Conducting polymers (CPs) have emerged as promising materials for gas sensors due to their organic nature coupled with unique and versatile optical, electrical, chemical, and electrochemical properties. This review provides a comprehensive overview of the latest developments in conducting polymer-based gas sensors. First, the fundamental gas sensing mechanisms in CPs-based sensors are elucidated, covering diverse transduction modes including electrochemical, chemiresistive, optical, piezoelectric, and field-effect transistor-based sensing. Next, the various types of conducting polymers employed in gas sensors, such as polypyrrole, polyaniline, polythiophene, and their composites are introduced, with emphasis on their synthesis methods, structural characteristics, and gas sensing response properties. Finally, the wide range of applications of these sensors is discussed, spanning industrial process control, environmental monitoring, food safety, biomedical diagnosis, and other fields, as well as existing issues such as long-term stability and humidity interference, and a summary of the biocompatibility and regulatory standards of these conductive polymers is provided. By integrating insights from sensing mechanisms, materials, and applications, this review offers a holistic understanding of CPs-based gas sensors. It also highlights future research directions, including device miniaturization, AI-assisted gas identification, multifunctional integrated sensing systems, wearable and flexible sensor platforms, and enhanced sensitivity, selectivity, and on-site detection capabilities.

In this paper, piperazine-grafted reduced graphene oxide (NH-rGO) was synthesized via a simple and green two-step procedure: (i) opening of the resulting epoxides of graphene oxide (GO) with piperazine (NH) through nucleophilic substitution; (ii) reduction of GO with ascorbic acid. Its structure and morphology were characterized by scanning electron microscopy and x-ray photoelectron spectroscopy. The NH-rGO modified glassy carbon electrode was explored as an electrochemical sensor for the determination of Hg(II) using a differential pulse anodic stripping voltammetry technique. Hg(II) can be efficiently accumulated and deposited on the surface of a modified electrode by strong coordination chemical bonds formed between Hg(II) and NH. And then the anodic stripping current can be significantly enhanced by rGO with the merits of large specific surface area and high conductivity, which served as a signal amplifier, finally realizing the highly sensitive determination of Hg(II). The experimental parameters including the pH value of the acetate buffer, deposition potential and deposition time were optimized. Under optimal conditions, the developed sensor exhibited a wide linear range from 0.4–12 000 nM with a low limit of detection of 0.2 nM, which is well below the guideline value in drinking water set by the WHO. Moreover, the practical application of this method was confirmed by an assay of Hg(II) in tap water samples with acceptable results.