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Chemiresistive sensors integrated with functionalized conductive polymers have emerged as promising candidates for wearable applications, offering adequate protection against highly toxic and widely prevalent organophosphate compounds, due to their high sensitivity, room-temperature operation, and straightforward fabrication process. However, these chemiresistive sensors exhibit poor resistance to water vapor due to the intrinsic properties of these conducting polymers, likely leading to false sensor alarms. In this study, we engineered a series of water-vapor-resistant, yet organophosphate-sensitive, conducting polymers by electro-copolymerizing hexafluoroisopropanol (HFIP)-grafted 3,4-ethylenedioxythiophene (EDOT-HFIP) with EDOT comonomers bearing hydrophobic alkyl groups of varying lengths (ethyl, butyl, and hexyl). The typical results indicated that increasing the alkyl length and alkyl-bearing EDOT comonomer composition significantly enhanced the water resistance of the EDOT-HFIP copolymers and the copolymer-integrated chemiresistive sensor, but this improvement came at the unacceptable cost of compromising the organophosphate sensitivity. To address this issue, we developed a surface-driven phase-segregation strategy to enrich the alkyl chains on the surface while concentrating the HFIP groups beneath it by treating the silica substrates using oxygen plasma before polymer spin coating, thus decoupling and optimizing the two mutually competing characteristics. Finally, the chemiresistive sensor integrated with the EDOT-HFIP copolymer containing 10% hexyl-grafted EDOT comonomer exhibited an organophosphate (DMMP) resistive response 657 times higher than that to water vapor, and more than two times that of a PEDOT-HFIP sensor, while preserving the original specific sensitivity of the PEDOT-HFIP sensor. Furthermore, it demonstrated a markedly improved shelf storage stability, being directly exposed to air for 14 days without any special protection. We envision that this surface-driven phase-segregation strategy could offer a promising solution to the significant challenge of air moisture interference in highly sensitive polymer sensors, promoting their practical use in real-world applications.
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http://dx.doi.org/10.3390/polym17070979 | DOI Listing |
Chem Rec
September 2025
School of Physics and Mechanics, Wuhan University of Technology, Wuhan, 430070, Hubei, P. R. China.
The development of sensors for monitoring breath acetone, a key biomarker for ketosis in diabetes mellitus, represents a critical frontier in medical diagnostics, promising a painless alternative to invasive blood tests. This review provides a comprehensive and critical evaluation of the state-of-the-art in acetone gas sensing technologies, including chemiresistive, optical, electrochemical, conductometric, and microwave platforms. We focus specifically on recent breakthroughs driven by advanced materials, analyzing how novel nanostructures from two-dimensional (2D) materials such as MXenes to porous metal-organic frameworks (MOFs) are engineered to push performance to clinically relevant parts-per-billion (ppb) sensitivity.
View Article and Find Full Text PDFACS Sens
September 2025
School of Chemical Engineering, Zhengzhou University, Zhengzhou, 450001, China.
Chemiresistive gas sensors have emerged as a promising technology for gas detection, due to their real-time response, low costs, high sensitivity, excellent stability, and facile fabrication. However, the full realization of their potential is currently constrained by the scarcity of sensing materials capable of delivering high selectivity and ultrafast response. In this study, we prepared a three-dimensional inverse opal macroporous SnO doped with NiO (3DIO NiO-SnO).
View Article and Find Full Text PDFSmall Methods
August 2025
School of Materials Science and Engineering, Jiangsu Key Laboratory for Advanced Metallic Materials, Southeast University, Nanjing, 211189, China.
Constructing transition metal dichalcogenides/oxides (TMDs/TMOs) heterostructures is an effective strategy to enhance their functional properties through band coupling and carrier migration. Furthermore, introducing a mesoporous architecture into TMDs/TMOs can significantly improve their porosity and specific surface area, thereby boosting their performance in chemical sensing, energy storage/conversion, and catalysis. However, it remains a significant challenge to realize a direct and facile synthesis of mesoporous TMDs/TMOs (mTMDs/TMOs) heterostructures with tunable compositions and abundant heterogeneous interfaces.
View Article and Find Full Text PDFNanoscale
August 2025
Hybrid Porous Materials Lab, Department of Chemistry, Indian Institute of Technology Jammu, Jammu & Kashmir, 181221, India.
Among various pollutants, nitrogen oxides (NO) stand out as particularly harmful irritant gases, known to cause airway inflammation at elevated concentrations. Chemiresistive gas sensing (CGS) has revolutionized gas detection with its low power consumption, cost-effectiveness, high sensitivity, fast response, and long-term stability. Traditional materials such as metal oxides, conducting polymers, and carbon-based materials used for NO detection often suffer from poor selectivity and require high operating temperatures, leading to high noise levels.
View Article and Find Full Text PDFACS Sens
August 2025
National Key Laboratory of Advanced Micro and Nano Manufacture Technology, Shanghai Jiao Tong University, Shanghai 200240, China.
The rapid growth of the electric vehicle industry has raised concerns about battery thermal runaway, which poses serious safety risks. Real-time detection of characteristic gases is crucial for early warning, but there is a lack of highly sensitive and selective gas-sensing materials, especially for carbon monoxide (CO) detection at room temperature in oxygen-free environments. Here, a novel one-dimensional (1D) conductive metal-organic framework (MOF) is synthesized as a highly sensitive and selective room-temperature CO gas-sensing material for battery thermal runaway detection.
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