ABSTRACT
The electrospinning technique has been successfully used to prepared micro-fibers of the poly(lactic acid)/polyaniline-zinc oxide (PLA/PANI-ZnO) composite. The polyaniline-zinc oxide (PANI-ZnO) nanocomposites are synthesized by hydrothermal and in situ polymerization methods. X-ray diffraction techniques are used to study the structural properties of the PLA/PANI-ZnO composite fibers and the PANI-ZnO nanocomposite. The average crystallite size of the PANI-ZnO nanocomposite is found to be 36 nm. The morphology and diameter of the composite fibers are analyzed by scanning electron microscopy (SEM). The average fiber diameter of the pure poly(lactic acid) (PLA) fiber is around 2.5 µm and that of the PLA/PANI-ZnO composite fiber is around 1.4 µm. Differential scanning calorimetry (DSC) provides the thermal properties of the PLA/PANI-ZnO composite fibers. The melting temperature (T m) for the pure PLA is observed at 149.3 °C, and it is shifted to 153.0 °C for the PLA/PANI-ZnO composite fibers. The enhanced thermal properties of the composite fibers are due to the interaction between the polymer and the nanoparticles. The water contact angle measurements probe the surface hydrophilicity of the PLA/PANI-ZnO composite fibers. The role of the PANI-ZnO nanocomposite on the sensing behavior of PLA fibers has also been investigated. The humidity sensing properties of the composite fiber based sensor are studied in the relative humidity (RH) range of 20-90% RH. The experimental results show that the composite fiber exhibited good response (85 s) and recovery (120 s) times. These results indicate that the one-dimensional (1D) fiber structure enhances the humidity sensing properties.
ABSTRACT
Porous microstructure materials are considered good candidates for the development of highly sensitive and fast humidity sensors. In this regard, we prepared polyaniline (PANI) decorated Cu-ZnS porous microsphere structures (PMSs) for the fabrication of humidity sensors. PANI coated Cu-ZnS PMSs were synthesized by a hydrothermal method and in situ polymerization process. The synthesized PMSs were characterized by different techniques to study the structural, morphological and surface absorption properties. Several compositions for the PANI/Cu-ZnS PMS were investigated, which were then compared with pure PANI. The experimental observations demonstrate that a PANI/1%Cu-ZnS PMS has better sensitivity, fast response and good stability compared to pure PANI and other PANI/CuZnS compositions. Finally, a PANI/1% Cu-ZnS PMS was found to be optimized for humidity sensors due to its well distributed roughness, porosity and hydrophilicity. The average response and recovery times for PANI/1% Cu-ZnS were found to be 42 s and 24 s, respectively, which outperform recent results.
ABSTRACT
Halloysite-polypyrrole-silver nanocomposite has been prepared via in situ photopolymerizations of pyrrole in the presence of silanized halloysite and silver nitrate as a photoinitiator. The halloysite nanoclay (HNT) was modified using the hydrogen donor silane coupling agent (DMA) in order to provide anchoring sites for the polypyrrole/silver composite (PPy@Ag). The mass loadings for both PPy and Ag have been estimated to be 21 and 26 wt%, respectively. The anchored Ag particles were found in the metallic state. The resulting PPy@Ag-modified silanized HNT has been evaluated for the potential application for impedance humidity sensors. HNT-DMA-PPy@Ag nanocomposite with different weight % of PPy@Ag (0.25 wt%, 0.5 wt%, and 1 wt%) was deposited on the pre-patterned interdigital Indium Tin Oxide (ITO) electrodes by spin coating technique. The addition of Ag nanoparticles within the nanocomposite enhances the hydrophilicity of the sensing film, which improves the sensitivity of the humidity sensors. The HNT-DMA-PPy@Ag (0.5 wt%) nanocomposite-based impedance sensors showed good sensitivity and lowered hysteresis as compared to the other ratios of the composite. The maximum calculated hysteresis loss of the HNT-DMA-PPy@Ag (0.5 wt%)-based humidity sensor is around 4.5% at 80% RH (relative humidity), and the minimum hysteresis loss estimated to be 0.05% at 20% RH levels. The response and recovery time of HNT-DMA-PPy@Ag (0.5 wt%) nanocomposite-based impedance sensors were found to be 30 and 35 s, respectively. The interesting humidity-dependent impedance properties of this novel composite make it promising in humidity sensing.
ABSTRACT
Polyaniline (PANI)/Cu-ZnS composites with porous microspheres are prepared by a hydrothermal and in situ polymerization method. The structural, optical, and morphological properties are characterized by X-ray powder diffraction, FTIR, UV-vis, scanning electron microscope, transmission electron microscope. The XRD results confirmed that the PANI/Cu-ZnS composite is formed. The morphological analyses exhibited that the PANI/Cu-ZnS composite comprises the porous microspherical structures. The emission peaks obtained in photoluminescence spectra confirm the presence of surface defects in the prepared composite. The UV-DRS study shows that the bandgap of the samples is found to decrease for the PANI/Cu-ZnS composite compared to the pure Cu-ZnS sample. The calculated band gap (E g) value of PANI/Cu-ZnS composite is 2.47 eV. Furthermore, the fabricated gas sensor based on PANI/Cu-ZnS can perform at room temperature and exhibits good gas sensing performance toward CO2 gas. In particular, PANI/Cu-ZnS sensor shows good response (31 s) and recovery time (23 s) upon exposure to CO2 gas. The p/n heterojunction, surface defects, and porous nature of the PANI/Cu-ZnS composite microsphere enhanced sensor performance.
