ABSTRACT
A novel, highly sensitive gold nanowire (AuNW) resistive sensor is reported here for humidity sensing in the relative humidity range of 11% to 92% RH as well as for breath sensing. Both humidity and breath sensors are widely needed. Despite a lot of research on humidity and breath sensors, there is a need for simple, inexpensive, reliable, sensitive and selective sensors, which will operate at room temperature. Here we have synthesized gold nanowires by a simple, wet chemical route. The nanowires synthesized by us are 4-7 nm in diameter and a few micrometers long. The nanowires are amine functionalized. The sensor was prepared by drop casting gold nanowires on an alumina substrate to form a AuNW layer with different thicknesses (10, 20, 30 µm). The AuNW sensor is highly selective towards humidity and shows minimum cross sensitivity towards other gases and organic vapors. At an optimum thickness of 20 µm, the humidity sensing performance of the AuNW sensor over 11% to 92% RH was found to be superior to that of 10 and 30 µm thick layers. The response time of the sensor is found to be 0.2 s and the recovery time is 0.3 s. The response of the AuNW sensor was 3.3 MΩ/% RH. Further, the AuNW sensor was tested for sensing human breathing patterns.
ABSTRACT
A simple chemical reduction method was employed to synthesize Cu-Ag and Ag-Cu core-shell nanostructures inside polyvinyl alcohol (PVA) matrix at room temperature. The core-shell nanostructures have been synthesized by varying the two different concentrations (i.e. 0.1 and 0.01 M) of the respective metal ions in equimolar ratios using successive reduction with hydrazine hydrate (HH) as a reducing agent. The core-shell nanostructures have been further characterized by different characterization techniques. The UV-visible spectroscopy exhibit the respective shift in the band positions suggesting the formation of core-shell nanostructures, which was further confirmed by field emission transmission electron microscopy-high-angle-annular dark field elemental mapping. The effect of metal ion concentration of the core-shell nanostructure on various Gram positive and Gram negative bacteria like Escherichia coli, Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa and one fungal species Aspergillus fumigatus was observed by performing MIC and MBC/MFC study. Cu-Ag core-shell nanostructures were found to be effective antibacterial agent against all tested Gram-positive and Gram-negative bacteria, whereas Ag-Cu core-shell nanostructures were more efficient against a particular fungal species known as A. fumigatus. The highest value of MIC (75 µg ml-1) for Ag-Cu 0.1M core shell nanostructures (D1) was noted against S. aureus and E. coli whereas the lowest value (20 µg ml-1) was observed with P. aeruginosa. While in case of Cu-Ag 0.1M core shell nanostructures (E1) the highest value of MIC (100 µg ml-1) was noted against S. aureus and P. aeruginosa whereas the lowest value (15 µg ml-1) was observed with A. fumigatus. Also, field effect scanning electron microscope (FESEM) images of untreated and core-shell nanoparticles treated micro-organisms showed that 0.1 M Ag-Cu and 0.1 M Cu-Ag core-shell nanostructure can successfully break the cell wall of the fungi A. fumigatus and bacteria P. aeruginosa, respectively. Thus the present study concludes that, Cu-Ag & Ag-Cu core-shell nanostructures damage the cell structure of micro-organisms and inhibits their growth. Hence, the present Cu-Ag & Ag-Cu core-shell nanostructure acts as good antimicrobial agent against the bacteria and fungi, respectively.
