Polycyclic aromatic hydrocarbons (PAHs) are increasingly recognized as a major contributor to the occupational cancer risk among firefighters. In response, the National Fire Protection Association (NFPA) and other regulatory bodies have recommended rigorous decontamination protocols to minimize PAH exposure. Despite these efforts, a critical gap persists: the absence of real-time, field-deployable devices capable of detecting these invisible and toxic compounds during firefighting operations or within fire stations. Additionally, the lack of effective and optimized methods for the removal of these hazardous substances from the immediate environments of firefighters continues to pose a serious occupational health challenge. Although numerous studies have investigated PAH detection in environmental contexts, current technologies are still largely confined to laboratory settings and are unsuitable for field use. This review critically examines recent advances in PAH decontamination strategies for firefighting and explores alternative sensing solutions. We evaluate both conventional analytical methods, such as gas chromatography, high-performance liquid chromatography, and mass spectrometry, and emerging portable PAH detection technologies. By highlighting the limitations of existing systems and presenting novel sensing approaches, this paper aims to catalyze innovation in sensor development. Our ultimate goal is to inspire the creation of robust, field-deployable tools that enhance decontamination practices and significantly improve the health and safety of firefighters by reducing their long-term risks of cancer.

The exploration of the chiral configurations of enantiomers represents a highly intriguing realm of scientific inquiry due to the distinct roles played by each enantiomer (D and L) in chemical reactions and their practical utilities. This study introduces a pioneering analytical methodology, termed fast Fourier transform capacitance voltammetry (FFT-CPV), in conjunction with principal component analysis (PCA), for the identification and quantification of the chiral forms of tartaric acid (TA), serving as a representative model system for materials exhibiting pronounced chiral characteristics. The proposed methodology relies on the principle of chirality, wherein the capacitance signal generated by the adsorption of D-TA and L-TA onto the surface of a platinum electrode (Pt-electrode) in an acidic solution is harnessed. The capacitance voltammograms were meticulously recorded under optimized experimental conditions. To compile the final dataset for the analyte, the average of the FFT capacitance voltammograms of the acidic solution (without the presence of the analyte) was subtracted from those containing the analyte. A distinct arrangement was obtained by employing PCA as a linear data transformation method, representing D-TA and L-TA in a two/three-dimensional space. The outcomes of the study reveal the successful detection of the two chiral forms of TA with a considerable degree of precision and reproducibility. Moreover, the proposed method facilitated the establishment of two linear response ranges for the concentration values of each enantiomer, spanning from 1 to 20 µM, and 50 to 500 µM. The respective detection limits were also determined to be 0.4 µM for L-TA and 1.3 µM for D-TA. These findings underscore the satisfactory sensitivity and efficiency of the proposed method in both qualitative and quantitative assessments of the chiral forms of TA.

This work provides the first demonstration of FFTCCV as a dual-purpose method, serving both as a real-time diagnostic tool and as a phase- and morphology-engineering strategy. By adjusting the scan rate, FFTCCV directs the crystallographic evolution of Ni (OH)₂ on Ni foam—stabilizing α-nanoflakes at 0.7 V·s⁻¹ and β-platelets at 0.007 V·s⁻¹—while simultaneously enabling electrode-resolved ΔQ tracking and predictive state-of-health (SoH) monitoring. This approach enabled the precise regulation of electrode morphology and phase composition, yielding high areal capacitance (546.5 mF·cm⁻² at 5 mA·cm⁻²) with ~75% retention after 3000 cycles. These improvements advance the development of high-performance micro-supercapacitors, facilitating their integration into wearable and miniaturized devices where compact and durable energy storage is required. Beyond performance enhancement, FFTCCV also enabled continuous monitoring of capacitance during extended operation (up to 40,000 s). By recording both anodic and cathodic responses, the method provided time-resolved insights into device stability and revealed characteristic signatures of electrode degradation, phase transitions, and morphological changes. Such detection allows recognition of early failure pathways that are not accessible through conventional testing. This monitoring capability functions as an embedded health sensor, offering a pathway for predictive diagnosis of supercapacitor failure. Such functionality is particularly important for energy-driven actuators and smart materials, where uninterrupted operation and preventive maintenance are critical. FFTCCV therefore provides a scalable strategy for developing energy-autonomous microsystems with improved performance and real-time state-of-health monitoring.

Firefighters are exposed to complex smoke containing volatile, semivolatile, aromatic, and particulate-associated organic contaminants that accumulate on skin, clothing, and protective equipment. Conventional gas sensors monitor only selected airborne species, while passive samplers require laboratory analysis and cannot provide continuous exposure assessment. To address this limitation, we developed a proof-of-concept mass-capacitor that integrates contaminant absorption and electrical sensing within a single polydimethylsiloxane/functionalized carbon nanotube (PDMS/f-CNT) composite coated on interdigitated electrodes (IDEs). Unlike conventional sensors that report the instantaneous concentration of selected compounds, the proposed platform functions as both a sorptive collector and an electrical transducer. It continuously converts contaminant uptake, retention, and release into a time-resolved electrical response. For firefighter applications, this mass-capacitor bridges the gap between passive sorptive samplers and conventional real-time gas sensors. It enables continuous tracking of the cumulative sorbed contamination burden without requiring offline laboratory analysis or restricting the measurement to selected airborne species. A custom potentiostat applied staircase cyclic excitation, while Fast Fourier Transform (FFT)-assisted processing enabled extraction of the differential charge, $\mathsf{\Delta }Q$ as an indicator of contaminant loading. The sensor was evaluated using smoke generated from cotton, paper, wood, and synthetic fibers. Compared with PDMS alone, the PDMS/f-CNT composite produced an approximately 24-fold higher response with minimal humidity interference (≈80% RH). Limits of detection ranged from 0.08 to 0.26 ppm, while repeated smoke exposures produced stepwise increases in ΔQ, demonstrating continuous tracking of cumulative contaminant loading. These results establish the feasibility of the mass-capacitor concept and introduce a new approach for real-time monitoring of the accumulated organic contamination burden rather than the instantaneous concentration of individual airborne compounds.