant damage. Also, the TEM microscopy revealed that the LCNFs are composed of graphene sheets that are axially ordered to form such a unique fibrous structure. Owing to its outstanding structural and electrical properties, the LCNFs interdigitated supercapacitor attained an aerial specific capacitance of 20.38 mF/cm2, a high energy density of 0.64 μWh/cm2, and a high-power density of 224.6 μW/cm2 which are almost two-fold higher than those of the laser-induced graphene (LIG) on a polyamide substrate assembled with the same conditions. This was accompanied by an excellent capacitance retention of 95.3 % after 10,000 electrochemical cyclic stability and impressive mechanical stability and flexibility.
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