Herein, we demonstrate that highly sensitive conductometric gas nanosensors for H 2 S can be synthesized by electrodepositing gold nanoparticles on single-walled carbon nanotube (SWNT) networks. Adjusting the electrodeposition conditions allowed for tuning of the size and number of gold nanoparticles deposited. The best H 2 S sensing performance was obtained with discrete gold nanodeposits rather than continuous nanowires. The gas nanosensors could sense H 2 S in air at room temperature with a 3 ppb limit of detection. The sensors were reversible, and increasing the bias voltage reduced the sensor recovery time, probably by local Joule heating. The sensing mechanism is believed to be based on the modulation of the conduction path across the nanotubes emanating from the modulation of electron exchange between the gold and carbon nanotube defect sites when exposed to H 2 S.Sensitive detection and monitoring of gaseous reduced sulfur compounds such as hydrogen sulfide (H 2 S) is important because of toxicity, corrosion, and odor nuisance concerns. H 2 S is generated in large amounts in coal and natural gas processing, petroleum industries, biogas production, and sewage treatment plants. 1 The odor threshold of H 2 S is around 3 ppb in air which is well below any known toxic effects, while the threshold limit value (TLV) was set to 10 ppm; at concentrations exceeding 150 ppm, H 2 S is extremely toxic and hazardous. 2 Hence, it is important to develop sensors that can monitor H 2 S in real time and can detect concentrations from as low as a few parts per billion to the several hundred parts per million in air. A number of H 2 S detection techniques have been developed in the past few decades, with electrochemical detection as the most widely utilized method in compact and portable H 2 S gas monitors. 3,4 These devices often rely on solid state sensors made of semiconducting metal oxides such as tungsten oxide and tin oxide or metals such as gold. H 2 S detection is usually based on determining conductivity changes of thin films upon exposure to H 2 S gas. 4,5 While there are a number of successful devices available commercially, drawbacks of existing H 2 S monitors include high power consumption (e.g., in metal oxide sensors that require high operating temperatures); low sensitivity, making them unsuitable for environmental monitoring; short lifetime (usually less than one year); short linear dynamic range; interference from other gases (e.g., NH 3 , NO x , etc); and high cost. 6 Recently, chemical sensors based on one-dimensional nanostructures such as bare or functionalized semiconducting singlewalled carbon nanotubes (SWNTs), 6,7 metal oxides, and conducting polymer nanowires 8 have attracted a great deal of attention because of their superior sensing performance. In particular, these sensors offer promising perspectives for real-time monitoring of gases or vapors with high sensitivity and low-power consumption and potentially at a low cost. 6 Their small size will also allow future integration with low-pow...
Magnetic alignment is reported as a facile technique for assembling nanowires into hierarchical structures. Cross junction and T junction nanowire networks are demonstrated using a sequential alignment technique on unpatterned substrates and predefined lithographically patterned ferromagnetic electrodes. The formation of T junctions prevails as nanowires from the first alignment behave as ferromagnetic electrodes under the external magnetic field of the second alignment. The presence of prefabricated ferromagnetic electrodes dominates dipole interactions of localized nanowires for preferential alignment. Application of a magnetic field from a cylindrical coaxial magnet has also been utilized to form radially aligned nanowires. The magnetic field of the coaxial cylindrical magnet produced a dense, concentric nanowire configuration at the centre of the magnetic field as a consequence of the radial field gradient, and sparse nanowire arrangements in the peripheral field, which were utilized as interconnects with a concentric electrode design.
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