Vapor Sensing Using Conjugated Molecule-Linked Au Nanoparticles in a Silica Matrix

被引:9
|
作者
Dirk, Shawn M. [1 ]
Howell, Stephen W. [2 ]
Price, B. Katherine [3 ,4 ,5 ]
Fan, Hongyou [6 ]
Washburn, Cody [1 ]
Wheeler, David R. [7 ]
Tour, James M. [3 ,4 ,5 ]
Whiting, Joshua [8 ]
Simonson, R. Joseph [8 ]
机构
[1] Sandia Natl Labs, Organ Mat Dept, Albuquerque, NM 87185 USA
[2] Sandia Natl Labs, Advanced Sensor Technol Dept, Albuquerque, NM 87185 USA
[3] Rice Univ, Smalley Inst Nanoscale Sci & Technol, Dept Chem, Houston, TX 77005 USA
[4] Rice Univ, Smalley Inst Nanoscale Sci & Technol, Dept Mech Engn, Houston, TX 77005 USA
[5] Rice Univ, Smalley Inst Nanoscale Sci & Technol, Dept Mat Sci, Houston, TX 77005 USA
[6] Sandia Natl Labs, Ceram Proc & Inorgan Dept, Albuquerque, NM 87185 USA
[7] Sandia Natl Labs, Biosensors & Nanomat Dept, Albuquerque, NM 87185 USA
[8] Sandia Natl Labs, Micrototal Analyt Syst Dept, Albuquerque, NM 87185 USA
关键词
SELF-ASSEMBLED MONOLAYERS; GOLD; SENSOR; FILMS; CHEMIRESISTORS; ARRAYS;
D O I
10.1155/2009/481270
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Cross-linked assemblies of nanoparticles are of great value as chemiresistor-type sensors. Herein, we report a simple method to fabricate a chemiresistor-type sensor that minimizes the swelling transduction mechanism while optimizing the change in dielectric response. Sensors prepared with this methodology showed enhanced chemoselectivity for phosphonates which are useful surrogates for chemical weapons. Chemoselective sensors were fabricated using an aqueous solution of gold nanoparticles that were then cross-linked in the presence of the silica precursor, tetraethyl orthosilicate with the alpha-, omega-dithiolate (which is derived from the in situ deprotection of 1,4-di(Phenylethynyl-4', 4 ''-diacetylthio)-benzene (1) with wet triethylamine). The cross-linked nanoparticles and silica matrix were drop coated onto interdigitated electrodes having 8 mu m spacing. Samples were exposed to a series of analytes including dimethyl methylphosphonate (DMMP), octane, and toluene. A limit of detection was obtained for each analyte. Sensors assembled in this fashion were more sensitive to dimethyl methylphosphonate than to octane by a factor of 1000. Copyright (C) 2009 Shawn M. Dirk et al.
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页数:9
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