Volume 47, Issue 27 pp. 5018-5021
Communication

On-Chip Micro Gas Chromatograph Enabled by a Noncovalently Functionalized Single-Walled Carbon Nanotube Sensor Array

Chang Young Lee

Chang Young Lee

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139 (USA), Fax: (+1) 617-258-8224

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Richa Sharma

Richa Sharma

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139 (USA), Fax: (+1) 617-258-8224

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Adarsh D. Radadia

Adarsh D. Radadia

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801 (USA)

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Richard I. Masel Prof.

Richard I. Masel Prof.

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801 (USA)

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Michael S. Strano Prof.

Michael S. Strano Prof.

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139 (USA), Fax: (+1) 617-258-8224

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First published: 16 June 2008
Citations: 75

This work was supported by the Department of Homeland Security and the Federal Aviation Administration under grant DHS S&T 06-G-026. R. Masel acknowledges funding from Defense Advanced Research Projects Agency (DARPA) under U.S. Air Force grant FA8650-04-1-7121. SEM was carried out in the Center for Microanalysis of Materials, University of Illinois, which is partially supported by the U.S. Department of Energy under grantDEFG02-91-ER45439.

Graphical Abstract

Sensing in reverse: Reversible detection of as few as 109 molecules (1700 aM) of dimethyl methylphosphonate, a nerve agent simulant, is demonstrated at the end of a micro GC column (see picture). Such arrays form the basis of rapidly transducing molecular sensors with micrometer-sized footprints. The separation capability of the column eliminates the need for selectivity on the sensor, as long as analyte binding is reversible and rapid.

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