Graphene lights up with new possibilities: Two-step technique makes graphene suitable for organic chemistry

Graphene lights up with new possibilities: Two-step technique makes graphene suitable for organic chemistry:

'via Blog this'

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.

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.