Graphene Dissolution at High Concentrations and Formation of Liquid Crystals

Tuesday, November 10, 2009: 3:35 PM
Magnolia Boardroom B (Gaylord Opryland Hotel)

Natnael Behabtu, Chemical and Biomolecular Engineering, Rice University, Houston, TX
Jay R. Lomeda, Chemistry, Rice University, Houston, TX
Micah J. Green, Chemical and Biomolecular Engineering, Rice University, Houston, TX
Dmitry V. Kosynkin, Chemistry, Rice University, Houston, TX
Amanda Higginbotham, Chemistry, Rice University, Houston, TX
Colin C. Young, Chemical and Biomolecular Engineering, Rice University, Houston, TX
Nicholas G. Parra-Vasquez, Chemical and Biomolecular Engineering, Rice University, Houston, TX
Judith Schmidt, Chemical Engineering, Technion-Israel Institute of Technology, Haifa 32000, Israel
Ellina Kesselman, Chemical Engineering, Technion-Israel Institute of Technology, Haifa 32000, Israel
Yeshayahu Talmon, Chemical Engineering, Technion-Israel Institute of Technology, Haifa 32000, Israel
James M. Tour, Chemistry, Rice University, Houston, TX
Matteo Pasquali, Chemical and Biomolecular Engineering, Rice University, Houston, TX

Graphene is a promising new material with a wide number of potential applications, including electronics and nanocomposites, which often require that the graphene be dispersed and processed as single layers in a fluid phase. Here we show that in chlorosulfonic acid, pristine graphene is spontaneously exfoliated and dissolved at isotropic concentrations as high as ~1000 ppm without the need for covalent functionalization, surfactant stabilization, or sonication. At higher concentration, a liquid-crystalline phase spontaneously forms. Cryo-TEM and AFM show evidence of single-layer to few-layer dissolution. We show that these isotropic and liquid crystalline phases can be leveraged for making flexible electronics as well as multifunctional fibers.
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