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PANI/Fe-doped CeO 2 nanocomposite was synthesised by the in-situ process. The produced powders were characterised by XRD, XPS, FT-IR, Raman, HRTEM and SEM-EDS tests. The sensors' function was based on PANI/Fe-doped CeO 2 nanocomposite with thin film deposited on top of interdigitated electrodes (IDT). NH 3 detection with PANI/Fe-doped CeO 2 nanocomposite sensor could be successfully performed even at room temperature (RT) and relative humidity of 45 %. Results demonstrated that PANI/Fe-doped CeO 2 might be promising sensing materials for detecting the low NH 3 concentration (ppm). In addition, the sensor is selective to the interfering gases, including CO, CO 2 and NO 2 . This sensor displays acceptable repeatability and stability over time.

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A novel NH3 gas sensor is introduced, employing polyaniline (PANI) with a unique structure called a graft film. The preparation method was simple: polydopamine (PD) was coated on a flexible polyethylene terephthalate (PET) film and PANI graft chains were grown on its surface. This distinctive three-layer sensor showed a response value of 12 for 50 ppm NH3 in a dry atmosphere at 50 °C. This value surpasses those of previously reported sensors using structurally controlled PANI films. Additionally, it is on par with sensors that combine PANI with metal oxide semiconductors or carbon materials, the high sensitivity of which have been reported. To confirm our film's potential as a flexible sensor, the effect of bending on the its characteristics was investigated. This revealed that although bending decreased the response value, it had no effect on the response time or recovery. This indicated that the sensor film itself was not broken by bending and had sufficient mechanical strength.

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This study introduces a novel nanocomposite coating composed of PANI/CeO2 nanocomposite films, aimed at addressing corrosion protection needs. Analysis through FTIR spectra and XRD patterns confirms the successful formation of the nanocomposite films. Notably, the PANI/CeO2 nanocomposite films exhibit a hydrophilic nature. The bandgap energy of the PANI composite film is measured to be 3.74 eV, while the introduction of CeO2 NPs into the PANI matrix reduces the bandgap energy to 3.67 eV. Furthermore, the electrical conductivity of the PANI composite film is observed to be 0.40 S·cm-1, with the incorporation of CeO2 NPs leading to an increase in electrical conductivity to 1.07 S·cm-1. To evaluate its efficacy, electrochemical measurements were conducted to assess the corrosion protection performance. Results indicate a high protection efficiency of 92.25% for the PANI/CeO2 nanocomposite film.

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Perfluoroalkyl substances (PFAS), known as "forever chemicals," are a growing concern in the sphere of human and environmental health. In response, rapid, reproducible, and inexpensive methods for PFAS detection in the environment and home water supplies are needed. We have developed a simple and inexpensive perfluoroalkyl acid detection method based on an electrically read lateral flow assay (e-LFA). Our method employs a fluorous surfactant formulation with undoped polyaniline (F-PANI) fabricated to create test lines for the lateral flow assay. In perfluoroalkyl acid sensing studies, an increase in conductivity of the F-PANI film is caused by acidification and doping of PANI. A conductivity enhancement by 104-fold can be produced by this method, and we demonstrate a limit of detection for perfluorooctanoic acid (PFOA) of 400 ppt and perfluorobutanoic acid of 200 ppt. This method for PFOA detection can be expanded for wide-scale environmental and at-home water testing.

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Polymeric membranes are useful tools for water filtration processes, with their performance strongly dependent on the presence of hydrophilic dopants. In this study, polyaniline (PANI)-capped aluminosilicate (halloysite) nanotubes (HNTs) are dispersed into polyether sulfone (PES), with concentrations ranging from 0.5 to 1.5 wt%, to modify the properties of the PES membrane. Both undoped and HNT-doped PES membranes are investigated in terms of wettability (static and time-dependent contact angle), permeance, mechanical resistance, and morphology (using scanning electron microscopy (SEM)). The higher water permeance observed for the PES membranes incorporating PANI-capped HNTs is, finally, assessed and discussed vis-à-vis the real distribution of HNTs. Indeed, the imaging and characterization in terms of composition, spatial arrangement, and counting of HNTs embedded within the polymeric matrix are demonstrated using non-destructive Micro Particle Induced X-ray Emission (µ-PIXE) and Scanning Transmission Ion Microscopy (STIM) techniques. This approach not only exhibits the unique ability to detect/highlight the distribution of HNTs incorporated throughout the whole thickness of polymer membranes and provide volumetric morphological information consistent with SEM imaging, but also overcomes the limits of the most common analytical techniques exploiting electron probes. These aspects are comprehensively discussed in terms of practical analysis advantages.

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Piezoelectric materials are promising for biomedical applications because they can provide mechanical or electrical stimulations via converse or direct piezoelectric effects. The stimulations have been proven to be beneficial for cell proliferation and tissue regeneration. Recent reports showed that doping different contents of reduced graphene oxide (rGO) or polyaniline (PANi) into biodegradable polyhydroxybutyrate (PHB) enhanced their piezoelectric response, showing potential for biomedical applications. In this study, we aim to determine the correlation between physiochemical properties and the in vitro cell response to the PHB-based composite scaffolds with rGO or PANi. Specifically, we characterized the surface morphology, wetting behavior, electrochemical impedance, and piezoelectric properties of the composites and controls. The addition of rGO and PANi resulted in decreased fiber diameters and hydrophobicity of PHB. The increased surface energy of PHB after doping nanofillers led to a reduced water contact angle (WCA) from 101.84 ± 2.18° (for PHB) to 88.43 ± 0.83° after the addition of 3 wt % PANi, whereas doping 1 wt % rGO decreased the WCA value to 92.56 ± 2.43°. Meanwhile, doping 0.2 wt % rGO into PHB improved the piezoelectric properties compared to the PHB control and other composites. Adding up to 1 wt % rGO or 3 wt % PANi nanofillers in PHB did not affect the adhesion densities of bone marrow-derived mesenchymal stem cells (BMSCs) on the scaffolds. The aspect ratios of attached BMSCs on the composite scaffolds increased compared to the PHB control. The study indicated that the PHB-based composites are promising for potential applications such as regenerative medicine, tissue stimulation, and bio-sensing, which should be further studied.

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This paper proposes a fabrication of a hyper-sensitive amperometric biosensor for paraoxon-ethyl (PE) detection. In this developed biosensor, polyaniline (PANI) and copper oxide (CuO)-based nanocomposite is used as a sensing platform. The homogeneous distribution of CuO onto the PANI matrix enhances the surface area and conductivity of the nanocomposite. Additionally, the PANI produces a compatible environment for enzyme immobilization, which further enhances the rate of electron transfer. For biosensor fabrication, the nanocomposite is deposited electrophoretically onto the ITO glass substrate and immobilization of acetylcholinesterase (AChE) enzyme is conducted onto the fabricated electrode surface. The results validate good reproducibility, good stability, and high selectivity of the fabricated biosensor (AChE/PANI@CuO/ITO). The inhibition rate of paraoxon-ethyl (PE) is recorded in the concentration range of 1-200 nM with a low limit of detection of 0.096 nM or 96 pM. The sensitivity of the developed biosensor is found to be 49.86 µA(nM)-1. The developed biosensor is further successfully accomplished for the detection of PE in real samples like rice and pulse.

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17ß-estradiol is used as a growth and fertility stimulant in the agronomic sector to induce fertility and manipulate reproductive characteristics in animals. However, unintended or unregulated distribution and exposure to even significant low levels of 17ß-estradiol estrogen have detrimental health implication that can lead to reproductive abnormalities and even cancer. This could have severe effect on the ecosystem imbalance, food safety, to such a degree that its health impact necessitates rapid methods to probe for its prevalence and occurrence in the environment. Herein a simple, robust, sensitive and once-off use electrochemical biosensor to detect 17ß-estradiol is developed, using 3-mercaptopropionic acid capped zinc selenide quantum dots trapped within the polyaniline (PANI) framework structure. The biosensor's interaction with the substrate was based on the capability of the hemeprotein, horseradish peroxidase (HRP) enzyme (i.e., baroreceptor) to alternatively catalyze phenolic alcohols. The biosensor displayed a significantly low limit of detection limit (LOD) of value 0.2 × 10-6 M towards 17ß-estradiol. The Mechaelis-Menten constant (Km) with the magnitude of 0.64 × 10-6 M was obtained; this indicates an outstanding affinity of the biosensing films towards 17ß-estradiol. Subsequently, the developed biosensor was able to accurately and efficiently measure successive concentrations of 17ß-estradiol from 0.2 × 10 to 4 × 10-6 M. The fabricated biosensor showed good selectivity towards 17ß-estradiol compared to the other estrogenic endocrine-disrupting compounds such as estrone (E1), ethnylstradiol (EE2), and estriol (E3). The biosensor was capable of detecting 17ß-estradiol in spiked tap water samples with good recoveries, thus affirming its potential to be applied for real electro-analysis of 17ß-estradiol in treated wastewater.

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Complex composite films based on polyaniline (PANI) doped hydrochloric acid (HCl) incorporated with aluminum nitrate (Al(NO3)3) on Au-layer were designed and synthesized as a surface plasmon resonance (SPR) sensing device. The physicochemical properties of (PANI-HCl)/Al(NO3)3 complex composite films were studied for various Al(NO3)3 concentrations (0, 2, 4, 8, 16, and 32 wt.%). The refractive index of the (PANI-HCl)/Al(NO3)3 complex composite films increased continuously as Al(NO3)3 concentrations increased. The electrical conductivity values increased from 5.10 µS/cm to 10.00 µS/cm as Al(NO3)3 concentration increased to 32 wt.%. The sensitivity of the SPR sensing device was investigated using a theoretical approach and experimental measurements. The theoretical system of SPR measurement confirmed that increasing Al(NO3)3 in (PANI-HCl)/Al(NO3)3 complex composite films enhanced the sensitivity from about 114.5 [Deg/RIU] for Au-layer to 159.0 [Deg/RIU] for Au-((PANI-HCl)/Al(NO3)3 (32 wt.%)). In addition, the signal-to-noise ratio for Au-layer was 3.95, which increased after coating by (PANI-HCl)/Al(NO3)3 (32 wt.%) complex composite layer to 8.82. Finally, we conclude that coating Au-layer by (PANI-HCl)/Al(NO3)3 complex composite films enhances the sensitivity of the SPR sensing device.

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Environmental pollution with cadmium (Cd) is a major concern worldwide, with prolonged exposure to this toxic heavy metal causing serious health problems, such as kidney damage, cancer, or cardiovascular diseases, only to mention a few. Herein, a gold-coated reflection-type fiber optic--surface plasmon resonance (Au-coated FO-SPR) sensor is manufactured and functionalized with (i) bovine serum albumin (BSA), (ii) chitosan, and (iii) polyaniline (PANI), respectively, for the sensitive detection of cadmium ions (Cd2+) in water. Then, the three sensor functionalization strategies are evaluated and compared one at a time. Out of these strategies, the BSA-functionalized FO-SPR sensor is found to be highly sensitive, exhibiting a limit of detection (LOD) for Cd2+ detection at nM level. Moreover, the presence of Cd2+ on the FO-SPR sensor surface was confirmed by the X-ray photoelectron spectroscopy (XPS) technique and also quantified consecutively for all the above-mentioned functionalization strategies. Hence, the BSA-functionalized FO-SPR sensor is sensitive, provides a rapid detection time, and is cheap and portable, with potential applicability for monitoring trace-level amounts of Cd within environmental or potable water.

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This paper provides an overview of the application of conducting polymers (CPs) used in the design of tactile sensors. While conducting polymers can be used as a base in a variety of forms, such as films, particles, matrices, and fillers, the CPs generally remain the same. This paper, first, discusses the chemical and physical properties of conducting polymers. Next, it discusses how these polymers might be involved in the conversion of mechanical effects (such as pressure, force, tension, mass, displacement, deformation, torque, crack, creep, and others) into a change in electrical resistance through a charge transfer mechanism for tactile sensing. Polypyrrole, polyaniline, poly(3,4-ethylenedioxythiophene), polydimethylsiloxane, and polyacetylene, as well as application examples of conducting polymers in tactile sensors, are overviewed. Attention is paid to the additives used in tactile sensor development, together with conducting polymers. There is a long list of additives and composites, used for different purposes, namely: cotton, polyurethane, PDMS, fabric, Ecoflex, Velostat, MXenes, and different forms of carbon such as graphene, MWCNT, etc. Some design aspects of the tactile sensor are highlighted. The charge transfer and operation principles of tactile sensors are discussed. Finally, some methods which have been applied for the design of sensors based on conductive polymers, are reviewed and discussed.

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Symmetrical supercapacitor is prepared with polyaniline (PANI) deposited on Au-coated porous nylon substrate as the electrodes and polyvinyl alcohol (PVA) /H2SO4 as the electrolyte. Successive abnormal phenomena occur that nylon becomes from opaque to transparent followed by PANI turning from green into black, also, the corresponding supercapacitor performance presents a significant improvement. The amide bond in the nylon is hydrolyzed by H2SO4 to form monomer, which is then esterified to produce aromatic ester by PVA combined with H2SO4 as the catalyst. The aromatic ester is transparent, thus leading to the nylon transparency. Moreover, the N-containing functional group in the nylon would be grafted to PANI by using the current collector Au as the catalyst, thus resulting in in-situ PANI nitridation with color turning from green into black. The in-situ PANI nitridation can be modulated (i) by controlling the nylon transparency, which can be modulated by the experimental temperature and humidity and (ii) by changing the current collector material, which serves as the catalyst to motivate the in-situ PANI nitridation. Due to high conductivity and high reversible redox reactivity of the nitrided PANI, the corresponding supercapacitor displays high specific capacitance (649.5 mF cm-2 at 0.5 mA cm-2), long cycling life (93.9% of the retained capacity after 6500 cycles), both high energy density and high power density (65.0 µW h cm-2 at 0.3 mW cm-2; 41.9 µW h cm-2 at 30.0 mW cm-2) and good flexibility.

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This study aims to design a new nanocomposite as a supporting material for wiring the enzyme to develop a bioanode in the enzymatic biofuel cell (EBFC). In this work, polyaniline-based nanocomposite was synthesized by in situ polymerization of aniline monomer. The zeta potential study of the nanofillers was carried out, which reveals the interaction between the nanofillers. The synthesized nanocomposite (MWCNT/ZnS/AgNWs/PANI) was characterized by analytical techniques, such as Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction spectroscopy (XRD). Furthermore, the surface morphology and the in-depth information of the synthesized nanocomposite were displayed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), respectively. In addition, the as-synthesized nanocomposite and the designed bioanode underwent the electrochemical assessment using different electrochemical techniques such as cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and linear sweep voltammetry (LSV) for evaluating the electrochemical behavior of the fabricated anodes. The electrochemically regulated bioanode (MWCNT/ZnS/AgNWs/PANI/Frt/GOx) obtained an open-circuit voltage of 0.55 V and produced a maximal current density of 7.6 mA cm-2 at a glucose concentration of 50 mM prepared in phosphate buffer solution (PBS) (pH 7.0) as a supporting electrolyte at a scan rate of 100 mV s-1.

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Exploiting efficient strategies for the selective separation and extraction of valuable metals from e-waste is in urgent demand to offset the ever-increasing depletion of metal resources, satisfy the sustainable supply of metal resources, and reduce the environmental impact from toxic metals. Herein, an asymmetric electrochemical system, constructed by polyaniline (PANI) nanofibers grown on carbon cloth (CC) and CC as the respective counter and working electrodes, is presented for the simultaneous and selective extraction of gold and copper from e-waste leachate solution. Harnessing the established CC/PANI//CC system, CC/PANI as the anode electrode is capable of selectively and rapidly extracting gold with high efficiency, accompanied by excellent reusability. Meanwhile, cathodic CC electrode is found to achieve almost 100% recovery of copper at a voltage of -1.2 V. Furthermore, the feasibility of the proposed asymmetric electrochemical system is further exemplified in waste central processing unit (CPU) leaching solution, enabling to recover simultaneously gold and copper with high purity. This work will provide meaningful guidance for simultaneous separation and recovery of multiple valuable metals from real e-waste.

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Herein, we present new approaches for developing sulfonated polyether ether ketone (SPEEK) and polyaniline-based (PANI) actuator formed by film-casting and chemical reduction of Pt electrodes. We have thoroughly studied the synthesis of SPEEK and characterized it by different analytical techniques. The ion-exchange capacity (IEC) and proton conductivity of SPEEK-PANI polymer membrane were calculated to be 1.98 mmol g-1 and 1.97 × 10-3 S cm-1, respectively. To develop an IPMC actuator, SPEEK was combined with PANI through in-situ polymerization method. SEM and XRD were used to check the morphology of the given SPEEK-PANI-Pt membrane. In addition, FT-IR and EDX techniques confirmed the molecular structure and chemical conformation of SPEEK-PANI polymer membrane. Pt electrode layers homogeneously dispersed on the IPMC membrane surface, which was demonstrated by smooth SEM micrographs. The actuation functioning, including the high bending deflection, proton conductivity, current density and IEC of IPMC actuator based on SPEEK-PANI-Pt, was obtained owing to its strong electrochemical and electromechanical characteristics. Synergistic combinations of SPEEK and PANI produced membrane that are flexible, mechanically strong and robust. The developed materials have immense capability as actuators for various applications including in biomimetics and robotics.

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Recent studies of lithium-sulfur (Li-S) batteries have identified that a modified separator plays a critical role in challenging the capacity fading and shuttle effect of lithium polysulfides (LiPSs). Herein, we report a polyaniline-encapsulated hollow Co-Fe Prussian blue analogue (CFP@PANI) for separator modification. The open frame-like hollow CFP was synthesized via oriented attachment (OA). To improve the catalytic effect and electrical conductivity, PANI was coated on the synthesized CFP. The resulting CFP@PANI was applied on the conventional polypropylene (PP) separator (CFP@PANI-PP) with vacuum filtration. With a ketjen black/sulfur (KB/S) cathode with 66% of the sulfur load, the CFP@PANI-PP exhibited an initial capacity of 723.1 mAh g-1 at a current density of 1 A g-1. Furthermore, the CFP@PANI-PP showed stable cycling performance with 83.5% capacity retention after 100 cycles at 1 A g-1. During the 100 cycles, each cycle maintained high coulombic efficiency above 99.5%, which indicates that the CFP@PANI-PP could inhibit LiPS migration to the anode side without a Li+ transport disturbance across the separator. Overall, the CFP@PANI-PP efficiently suppressed LiPSs, resulting in enhanced electrochemical performance. The current study provides useful insight into designing a nanostructure for separator modification of Li-S batteries.

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Polyaniline (PANI) was synthesized using oxidative polymerization in a mixture of water with pyrrolidinium hydrogen sulfate [Pyrr][HSO4], which is a protic ionic liquid PIL. The obtained PANI (PANI/PIL) was compared with conventional PANI (PANI/HCl and PANI/HSO4) in terms of their morphological, structural, and storage properties. The results demonstrate that the addition of this PIL to a polymerization medium leads to a fiber-like morphology, instead of a spherical-like morphology, of PANI/HSO4 or an agglomerated morphology of PANI/HCl. In addition, PAN/PIL exhibits an improvement of the charge transfer kinetic and storage capability in H2SO4 1 mol·L-1, compared to PANI/HCl. The combination of PANI/PIL and graphene oxide (GO), on the other hand, was investigated by optimizing the PANI/GO weight ratio to achieve the nanocomposite material with the best performance. Our results indicate that the PANI/PIL/GO containing 16 wt% of GO material exhibits a high performance and stability (223 F·g-1 at 10 A·g-1 in H2SO4 1 mol·L-1, 4.9 Wh·Kg-1, and 3700 W·Kg-1 @ 10 A·g-1). The obtained results highlight the beneficial role of PIL in building PANI and PANI/GO nanocomposites with excellent performances for supercapacitor applications.

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In this work, we report results on the fabrication and characterization of a surface plasmon resonance (SPR) pH sensor using platinum (Pt) and polyaniline (PANI) layers successively coated over an unclad core of an optical fiber (FO). The plasmonic thin Pt layer was deposited using a magnetron sputtering technique, while the pH-sensitive PANI layer was synthesized using an electroless polymerization method. Moreover, the formation of PANI film was confirmed by X-ray photoelectron spectroscopy (XPS) technique and its surface morphology was investigated using scanning electron microscopy (SEM). It was found that the PANI/Pt-coated FO-SPR pH sensor exhibits a fast and linear response in either acid or alkali solutions (pH operational range: 1 to 14). The proposed FO-SPR sensor could be used for biomedical applications, environmental monitoring or any remote, real-time on-site measurements.

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Sensing targeted tumor markers with high sensitivity provides vital information for the fast diagnosis and treatment of cancer patients. A vascular endothelial growth factor (VEGF165) have recently emerged as a promising biomarker of tumor cells. The electrochemical aptasensor is a promising tool for detecting VEGF165 because of its advantages such as a low cost and quantitative analysis. To produce a sensitive and stable sensor electrode, nanocomposites based on polyaniline (PANI) and carbon nanotube (CNT) have potential, as they provide for easy fabrication, simple synthesis, have a large surface area, and are suitable in biological environments. Here, a label-free electrochemical aptasensor based on nanocomposites of CNT and PANI was prepared for detecting VEGF165 as a tumor marker. The nanocomposite was assembled with immobilized VEGF165 aptamer as a highly sensitive VEGF165 sensor. It exhibited stable and wide linear detection ranges from 0.5 pg/mL to 1 µg/mL, with a limit of detection of 0.4 pg/mL because of the complementary effect of PANI/CNT. The fabricated aptasensor also exhibited good stability in biological conditions, selectivity, and reproducibility after several measurement times after the dissociation process. Thus, it could be applied for the non-invasive determination of VEGF, in biological fluid diagnosis kits, or in an aptamer-based biosensor platform in the near future.

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In-situ iodine (I2)-doped atmospheric pressure (AP) plasma polymerization is proposed, based on a newly designed AP plasma reactor with a single wire electrode that enables low-voltage-driven plasma polymerization. The proposed AP plasma reactor can proceed plasma polymerization at low voltage levels, thereby enabling an effective in-situ I2 doping process by maintaining a stable glow discharge state even if the applied voltage increases due to the use of a discharge gas containing a large amount of monomer vapors and doping materials. The results of field-emission scanning electron microscopy (FE-SEM) and Fourier transformation infrared spectroscopy (FT-IR) show that the polyaniline (PANI) films are successfully deposited on the silicon (Si) substrates, and that the crosslinking pattern of the synthesized nanoparticles is predominantly vertically aligned. In addition, the in-situ I2-doped PANI film fabricated by the proposed AP plasma reactor exhibits excellent electrical resistance without electrical aging behavior. The developed AP plasma reactor proposed in this study is more advantageous for the polymerization and in-situ I2 doping of conductive polymer films than the existing AP plasma reactor with a dielectric barrier.