One-step, template-free synthesis of highly porous nitrogen/sulfur-codoped carbons from a single protic salt and their application to CO2 captureElectronic supplementary information (ESI) available. See DOI: 10.1039/c5ta03575a

Traditional methods for preparing highly porous, nitrogen/sulfur-codoped carbons require either template-based tedious, time-consuming procedures or harsh chemical/physical activation processes. In this paper, we report a very facile method to prepare such carbons via the direct carbonization of a s...

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Bibliographic Details
Main Authors Zhang, Shiguo, Li, Zhe, Ueno, Kazuhide, Tatara, Ryoichi, Dokko, Kaoru, Watanabe, Masayoshi
Format Journal Article
LanguageEnglish
Published 18.08.2015
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Summary:Traditional methods for preparing highly porous, nitrogen/sulfur-codoped carbons require either template-based tedious, time-consuming procedures or harsh chemical/physical activation processes. In this paper, we report a very facile method to prepare such carbons via the direct carbonization of a single protic salt, prop-2-en-1-aminium hydrogensulfate, in the absence of any hard/soft template or activation agent. Depending on the carbonization temperatures, the obtained carbons exhibited tunable structures and properties, in terms of their morphologies, surface areas, pore structures, and chemical compositions. Particularly, the carbon material obtained at 1000 °C had a very large surface area (1149 m 2 g −1 ), even comparable to that of traditionally activated carbon. Among all the samples, the carbon obtained at 900 °C, exclusively having a narrowly distributed microporous structure, exhibited a significant CO 2 uptake of 2.58 mmol g −1 at 298 K and 1 atm. This carbon could also be easily regenerated and reused without any evident loss of CO 2 -adsorption capacity. Highly porous N/S-codoped carbons obtained by one-step carbonization of an "all-in-one" protic salt showed great potential for CO 2 capture.
Bibliography:10.1039/c5ta03575a
Electronic supplementary information (ESI) available. See DOI
ISSN:2050-7488
2050-7496
DOI:10.1039/c5ta03575a