Highly Microporous Nitrogen-doped Carbon Synthesized from Azine-linked Covalent Organic Framework and its Supercapacitor Function

Gayoung Kim, Jun Yang, Naotoshi Nakashima, Tomohiro Shiraki

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Porous carbons with nitrogen-doped (N-doped) structures are promising materials for advanced energy conversion and storage applications, including supercapacitors and fuel cell catalysts. In this study, microporous N-doped carbon was successfully fabricated through carbonization of covalent organic frameworks (COFs) with an azine-linked two-dimensional molecular network (ACOF1). In the carbonized ACOF1, micropores with diameters smaller than 1 nm are selectively formed, and a high specific surface area (1596 cm2 g−1) is achieved. In addition, the highly porous structure with N-doped sites results in enhancement of the electrochemical capacitance. Detailed investigation for the micropore-forming process reveals that the formation of nitrogen gas during the thermal degradation of the azine bond contributes to the microporous structure formation. Therefore, the present direct carbonization approach using COFs allows the fabrication of microporous heteroatom-doped carbons, based on molecularly designed COFs, toward future electrochemical and energy applications.

Original languageEnglish
Pages (from-to)17504-17510
Number of pages7
JournalChemistry - A European Journal
Volume23
Issue number69
DOIs
Publication statusPublished - Dec 11 2017

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Nitrogen
Carbon
Carbonization
Energy conversion
Specific surface area
Energy storage
Fuel cells
Pyrolysis
Capacitance
Gases
Fabrication
Catalysts
Supercapacitor

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry

Cite this

Highly Microporous Nitrogen-doped Carbon Synthesized from Azine-linked Covalent Organic Framework and its Supercapacitor Function. / Kim, Gayoung; Yang, Jun; Nakashima, Naotoshi; Shiraki, Tomohiro.

In: Chemistry - A European Journal, Vol. 23, No. 69, 11.12.2017, p. 17504-17510.

Research output: Contribution to journalArticle

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