Conductive Polymer Composites for Hydrogen Sulphide Sensors Working at Sub-PPM Level and Room Temperature.

Hybrid composites based on tin chloride and the conductive polymers, polyaniline (PAni) and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS), were integrated into high-performance hydrogen sulphide (H2S) gas sensors working at room temperature. The morphology and chemical properties were studied by scanning and transmission electron microscopy (SEM, TEM), energy dispersive spectroscopy (EDS) and Fourier-transform infrared (FTIR). The composites demonstrated a slightly porous nanostructure and strong interactions between the polymers and the metal salt, which slightly dopes PAni. The hybrid sensors exhibited a very low detection limit (<85 ppb), fast response, repeatability, reproducibility and stability over one month. Moreover, this work presents how calibration based on the derivative of the signal can give hybrid sensors the ability to quantify the concentration of targeted gas, even during continuous variation of the analyte concentration. Finally, the effect of interfering species, such as water and ammonia, is discussed.

Facile Fabrication of an Ammonia-Gas Sensor Using Electrochemically Synthesised Polyaniline on Commercial Screen-Printed Three-Electrode Systems.

Polyaniline (PANI) is a conducting polymer, widely used in gas-sensing applications. Due to its classification as a semiconductor, PANI is also used to detect reducing ammonia gas (NH3), which is a well-known and studied topic. However, easier, cheaper and more straightforward procedures for sensor fabrication are still the subject of much research. In the presented work, we describe a novel, more controllable, synthesis approach to creating NH3 PANI-based receptor elements. The PANI was electrochemically deposited via cyclic voltammetry (CV) on screen-printed electrodes (SPEs). The morphology, composition and surface of the deposited PANI layer on the Au electrode were characterised with electron microscopy, Fourier-transform infrared spectroscopy and profilometry. Prior to the gas-chamber measurement, the SPE was suitably modified by Au sputtering the individual connections between the three-electrode system, thus showing a feasible way of converting a conventional three-electrode electrochemical SPE system into a two-electrode NH3-gas detecting system. The feasibility of the gas measurements' characterisation was improved using the gas analyser. The gas-sensing ability of the PANI-Au-SPE was studied in the range 32-1100 ppb of NH3, and the sensor performed well in terms of repeatability, reproducibility and sensitivity.

Influence of Dispersed Nanoparticles on the Kinetics of Formation and Molecular Mass of Polyaniline.

Using a combination of the open circuit potential and pH profiles of aniline (An) polymerization and their mathematical treatment, we develop a new convenient semiquantitative approach to determine the influence of the dispersed nanoparticles (e.g., TiO2 nanoparticles) on the kinetic features of this process and molecular mass of the formed polyaniline (PANI). It is revealed that the reciprocal values of the polymerization stages, namely, the duration of the induction period, of homogeneous and heterogeneous pernigraniline (PN) accumulation, and of PN reduction with An, are linear functions of the weight fraction of the nanoparticles. We found that when nanoparticles are added the weight-averaged molecular weight of PANI initially increases from 56 000 to 79 000 and the polydispersity index drops from 3.9 to 1.7. However, at high TiO2 concentrations, the former dramatically decreases, whereas the latter increases. We use the relative proton concentration as a function of time and the different extents of acceleration of the consecutive stages of An polymerization to explain the changes in the molecular weight distribution of PANI with different contents of TiO2 nanoparticles in the polymerization medium.