Capillary shrinkage of graphene oxide hydrogels

被引:42
|
作者
Qi, Changsheng [1 ,4 ]
Luo, Chong [2 ]
Tao, Ying [1 ,4 ]
Lv, Wei [2 ]
Zhang, Chen [3 ]
Deng, Yaqian [2 ]
Li, Huan [1 ,4 ]
Han, Junwei [1 ,4 ]
Ling, Guowei [3 ]
Yang, Quan-Hong [1 ,4 ]
机构
[1] Tianjin Univ, Nanoyang Grp, State Key Lab Chem Engn, Sch Chem Engn & Technol,Collaborat Innovat Ctr Ch, Tianjin 300350, Peoples R China
[2] Tsinghua Univ, Shenzhen Geim Graphene Ctr & Engn Lab Functionali, Grad Sch Shenzhen, Shenzhen 518055, Peoples R China
[3] Tianjin Univ, Sch Marine Sci & Technol, Tianjin 300350, Peoples R China
[4] Int Campus Tianjin Univ, Joint Sch Natl Univ Singapore & Tianjin Univ, Fuzhou 350207, Peoples R China
基金
中国国家自然科学基金;
关键词
graphene oxides; porous carbons; hydrogels; capillary force; network shrinkage; ELECTROCHEMICAL PERFORMANCE; VOLUMETRIC CAPACITANCE; POROUS CARBONS; SUPERCAPACITORS; SULFUR; ELECTRODES; NITROGEN; AEROGELS; WATER; DENSE;
D O I
10.1007/s40843-019-1227-7
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Conventional carbon materials cannot combine high density and high porosity, which are required in many applications, typically for energy storage under a limited space. A novel highly dense yet porous carbon has previously been produced from a three-dimensional (3D) reduced graphene oxide (r-GO) hydrogel by evaporation-induced drying. Here the mechanism of such a network shrinkage in r-GO hydrogel is specifically illustrated by the use of water and 1,4-dioxane, which have a sole difference in surface tension. As a result, the surface tension of the evaporating solvent determines the capillary forces in the nanochannels, which causes shrinkage of the r-GO network. More promisingly, the selection of a solvent with a known surface tension can precisely tune the microstructure associated with the density and porosity of the resulting porous carbon, rendering the porous carbon materials great potential in practical devices with high volumetric performance.
引用
收藏
页码:1870 / 1877
页数:8
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