Porous carbon nanosheets with precisely tunable thickness and selective CO2 adsorption properties

纳米片 吸附 石墨烯 材料科学 多孔性 化学工程 分子 聚合物 碳纤维 纳米技术 纳米 氧化物 多孔介质 复合材料 有机化学 化学 复合数 工程类 冶金
作者
Guang‐Ping Hao,Zhenyu Jin,Qiang Sun,Xiangqian Zhang,Jintao Zhang,An‐Hui Lu
出处
期刊:Energy and Environmental Science [Royal Society of Chemistry]
卷期号:6 (12): 3740-3740 被引量:172
标识
DOI:10.1039/c3ee41906a
摘要

We report the wet-chemistry synthesis of a new type of porous carbon nanosheet whose thickness can be precisely controlled over the nanometer length scale. This feature is distinct from conventional porous carbons that are composed of micron-sized or larger skeletons, and whose structure is less controlled. The synthesis uses graphene oxide (GO) as the shape-directing agent and asparagine as the bridging molecule that connects the GO and in situ grown polymers by electrostatic interaction between the molecules. The assembly of the nanosheets can produce macroscopic structures, i.e., hierarchically porous carbon monoliths which have a mechanical strength of up to 28.9 MPa, the highest reported for the analogues. The synthesis provides precise control of porous carbons over both microscopic and macroscopic structures at the same time. In all syntheses the graphene content used was in the range 0.5–2.6 wt%, which is significantly lower than that of common surfactants used in the synthesis of porous materials. This indicates the strong shape-directing function of GO. In addition, the overall thickness of the nanosheets can be tuned from 20 to 200 nm according to a fitted linear correlation between the carbon precursor/GO mass ratio and the coating thickness. The porous carbon nanosheets show impressive CO2 adsorption capacity under equilibrium, good separation ability of CO2 from N2 under dynamic conditions, and easy regeneration. The highest CO2 adsorption capacities can reach 5.67 and 3.54 CO2 molecules per nm3 pore volume and per nm2 surface area at 25 °C and ∼1 bar.
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