气凝胶
石墨烯
材料科学
电催化剂
氧化物
化学工程
乙腈
碳纤维
电化学
纳米技术
电极
有机化学
化学
复合材料
复合数
工程类
物理化学
冶金
作者
Matthew B. Lim,Matthew Hu,Sandeep Manandhar,Avery Sakshaug,Adam Strong,Leah Riley,Peter J. Pauzauskie
出处
期刊:Carbon
[Elsevier BV]
日期:2015-08-15
卷期号:95: 616-624
被引量:98
标识
DOI:10.1016/j.carbon.2015.08.037
摘要
Graphene aerogels derived from graphene-oxide (GO) starting materials recently have been shown to exhibit a combination of high electrical conductivity, chemical stability, and low cost that has enabled a range of electrochemical applications. Standard synthesis protocols for manufacturing graphene aerogels require the use of sol–gel chemical reactions that are maintained at high temperatures for long periods of time ranging from 12 h to several days. Here we report an ultrafast, acid-catalyzed sol–gel formation process in acetonitrile in which wet GO-loaded gels are realized within 2 h at temperatures below 45 °C. Spectroscopic and electrochemical analysis following supercritical drying and pyrolysis confirms the reduction of the GO in the aerogels to sp2 carbon crystallites with no residual carbon–nitrogen bonds from the acetonitrile or its derivatives. This rapid synthesis enhances the prospects for large-scale manufacturing of graphene aerogels for use in numerous applications including sorbents for environmental toxins, support materials for electrocatalysis, and high-performance electrodes for electrochemical capacitors and solar cells.
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