Porous Carbon Nanofibers with Heteroatoms Doped by Electrospinning Exhibit Excellent Acetone and Carbon Dioxide Adsorption Performance: The Contributions of Pore Structure and Functional Groups

被引:9
作者
Shi, Rui [1 ,2 ]
Liu, Baogen [1 ]
Jiang, Yuwei [1 ]
Xu, Xiang [1 ]
Wang, Huijun [1 ]
Zeng, Zheng [1 ]
Li, Liqing [1 ]
机构
[1] Cent South Univ, Sch Energy Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Inner Mongolia Univ Technol, Sch Civil Engn, Hohhot 010051, Inner Mongolia, Peoples R China
来源
ACS OMEGA | 2021年 / 6卷 / 45期
基金
中国国家自然科学基金;
关键词
OXIDE COMPOSITES; CO2; UPTAKE; NITROGEN; ACTIVATION; ADSORBENTS; MICROPORES; CHEMISTRY; FIBERS; RESIN;
D O I
10.1021/acsomega.1c04618
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Rich chemical properties and a well-developed pore structure are the key factors of porous materials for gas storage. Herein, rich heteroatom-doped porous carbon nanofibers (U1K2-X) with a large surface area were prepared by electrospinning followed by potassium hydroxide (KOH) activation. Low-cost urea was chosen as the nitrogen source and structural guiding agent. U1K2-X have a high specific surface area (628-2688 m(2) g(-1)), excellent pore volume (0.468-1.571 cm(3) g(-1)), and abundant nitrogen (2.5-12.8 atom %) and oxygen (4.5-12.5 atom %) contents. Acetone and carbon dioxide were used as target adsorbents to evaluate the adsorption properties of U1K2-X by experiments. These U1K2-X exhibit excellent adsorption performance (260.03-955.74 mg g(-1), 25 degrees C, 18 kPa) and multilayer adsorption (the adsorption layer number n > 2) for acetone, which is mainly attributed to the large specific surface area and pore volume. Besides this, the carbon dioxide uptake reached 2.73-3.34 mmol g(-1) at 25 degrees C. This was attributed to the combination of high nitrogen-oxygen contents and microporous structure. Furthermore, U1K2-X show the desirable repeatability. This study provides a new direction for the preparation of heteroatom-doped porous carbon nanofibers, which will be a promising material for gas adsorption.
引用
收藏
页码:30716 / 30725
页数:10
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