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论文类型：期刊论文

发表时间：2013-12-01

发表刊物：ENERGY & ENVIRONMENTAL SCIENCE

收录刊物：SCIE、EI、Scopus

卷号：6

期号：12

页面范围：3740-3747

ISSN号：1754-5692

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 N-2 under dynamic conditions, and easy regeneration. The highest CO2 adsorption capacities can reach 5.67 and 3.54 CO2 molecules per nm(3) pore volume and per nm(2) surface area at 25 degrees C and similar to 1 bar.