正硅酸乙酯
共聚物
材料科学
环氧乙烷
化学工程
碳化
胶体二氧化硅
间苯二酚
环氧丙烷
溶解
碳纤维
氧化物
多孔性
高分子化学
有机化学
化学
纳米技术
聚合物
复合材料
扫描电子显微镜
冶金
工程类
复合数
涂层
作者
Joanna Górka,Mietek Jaroniec
出处
期刊:Carbon
[Elsevier]
日期:2010-09-08
卷期号:49 (1): 154-160
被引量:124
标识
DOI:10.1016/j.carbon.2010.08.055
摘要
A series of hierarchically porous carbons was synthesized by self-assembly of polymeric carbon precursors and block copolymer template in the presence of tetraethyl orthosilicate (TEOS) and colloidal silica under acidic conditions. Resorcinol and formaldehyde were used as carbon precursors, poly(ethylene oxide)–poly(propylene oxide)–poly(ethylene oxide) triblock copolymer was employed as a soft template, and TEOS-generated silica and colloidal silica were used as hard templates. The carbon precursors were polymerized in hydrophilic domains of block copolymer, followed by carbonization and silica dissolution. This resulted in carbons possessing cylindrical (∼12 nm) and spherical (20 or 50 nm) mesopores created by thermal decomposition of the soft template and by the dissolution of colloidal silica, respectively; fine pores were also formed by the dissolution of the TEOS-generated silica (∼2 nm). A further increase in fine porosity was achieved by post-synthesis activation of the carbons with carbon dioxide and/or water vapor, which resulted in hierarchical carbons with a surface area and pore volume approaching 2800 m2/g and 6.0 cm3/g, respectively.
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