Salt-assisted pyrolysis of covalent organic frameworks to porous heteroatom-doped carbons for supercapacitive energy storage

Supercapacitors have attracted intensive research interest due to their advantages including longer cycling ability and higher power density. Porous heteroatom-doped carbons (PHCs) have been regarded as a class of promising electrode materials for supercapacitors because of their unique porous, elec...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019, Vol.7 (47), p.26829-26837
Hauptverfasser: Yan, Dongwan, Wu, Yang, Kitaura, Ryo, Awaga, Kunio
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Sprache:eng
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Zusammenfassung:Supercapacitors have attracted intensive research interest due to their advantages including longer cycling ability and higher power density. Porous heteroatom-doped carbons (PHCs) have been regarded as a class of promising electrode materials for supercapacitors because of their unique porous, electronic and chemical properties. However, synthesis of PHCs with hierarchical mesoporous/microporous structures and ultra-high porosity and electrochemical performance remains a great research challenge. In this research, two oxygen and nitrogen co-doped PHCs (denoted as ONC-T1s) are prepared via a salt-assisted pyrolysis method using covalent organic frameworks (COFs) as the precursor. ONC-T1s show a hierarchical porous structure with an ultra-high specific surface area (up to 3451 m 2 g −1 ). The ONC-T1-850-based supercapacitor exhibits a high specific capacitance of 1711 F g −1 at 1 A g −1 , an ultra-fast charge-discharge rate up to 500 A g −1 with a specific capacitance of 856 F g −1 , and excellent stability. This work establishes a promising strategy for preparation of PHCs using COFs or other porous organic polymers as precursors and demonstrates the great potential of PHC-based supercapacitors. Highly porous heteroatom-doped carbons with ultra-high supercapacitive performance are prepared by salt-assisted pyrolysis of covalent organic frameworks.
ISSN:2050-7488
2050-7496
DOI:10.1039/c9ta05150c