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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.

The development of sensitive and selective methods for detecting pesticide residues has become paramount for ensuring food safety. In this work, a high-performance molecularly imprinted electrochemical sensor based on the composite of Cu-BTC- and FeCo-ZIF-derived N-doped carbon (FeCo@NC), synthesized by pyrolysis and electrodeposition, was developed for Benomyl (BN) detection. The materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). In this sensing system, the Cu-BTC/FeCo@NC composite used as the electrode substrate displayed a large specific surface area, high electronic conductivity, and rich active catalytic sites, demonstrating excellent electrocatalytic ability toward BN oxidation. Meanwhile, Cu-BTC, with its abundant surface functional groups, facilitated strong hydrogen bonding interactions with the imprinted template molecule of 3,4-ethylenedioxythiophene (EDOT), promoting the formation of a uniform molecularly imprinted membrane on the substrate material surface. The introduced MIP-PEDOT could enhance the selective recognition and enrichment of the target BN, leading to an amplified detection signal. Thanks to the synergistic effects between Cu-BTC/FeCo@NC and MIP-PEDOT, the proposed sensor achieved a low detection limit of 1.67 nM. Furthermore, the fabricated sensor exhibited high selectivity, reproducibility, and interference resistance in detecting BN. The method has been successfully applied to the determination of BN in vegetable and fruit samples, indicating its potential for use in practical applications.

Chemiresistive breath humidity sensors (CRBHSs) have emerged as a promising technology for non-invasive health monitoring, offering high sensitivity, a simple device architecture, strong miniaturization potential, and low power consumption. This review summarizes recent progress in CRBHSs from three core perspectives: sensing mechanisms, material systems, and device applications. First, we outline the fundamental sensing principles, emphasizing the Grotthuss proton-hopping mechanism and the resistance modulation associated with water adsorption/desorption. Next, we discuss structural engineering strategies for zero-dimensional (0D), one-dimensional (1D), two-dimensional (2D), and three-dimensional (3D) sensing materials, highlighting how dimensional design can balance water uptake, charge transport, mechanical compliance, and wearability. Finally, we review representative applications ranging from healthcare diagnostics and respiratory monitoring to emotion- and behavior-related assessment. Overall, this review integrates the mechanism–material–application relationship to provide a cohesive understanding of CRBHSs; identifies key challenges such as environmental stability and anti-interference performance; and outlines future directions, including performance optimization, flexible/wearable integration, and intelligent sensor systems.

A novel molecularly imprinted sensor was developed for the voltammetric determination of adrenaline (AD). MXene/carbon nanohorn (MXene/CNH) composite with good electric conductivity and enormous accessible active sites was firstly introduced as catalytic substrate. Subsequently, molecularly imprinted polymer (MIP) film was fabricated in mixed solutions containing hydroxymethyl-3,4-ethylenedioxythiophene (functional monomer) and AD (template) through electro-polymerization process. A molecularly imprinted sensor was formed after removing the template. The morphology and elemental composition of the prepared composites were studied by scanning electron microscopy and X-ray photoelectron spectroscopy. Cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS) were used to investigate the electrochemical performance of the molecularly imprinted sensors. Under optimized conditions, the designed sensor displays a wide linear range from 1.0 nM to 60.0 μM and a low limit of detection of 0.3 nM. The developed sensor also presents good selectivity, reproducibility and long-term stability, and satisfactory feasibility in practical sample analysis. Graphical abstract MXene/carbon nanohorns decorated with conductive molecularly imprinted poly(hydroxymethyl-3,4-ethylenedioxythiophene) was proposed for highly sensitive and selective detection of adrenaline.

In this work, a two-dimensional leaf-like framework-L embedded electrochemically reduced graphene oxide (ERGO@ZIF-L) was proposed as an outstanding electrode material for the sensitive electrochemical sensing of benomyl (BM). ZIF-L is surrounded by ERGO, which could effectively ensure the stability and dispersion of ZIF-L. With this unique combination, the prepared ERGO@ZIF-L displayed excellent synergistic characteristics with a large surface area, excellent conductivity, plentiful active sites, and high electrocatalytic properties, thus endowing it with high sensitivity for BM determination. The experimental parameters, such as solution pH, material volume, and accumulation time, were optimized. Under optimal conditions, the BM sensor showed a wide linear range (0.009–10.0 μM) and low-limit detection (3.0 nM). Moreover, the sensor displayed excellent stability, repeatability, and reproducibility, and good anti-interference capability. The method was successfully applied to detect BM in real-world samples.

Heavy metal pollution has posed a serious threat to the ecological environment and human health. Thus, the development of accurate and effective methods for their detection is crucial. In this study, a novel electrochemical sensor was fabricated to detect Cu2+ and Hg2+, based on N-doped carbon nanotube-wrapped Ni nanoparticle (Ni@N-CNT) sensing material, which was derived from the pyrolysis of Ni2+ doped ZIF-8. For electrode material design, the packaging structure not only protected the encapsulated Ni nanoparticles from electrochemical corrosion in the acid electrolyte but also provided excellent electro-catalytic activity and electrical conductivity by controlling their size. Thanks to the overall performance of the Ni@N-CNT composite, the proposed sensor exhibited excellent analytical performance for Cu2+ and Hg2+ detection, with ultra-low detection limits of 33.3 ng⋅L−1 and 33.3 ng⋅L−1, respectively. The sensor also demonstrated good repeatability, reproducibility and selectivity. In addition, the method was successfully applied to the electrochemical analysis of Cu2+ and Hg2+ in actual Chinese cabbage samples with satisfactory recovery, confirming its practical applicability.

In this work, TiO2-MXene/poly (3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS) composite was utilized as an electrode material for the sensitive electrochemical detection of baicalein. The in-situ growth of TiO2 nanoparticles on the surface of MXene nanosheets can effectively prevent their aggregation, thus presenting a significantly large specific surface area and abundant active sites. However, the partial oxidation of MXene after calcination could reduce its conductivity. To address this issue, herein, PEDOT:PSS films were introduced to disperse the TiO2-MXene materials. The uniform and dense films of PEDOT:PSS not only improved the conductivity and dispersion of TiO2-MXene but also enhanced its stability and electrocatalytic activity. With the advantages of a composite material, TiO2-MXene/PEDOT:PSS as an electrode material demonstrated excellent electrochemical sensing ability for baicalein determination, with a wide linear response ranging from 0.007 to 10.0 μM and a lower limit of detection of 2.33 nM. Furthermore, the prepared sensor displayed good repeatability, reproducibility, stability and selectivity, and presented satisfactory results for the determination of baicalein in human urine sample analysis.

In this work, carbon nanohorn (CNH)–decorated multi-walled carbon nanotube (MWCNT) (CNH@MWCNT) composite was prepared and used to modify glass carbon electrode (GCE) as sensitive electrochemical sensor for niclosamide (NA) determination. Herein, the decoration of CNHs induces higher dispersibility for MWCNTs, and endows the composite with better conductivity, larger surface area, and higher catalytic activity, which leads to significantly enhanced electrochemical behavior toward NA oxidation. The parameters such as mass ratios of CNHs and MWCHTs, the amount of composite materials, the accumulation time, and the solution pH are systematically optimized. Under optimized conditions, the developed electrochemical sensor exhibits a low detection limit of 2.0 nM with a wide linear range of 7.0 nM–10.0 µM and high anti-interference ability. In addition, the sensor displays good stability, repeatability, and reproducibility. The feasibility of the assay was verified by testing NA in brown rice and rice field water samples.

There is clearly a need for the development of new classes of antimicrobials to fight against multidrug-resistant bacteria. Here, we designed and synthesized of three ruthenium polypyridyl complexes: [Ru(bpy) 2 (BTPIP)](ClO 4 ) 2 ( Ru(II)-1 ), [Ru(bpy) 2 (ETPIP)](ClO 4 ) 2 ( Ru(II)-2 ) and [Ru(bpy) 2 (CAPIP)](ClO 4 ) 2 ( Ru(II)-3 ) ( N - N  = bpy = 2,2′-bipyridine), their antimicrobial activities against S. aureus were assessed. The lead complexes of this set, Ru(II)-1 (MIC = 0.016 mg/mL), was tested against biofilm. We also investigated whether bacteria can easily develop resistance to Ru(II)-1 . The result demonstrated that S. aureus could not easily develop resistance to the ruthenium complexes. In addition, aimed to test whether ruthenium complexes treatment could increase the susceptibility of S. aureus to antibiotics, the synergism between Ru(II)-1 and common antibiotics against S. aureus were investigated using the checkerboard method. Interesting, Ru(II)-1 could increased the susceptibility of S. aureus to some aminoglycoside antibiotics(kanamycin and gentamicin). Finally, in vivo bacterial infection treatment studies were also conducted through murine skin infection model. These results confirmed ruthenium complexes have good antimicrobial activity in vitro and in vivo. Graphic abstract

In this paper, Pt/Pd-poly(3,4-ethylenedioxythiophene)/nitrogen doped graphene (Pt/Pd-PEDOT/NGE) nanocomposites with hierarchical structure were prepared via a one-pot method. In the first step, Pd-PEDOT composites with Pd nanoparticles scattered on the surface or embedded in coralloid PEDOT particles were obtained through the redox reaction between PdCl 4 2− and 3,4-ethylenedioxythiophene (EDOT) monomer. NGE was then added to improve the electrical conductivity and continuity of the nanocomposites. Finally, the added PtCl 6 2− as well as the residual PdCl 4 2− was reduced by ethanol through heating reflux. As a result, the Pt/Pd-PEDOT/NGE nanocomposites were obtained with Pt and Pd nanoparticles well-dispersed on the surfaces of PEDOT granules and NGE nanosheets. The obtained Pt/Pd-PEDOT/NGE nanocomposites were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive spectroscopy (EDS), x-ray diffraction (XRD), x-ray photoelectron spectroscopy (XPS), and Raman spectra. The electrochemical sensing performance of the Pt/Pd-PEDOT/NGE modified glassy carbon for caffeic acid (CA) was mainly studied by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Under optimized conditions, Pt/Pd-PEDOT/NGE showed superior electrochemical sensing performance for detecting CA with the linear relationship ranging from 0.008 μM to 46 μM and a detection limit of 2.7 nM (a signal to noise ratio of 3 ( S / N  = 3)). Moreover the nanocomposite also possesses high anti-interference capability and reproducibility. The real sample analysis of Pt/Pd-PEDOT/NGE was successfully carried out, implying the promising application of CA detection in food and beverages.