The development of carbon nanotube-(CNTs-)based gas sensors and sensor arrays has attracted intensive research interest in the last several years because of their potential for the selective and rapid detection of various gaseous species by novel nanostructures integrated in miniature and low-power consuming electronics. Chemiresistors and chemical field effect transistors are probably the most promising types of gas nanosensors. In these sensors, the electrical properties of nanostructures are dramatically changed when exposed to the target gas analytes. In this review, recent progress on the development of different types of CNT-based nanosensors is summarized. The focus was placed on the means used by various researchers to improve the sensing performance (sensitivity, selectivity and response time) through the rational functionalization of CNTs with different methods (covalent and non-covalent) and with different materials (polymers and metals).
We review recent advances in biosensors based on one-dimensional (1-D) nanostructure field-effect transistors (FET). Specifically, we address the fabrication, functionalization, assembly/alignment and sensing applications of FET based on carbon nanotubes, silicon nanowires and conducting polymer nanowires. The advantages and disadvantages of various fabrication, functionalization, and assembling procedures of these nanosensors are reviewed and discussed. We evaluate how they have been used for detection of various biological molecules and how such devices have enabled the achievement of high sensitivity and selectivity with low detection limits. Finally, we conclude by highlighting some of the challenges researchers face in the 1-D nanostructures research arena and also predict the direction toward which future research in this area might be directed.
We developed a simple and cost-effective fabrication technique to construct a hydrogen nanosensor by decorating single-walled carbon nanotubes with Pd nanoparticles. By varying the sensor's synthesis conditions (e.g., Pd electrodeposition charge, deposition potential, and initial baseline resistance of the SWNT network), the sensing performance was optimized. The optimized sensor showed excellent sensing properties toward hydrogen (ΔR/R of 0.42%/ppm) with a lower detection limit of 100 ppm and a linear response up to 1000 ppm. The response time decreased from tens of minutes to a few minutes with increasing hydrogen concentration at room temperature. The sensor's recovery time improved under humid air conditions compared to dry air conditions.
A simple, one-step method for fabricating single biologically functionalized conducting-polymer (polypyrrole) nanowire on prepatterned electrodes and its application to biosensing was demonstrated. The biologically functionalized polypyrrole was formed by the electropolymerization of an aqueous solution of pyrrole monomer and the model biomolecule, avidin- or streptavidin-conjugated ZnSe/CdSe quantum dots, within 100 or 200 nm wide by 3 mum long channels between gold electrodes on prefabricated silicon substrate. When challenged with biotin-DNA, the avidin- and streptavidin-polypyrrole nanowires generated a rapid change in resistance to as low as 1 nM, demonstrating the utility of the biomolecule-functionalized nanowire as biosensor. The method offers advantages of direct incorporation of functional biological molecules into the conducting-polymer nanowire during its synthesis, site-specific positioning, built-in electrical contacts, and scalability to high-density nanoarrays over the reported silicon nanowire and carbon nanotube biosensors.
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