Studies of the chemical and pore structures of the carbon aerogels synthesized by gelation and supercritical drying in isopropanol

被引:14
|
作者
Fu, RW
Zheng, B
Liu, J
Weiss, S
Ying, JY
Dresselhaus, MS
Dresselhaus, G
Satcher, J
Baumann, T
机构
[1] MIT, Cambridge, MA 02139 USA
[2] Zhongshan Univ, PCFM Lab, Guangzhou 510275, Peoples R China
[3] Duke Univ, Dept Chem, Durham, NC 27708 USA
[4] Lawrence Livermore Natl Lab, Livermore, CA 94551 USA
关键词
carbon aerogel; gelation and drying in isopropanol; chemical structure; pore structure;
D O I
10.1002/app.13474
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The carbon aerogels prepared by a new method through gelation and supercritical drying in isopropanol were characterized by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy, and a surface area analyzer. Their chemical structure, morphology, and pore structure are discussed. We found that all of these carbon aerogel (CA-IPA) samples have almost the same carbon and oxygen elemental states, as well as similar oxygen-containing groups. The curve fitting of the C1s XPS spectra of the samples for characterizing oxygen-containing surface groups can be performed by assuming the peak type to be a Gaussian-Lorentzian Cross Product, but we cannot obtain good results using a Gaussian lineshape. When the mass density of the CA-IPA decreases, the mesopores and macropores of the samples are found to grow, but the size and the shape of individual carbon nanoparticles in various CA-IPA samples do not apparently change. The micropore volume of the CA-IPA samples increases with a decrease in the mass density, while the mesopore volume has a maximum at a certain mass density. The CA-IPA samples have a very narrow micropore distribution at about 0.5 nm. The mesopore distribution of the CA-IPA is widened and the average pore size increases as the mass density of the sample decreases. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:3060 / 3067
页数:8
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