Edilene Assunção da Silva

Hydrogen sulfide (H₂S) gas poses a significant risk and thus demands continuous monitoring using reliable sensors. Chemiresistive sensors can serve this purpose, and the utilization of conducting polymeric materials, particularly polyaniline (PAni), has demonstrated significant potential. To fabricate chemiresistors based on PAni, the materials must be dispersed in an organic solvent like dimethylformamide (DMF), which has several hazardous properties. Fortunately, dimethyl sulfoxide (DMSO) is a safer alternative with similar properties to DMF, and may be used instead of DMF. In this study, we aim to compare the efficacy of DMF and DMSO solvents in fabricating PAni and metal chloride composite films for detecting H₂S gas.

Three solvents were used to solubilize PCBM-based materials, with and without P3HT, and Langmuir techniques were used to identify their impact on film and nano-domain formation, revealing in-depth understanding of the impact of solvents on morphology.

The discrimination of humidity in exhaled breath is of utmost importance to turn breath analysis into an efficient noninvasive tool for early diagnosis or treatment monitoring of several diseases. Herein, by assembling different ratios of the conductive poly(3,4‐ethylenedioxythiophene): polystyrene sulfonate with the polymer matrix polyethylene oxide (PEO), humidity chemiresistor‐based sensors are designed and investigated. The testing results display a broad relative humidity detection range (6–92%), repeatability, reproducibility, and good reversibility. Meanwhile, the sensors possess good reliability for distinct temperatures and in the presence of typical volatile organic compounds found in human exhaled air. The hygroscopic idiosyncrasy of PEO is attributed to be the main responsible for the high sensibility toward humidity. In a proof‐of‐principle for detection of respiration humidity, the outcome shows the ability of the chemiresistors to detect the humidity variation in a real case of breath exposure up to 2 s intervals. The 30 d trial of stability readings shows a standard deviation of only 2.6%. These sensing devices appear as a new array component able to distinguish moisture from biomarkers of diagnosed diseases in breath analysis.

Low-bandgap polymers are widely used as p-type components in photoactive layers of organic solar cells, due to their ability to capture a large portion of the solar spectrum. The comprehension of their supramolecular assembly is crucial in achieving high-performance organic electronic devices. Here we synthezed two exemplar low-bandgap cyclopentadithiophene (CPDT):diketopyrrolopyrrole (DPP)-based polymers, with either a twelve carbon (C12) or a tri etyleneglycol (TEG) side chains on the DPP units (respectively denoted PCPDTDPP_C12 and PCPDTDPP_TEG). We deposited Langmuir-Schaefer films of these polymers blended with the widely used electron donor material [6,6]-phenyl-C61-butyric-acid methyl ester (PCBM). We then characterized the conformational, optical and morphological properties of these films. From the monolayers to the solid films, we observed distinct self-organization and surface properties for each polymer due to the distinct nature of their side chains. Emphasizing their attraction interactions with PCBM and the phase transitions according to the surface pressure. The elements amount on the surface, calculated through the XPS, gave us a good insight on the polymers’ conformations. Through UV-visible absorption spectroscopy, the improvement in the PCPDTDPP film ordering upon PCBM addition is evident and we saw the contribution of the polymer units on the optical response. Chemical attributions of the polymers were assigned using FTIR Spectroscopy and Raman Scattering, revealing the physical interaction after mixing the materials. We showed that it is possible to build nanostructured PCPDTDPPs films with a high control of their molecular properties through an understanding of their self-assembly and interactions with an n-type material.

Polythiophene thin films are widely studied for applications in organic electronics. However, some comparisons are still missing, regarding distinct deposition techniques and regioregularity. Here regioregular and regiorandom alkyl-substituted polythiophene derivatives (P3ATs) were deposited on solid substrates using both Langmuir-Blodgett (LB) and Langmuir-Schaefer (LS) techniques. The main goal was to verify the possible influence of the regioregularity as well the deposition technique on their optical, electrical and electrochemical properties. LB and LS films of regioregular and regiorandom poly(3-butylthiophene) (P3BT) and poly(3-octylthiophene) (P3OT) were deposited onto glass/Indium-Tin-Oxide) substrates and characterized by UV-visible optical spectroscopy, atomic force microscopy, cyclic voltammetry, and conductivity measurements. The results demonstrated the influence of the deposition technique on the electrical outcome, moreover, the regioregularity affected all the performed characterizations. In addition, this paper may be useful to understand how the amphiphilic molecule addition affected the film properties of regioregular and regiorandom P3ATs, particularly the energy diagram provided by the electrochemical and absorption features.