Electrospun porous carbon nanofibers derived from bio-based phenolic resins as free-standing electrodes for high-performance supercapacitors

Abstract

Phenolic resins were employed to prepare electrospun porous carbon nanofibers with a high specific surface area as free-standing electrodes for high-performance supercapacitors. However, the sustainable development of conventional phenolic resin has been challenged by petroleum-based phenol and formaldehyde. Lignin with abundant phenolic hydroxyl groups is the main non-petroleum resource that can provide renewable aromatic compounds. Hence, lignin, phenol, and furfural were used to synthesize bio-based phenolic resins, and the activated carbon nanofibers were obtained by electrospinning and one-step carbonization activation. Fourier transform infrared and differential scanning calorimetry were used to characterize the structural and thermal properties. The results reveal that the apparent activation energy of the curing reaction is 89.21 kJ·mol^–1 and the reaction order is 0.78. The activated carbon nanofibers show a uniform diameter, specific surface area up to 1100 m²·g^–1, and total pore volume of 0.62 cm³·g^–1. The electrode demonstrates a specific capacitance of 238 F·g^–1 (0.1 A·g^–1) and good rate capability. The symmetric supercapacitor yields a high energy density of 26.39 W·h·kg^–1 at 100 W·kg^–1 and an excellent capacitance retention of 98% after 10000 cycles. These results confirm that the activated carbon nanofiber from bio-based phenolic resins can be applied as electrode material for high-performance supercapacitors.

Graphical abstract

Keywords

lignin / bio-based phenolic resins / electrospinning / activated carbon nanofibers / supercapacitors

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Acknowledgements

This work was supported by the National Natural Science Foundation of China (Grant Nos. 21908204, 52074244) and the Henan Provincial Key Research and Development Program (Grant No. 192102310202). The authors would also like to acknowledge the support from Zhengzhou University.

Electronic Supplementary Material

Supplementary material is available in the online version of this article at https://dx.doi.org/10.1007/s11705-022-2260-1 and is accessible for authorized users.

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