The alarming rise of indoor pollution and the need to combat the associated negative effects have promoted increasing attention in modernizing the chemical sensing technologies by newly designed materials with rich and tunable functionalities at atomic or molecular levels. With the appealing physical, chemical, optical, and electronic properties for various potential applications, the state-of-art gas-sensing nanomaterials and their future perspectives are well-documented and summarized in this paper. Specifically, the key performance attributes are addressed in detail such as the sensitivity, selectivity, reversibility, operating temperature, response time, and detection limit. As such, this review provides both critical insights in exploring and understanding various gas sensing nanomaterials and points out limitations and opportunities for further developments, such as morphology control, doping and surface alteration, atomic-scale characterization, and applications in different fields. Finally, the challenges and outlooks are discussed on the basis of the current developments.

Functional gas sensing nanomaterials: A panoramic view

Here we present, a useful ammonia (NH3) gas sensor based on polyaniline (PANI) film as an active sensing layer. The PANI films were successfully deposited on a polyethylene terephthalate (PET) flexible substrate by a simple in-situ polymerization technique. Ammonia (NH3) gas-sensing properties of the films prepared at optimum conditions were examined at room temperature in the range of 5–1000 ppm. The room temperature functioning of the sensor is critical, which facilitates low-power operation and also enhances the life time of a sensor. The observed variation in resistance of PANI film corresponding to 1000 ppm and 200 ppm of NH3 exposure, is approximately 520 and 110 times of that observed for ∼5 ppm of NH3. Furthermore, good reproducibility and long-term stability were also observed over a concentration range from 5 to 1000 ppm. Moreover the sensor is mechanically robust and can be bent sharply without damage, demonstrating excellent mechanical stability and exhibiting no lack in performance even after several bending cycles. These results indicate that the PANI films on flexible substrates are promising for portable on-site detection.

Flexible room temperature ammonia sensor based on polyaniline

Since the first suggestion, during the 1950s, that high-surface-area metal oxides could be used as conductometric gas sensors enormous efforts have been made to enhance both the selectivity and the sensitivity of such devices, and to reduce their operational power requirements. This development has involved the exploration of response mechanisms, the selection of the most appropriate oxide compositions, the fabrication of two-phase ‘hetero-structures’, the addition of metallic catalyst particles and the optimisation of the manner in which the materials are presented to the gas—the structure and the nanostructure of the sensing elements. Far more of the scientific literature has been devoted to seeking such improvements in metal oxide gas sensors than has been directed at all other solid-state gas sensors together. Recent progress in the research and development of metal oxide gas sensor technology is surveyed in this invited review. The advances that have been made are quite spectacular and the results of individual pieces of work are drawn together here so that trends can be seen. Emerging features include: the significance of n-type/p-type switching, the enhancement of sensing performance of materials through the incorporation of secondary components and the advantages of interrogating sensors with alternating current rather than direct current.

https://iopscience.iop.org/article/10.1088/1361-6501/aa7443/pdf

Progress in the development of semiconducting metal oxide gas sensors: a review

Recently, there is an increasing interest in ammonia sensing and detection for a wide range of applications, including food, automotive, chemical, environmental, and medical sectors. A major challenge is to obtain selective, sensitive and environmentally stable sensing polymer/chemical materials that can meet the stringent performance requirements of these application areas. Among various polymer-based sensing materials, polyaniline has emerged as a preferred choice owing to its cost-effectiveness, facile preparation steps, and superior sensing performance towards ammonia. In this review, advances in polyaniline based ammonia detection sensors are summarized, with a special focus on progresses in polyaniline modification techniques to achieve enhanced sensing performance. These techniques utilize interfacial and high dilution syntheses, multifunctional dopants, template synthesis, self-oxidizing template synthesis, etc. , methods. Most up-to-date developments in combining polyaniline with other ammonia sensing materials, including polyaniline nanocomposites with metal oxides, graphene, carbon nanotubes and other carbon nanomaterials, are included. These novel nanocomposites have special capabilities of forming p - n nanojunctions or electron interphase interactions for superior detection sensitivity and selectivity. In addition, existing challenges toward understanding, reproducing, and optimizing the design of polyaniline based ammonia sensors are discussed.

A review on advances in application of polyaniline for ammonia detection

A resistive-type flexible ammonia (NH3) sensor was proposed and developed in this work, which was prepared by depositing polyaniline-cerium dioxide (PANI-CeO2) nanocomposite thin film on flexible polyimide (PI) substrate through in-situ self-assembly method. The effect of CeO2 nanoparticles on the polymerization of aniline was studied by comparing the morphological, structural and chemical features of the pure PANI and PANI-CeO2 nanocomposite, and the dynamic polymerization processes were also recorded and investigated. In this process, an interesting phenomenon was found that the protonation and oxidation degrees of PANI in PANI-CeO2 nanocomposite were improved significantly according to the XPS spectra analysis, which should be ascribed to the synergetic oxidation of CeO2 nanoparticles and ammonium persulfate (APS). Meanwhile, the NH3-sensing performances of the pure PANI and PANI-CeO2 film sensors were evaluated at room temperature (∼25 °C), which showed that the PANI-CeO2 film sensor possessed enhanced response, reduced recovery time, perfect response-concentration linearity, good reproducibility, splendid selectivity, remarkable long-term stability, ultra-low detectable concentration (16 ppb) and theoretical detection limit (0.274 ppb), and outstanding flexibility without significant response decrease after 500 bending/extending cycles. It was speculated that the excellent sensing performances should probably benefit from the gas-sensing enhancement effect of p-n junction, the improved protonation degree and modified morphology of PANI by the addiction of CeO2 nanoparticles. And, the high flexibility might originate from the flexible structure of PANI chains, and the good adhesion and nano-mechanical performance of PANI-CeO2 film. Besides, the effect of relative humidity on the sensing properties of PANI-CeO2 film sensor was also discussed and analyzed. Therefore, the proposed high-performance flexible PANI-CeO2 thin film sensor holds great promise for application into hand-held or wearable electronic devices for trace-level NH3 detection at room temperature.

A high-performance flexible gas sensor based on self-assembled PANI-CeO2 nanocomposite thin film for trace-level NH3 detection at room temperature

We prepared a heterostructure hybrid of PANI and SnO 2 by a rapid and facile in situ chemical oxidation polymerization under very low monomer concentration, and the hybrid was loaded on a flexible PET thin film to structure a smart NH 3 sensor. The structure, morphology and thermal stability of the hybrid were characterized by various analysis methods. Compared with those reported in literatures, the hybrid-based sensor not only has high sensitivity, good selectivity and wide linear response to NH 3 at room temperature of 21 °C but also has flexible, structure simple and wearable performance. The room temperature operating of the sensor is particularly interesting, which leads to low-power consumption, environmental safety and long life times of the sensing materials. The improvement of sensing properties is attributed to the complementary and synergistic effect between SnO 2 and PANI, and formation of p−n heterojunction at the interface in hybrid.

Polyaniline@SnO2 heterojunction loading on flexible PET thin film for detection of NH3 at room temperature

A Cu2O/BiVO4 p-n heterojunction based photoanode in photoelectrochemical (PEC) water splitting is fabricated by a two-step electrodeposition method on an FTO substrate followed by annealing treatment. The structures and properties of the samples are characterized by XRD, FESEM, HRTEM, XPS and UV-visible spectra. The photoelectrochemical activity of the photoanode in water oxidation has been investigated and measured in a three electrode quartz cell system; the obtained maximum photocurrent density of 1.72 mA cm-2 at 1.23 V vs. RHE is 4.5 times higher than that of pristine BiVO4 thin films (∼0.38 mA cm-2). The heterojunction based photoanode also exhibits a tremendous cathodic shift of the onset potential (∼420 mV) and enhancement in the IPCE value by more than 4-fold. The enhanced photoelectrochemical properties of the Cu2O/BiVO4 photoelectrode are attributed to the efficient separation of the photoexcited electron-hole pairs caused by the inner electronic field (IEF) of the p-n heterojunction.

Two-step electrodeposition to fabricate the p–n heterojunction of a Cu2O/BiVO4 photoanode for the enhancement of photoelectrochemical water splitting

Hybrids of reduced graphene oxide (rGO)–MoO3 nanorods were synthesized successfully by a facile in situ solution growth method under a relatively low temperature of 150 °C for 1 h. The structure and properties of the hybrids have been characterized by XRD, SEM, TEM, Raman, PL and XPS analysis. The sensing performance of pure MoO3 and rGO–MoO3 hybrids to H2S were examined, the results indicate that the hybrids exhibit higher response and lower operating temperature compared with the pure MoO3 nanorods, especially, the 2.5 wt% rGO–MoO3 hybrid exhibits the highest sensitivity and the fastest response to H2S, which makes them promising candidates in the field of gas sensors for detection of H2S gas. The sensing mechanism for MoO3 to H2S which is enhanced is also discussed in detail from rGO action in the hybrid and formation of a hetero-junction at the interface of the hybrid.

Rapid synthesis of rGO–MoO3 hybrids and mechanism of enhancing sensing performance to H2S

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Polyaniline@SnO2 heterojunction loading on flexible PET thin film for detection of NH3 at room temperature

Two-step electrodeposition to fabricate the p–n heterojunction of a Cu2O/BiVO4 photoanode for the enhancement of photoelectrochemical water splitting

Rapid synthesis of rGO–MoO3 hybrids and mechanism of enhancing sensing performance to H2S