Bekyarova Elena, Kalinina Irina, Itkis Mikhail E, Beer Leanne, Cabrera Nelson, Haddon Robert C
Center for Nanoscale Science and Engineering, Department of Chemistry, University of California-Riverside, Riverside, California 92521, USA.
J Am Chem Soc. 2007 Sep 5;129(35):10700-6. doi: 10.1021/ja0703271. Epub 2007 Aug 15.
We provide definitive evidence for the mechanism of electronic detection of ammonia by monitoring in situ changes in the electrical resistance and optical spectra of films of poly(m-aminobenzenesulfonic acid)-functionalized SWNTs (SWNT-PABS). The increase of resistance during exposure to ammonia is associated with deprotonation of the PABS side chain that in turn induces electron transfer between the oligomer and the valence band of the semiconducting SWNTs. Near IR spectroscopy is used to demonstrate that the charge transfer is a weakly driven process, and this accounts for the high reversibility of the sensor. We show that the sensitivity of the chemiresistors increases as the film thickness is reduced to the percolation threshold and that the SWNT-PABS film thickness provides a simple means to enhance the electronic response.
通过监测聚(间氨基苯磺酸)功能化单壁碳纳米管(SWNT-PABS)薄膜的电阻和光谱的原位变化,我们为氨的电子检测机制提供了确凿证据。暴露于氨期间电阻的增加与PABS侧链的去质子化有关,这反过来又诱导了低聚物与半导体单壁碳纳米管价带之间的电子转移。近红外光谱用于证明电荷转移是一个弱驱动过程,这解释了传感器的高可逆性。我们表明,随着薄膜厚度减小到渗流阈值,化学电阻器的灵敏度会增加,并且SWNT-PABS薄膜厚度提供了一种增强电子响应的简单方法。