RESUMEN
Conductive graphene polymer composites are considered promising functional materials in gas detection, strain detection, metal corrosion prevention, and electromagnetic wave absorption, owing to their good flexibility, lightweight, and adjustable conductivity. The internal defects or external damages of composite films will seriously affect the electrical and functional properties of the materials. Based on the conductive network inside the conductive polymer film and the self-inductance to ultrasonic wave, the defect self-monitoring system of the conductive polymer film is designed and optimized in this work. The self-damage detection system is composed of an electrode array, excitation source, resistance signal acquisition and processing circuit, and damage display. Aiming at different scenarios, the improved interdigital structure transducer for sensors and damage detection device for coating film with a large area are presented and optimized respectively. Meanwhile, the damage location algorithm based on time difference measurement and kernel density estimation algorithm is also optimized. The multiple damage detection is realized by a device with a 4 × 8 electrode array, and the relative error of damage area with 1 mm × 1 mm is less than 5%, and the lower detection limits of damage size are 0.3 mm × 0.3 mm.
RESUMEN
Recently, as a two-dimensional (2D) material, black phosphorous (BP) has attracted more and more attention. However, few efforts have been made to investigate the BP/polyaniline (PANI) nanocomposite for ammonia (NH3) gas sensors. In this work, the BP/PANI nanocomposite as a novel sensing material for NH3 detection, has been synthesized via in situ chemical oxidative polymerization, which is then fabricated onto the interdigitated transducer (IDTs). The electrical properties of the BP/PANI thin film are studied in a large detection range from 1 to 4000 ppm, such as conduction mechanism, response, reproducibility, and selectivity. The experimental result indicates that the BP/PANI sensor shows higher sensitivity and larger detection range than that of PANI. The BP added into PANI, that may enlarge the specific surface area, obtain the special trough structure for gas channels, and form the p-π conjugation system and p-p isotype heterojunctions, which are beneficial to increase the response of BP/PANI to NH3 sensing. Meanwhile, in order to support the discussion result, the structure and morphology of the BP/PANI are respectively measured by Fourier transform infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-vis), transmission electron microscopy (TEM), and field emissions scanning electron microscopy (SEM). Moreover, the sensor shows good reproducibility, and fast response and recovery behavior, on NH3 sensing. In addition, this route may offer the advantages of an NH3 sensor, which are of simple structure, low cost, easy to assemble, and operate at room temperature.
RESUMEN
Designing sensing materials with novel morphologies and compositions is eminently challenging to achieve high-performance gas sensor devices. Herein, an in situ oxidative polymerization approach is developed to construct three-dimensional (3D) hollow quasi-graphite capsules/polyaniline (GCs/PANI) hierarchical hybrids by decorating protonated PANI on the surface of GCs; as a result, an immensely active and sensitive material was developed for sensing ammonia gas at room temperature. Moreover, the GCs possessed a capsule-like hollow/open structure with partially graphitized walls, and PANI nanospheres were uniformly decorated on the GC surfaces. Furthermore, the inflexible and rigid 3D ordered chemistry of these materials provides the resulting hybrids with a large interfacial surface area, which not only allows for rapid adsorption and charge transfer but also provides the necessary structural stability. The 3D hollow GCs/PANI hybrids exhibit excellent performance; the GCs/PANI-3 hybrid is highly sensitive (with a response value of 1.30) toward 10 ppm NH3 gas and has short response and recovery times of 34 and 42 s, respectively. The GCs/PANI-3 hybrid also demonstrates a good selectivity, repeatability, and long-term stability, which are attributed to the substantial synergistic effect of the GCs and PANI. The design of such a unique 3D ordered framework provides a promising pathway to achieve room-temperature gas sensors for commercial applications.
Asunto(s)
Amoníaco/análisis , Compuestos de Anilina/química , Técnicas de Química Analítica/instrumentación , Grafito/química , Temperatura , Cápsulas , HumedadRESUMEN
In this paper, a novel graphene oxide (GO)/polyaniline (PANI) sandwich-like nanocomposite has been synthesized by in-situ chemical oxidative polymerization. The GO/PANI is then fabricated onto the interdigitated transducers as sensor for humidity detection. The electrical properties of the thin films are investigated in various relative humidity (RH), including conduction mechanism, sensitivity, reproducibility and humidity hysteresis. The conduction mechanism of the GO/PANI for humidity response is discussed in detail, and the total resistance of GO/PANI is mainly depending on the bulk resistance of PANI. At the lower (60%) RH, the proton hopping transfer plays a very important role for the proton exchange mechanism of GO/PANI thin film. At the higher RH, ionic conduction is not only main conduction process, but also with the proton hopping partially exists for the proton exchange mechanism. Besides, the humidity sensitivity of the thin films enhances with increasing the mass ratio of GO (0, 5, and 50 mg) to PANI due to its larger surface area, hydrophilic functional groups and synergistic effect of π-π* conjugation system, which is also supported by adsorption of QCM humidity response. Meanwhile, the morphology and structure of the thin films are analyzed by fourier transform infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-vis), scanning electron microscopy (SEM) and transmission electron microscope (TEM), respectively.
RESUMEN
We investigate the effect of water adsorption on the electrical properties of graphene oxide (GO) films using the direct current (DC) measurement and alternating current (AC) complex impedance spectroscopy. GO suspension synthesized by a modified Hummer's method is deposited on Au interdigitated electrodes. The strong electrical interaction of water molecules with GO films was observed through electrical characterizations. The DC measurement results show that the electrical properties of GO films are humidity- and applied voltage amplitude-dependent. The AC complex impedance spectroscopy method is used to analyze the mechanism of electrical interaction between water molecules and GO films in detail. At low humidity, GO films exhibit poor conductivity and can be seen as an insulator. However, at high humidity, the conductivity of GO films increases due to the enhancement of ion conduction. Our systematic research on this effect provides the fundamental supports for the development of graphene devices originating from solution-processed graphene oxide.