One-step, template-free synthesis of highly porous nitrogen/sulfur-codoped carbons from a single protic salt and their application to CO2 capture

被引:35
作者
Zhang, Shiguo [1 ]
Li, Zhe [1 ]
Ueno, Kazuhide [1 ]
Tatara, Ryoichi [1 ]
Dokko, Kaoru [1 ]
Watanabe, Masayoshi [1 ]
机构
[1] Yokohama Natl Univ, Dept Chem & Biotechnol, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
基金
日本科学技术振兴机构;
关键词
METAL-FREE ELECTROCATALYSTS; DOPED MICROPOROUS CARBONS; OXYGEN REDUCTION; MESOPOROUS CARBONS; IONIC LIQUIDS; SURFACE-AREA; ORGANIC FRAMEWORK; PERFORMANCE; ADSORPTION; PRECURSORS;
D O I
10.1039/c5ta03575a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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 degrees 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 degrees C, exclusively having a narrowly distributed microporous structure, exhibited a significant CO2 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 CO2-adsorption capacity.
引用
收藏
页码:17849 / 17857
页数:9
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