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  C2NxO1-x Framework Carbons with Defined Microporosity and Co-doped Functional Pores

Tian, Z., Fechler, N., Oschatz, M., Heil, T., Schmidt, J., Yuan, S., et al. (2018). C2NxO1-x Framework Carbons with Defined Microporosity and Co-doped Functional Pores. Journal of Materials Chemistry A. doi:10.1039/C8TA03213K.

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 Creators:
Tian, Zhihong1, Author           
Fechler, Nina2, Author           
Oschatz, Martin1, Author           
Heil, Tobias3, Author           
Schmidt, Johannes, Author
Yuan, Siguo, Author
Antonietti, Markus4, Author           
Affiliations:
1Martin Oschatz, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_2364733              
2Nina Fechler, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_2173643              
3Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863288              
4Markus Antonietti, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863321              

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 Abstract: Gallic acid and urea are used to produce C2NO materials with rather dined micropores via direct condensation and ring closure. The materials show a unique heterocycle containing carbonaceous structure and features an unusually high content of heteroatoms (nitrogen, oxygen) lining inside the pores, meanwhile having high specific surface area. The multifunctional carbon materials demonstrate good performance for selective CO2 capture resulting from the adjustable porosity and polarizability. In view of the simplicity of the salt flux synthetic method and the advantage of the available sustainable starting synthons, the C2NO framework has potential for use in diverse practical applications.

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 Dates: 2018-09-10
 Publication Status: Published online
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 Identifiers: DOI: 10.1039/C8TA03213K
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Title: Journal of Materials Chemistry A
  Abbreviation : J. Mater. Chem. A
Source Genre: Journal
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Publ. Info: Cambridge, UK : Royal Society of Chemistry
Pages: - Volume / Issue: - Sequence Number: - Start / End Page: - Identifier: ISSN: 2050-7488