HOUSTON (Nov. 29, 2011) The future brightened for organic chemistry when researchers at Rice University found a highly controllable way to attach organic molecules to pristine graphene, making the miracle material suitable for a range of new applications.
The Rice lab of chemist James Tour, building upon a set of previous finds in the manipulation of graphene, discovered a two-step method that turned what was a single-atom-thick sheet of carbon into a superlattice for use in organic chemistry. The work could lead to advances in graphene-based chemical sensors, thermoelectric devices and metamaterials.
The work appeared this week in the online journal Nature Communications.
Graphene alone is inert to many organic reactions and, as a semimetal, has no band gap; this limits its usefulness in electronics. But the project led by the Tour Lab's Zhengzong Sun and Rice graduate Cary Pint, now a researcher at Intel, demonstrated that graphene, the strongest material there is because of the robust nature of carbon-carbon bonds, can be made suitable for novel types of chemistry.
Until now there was no way to attach molecules to the basal plane of a sheet of graphene, said Tour, Rice's T.T. and W.F. Chao Chair in Chemistry as well as a professor of mechanical engineering and materials science and of computer science. "They would mostly go to the edges, not the interior," he said. "But with this two-step technique, we can hydrogenate graphene to make a particular pattern and then attach molecules to where those hydrogens were.
"This is useful to make, for example, chemical sensors in which you want peptides, DNA nucleotides or saccharides projected upward in discrete places along a device. The reactivity at those sites is very fast relative to placing molecules just at the edges. Now we get to choose where they go."
The first step in the process involved creating a lithographic pattern to induce the attachment
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