In this work, WO₃/TiO₂ core–shell (C-S) nanowires (NWs) were successfully synthesized by the coaxial electrospinning method and subsequent high-temperature calcination treatment. After some microscopic structural characterizations, although the prepared WO₃–TiO₂ and TiO₂–WO₃ C-S NWs displayed quite different surface morphologies, both of the shell coatings were uniform and their typical shell thicknesses were extremely close, with mean values of 22 and 20 nm, respectively. In gas sensing tests, WO₃/TiO₂ C-S NWs exhibited good selectivity towards triethylamine (TEA) without significant interfering gases. Compared with bare WO₃ and TiO₂ NWs, WO₃/TiO₂ C-S NWs showed better gas sensing performance. Specifically, the optimal operating temperature and response of TiO₂–WO₃ C-S NWs to 100 ppm TEA were 130 °C and 106, which were reduced by 70 °C and increased by 5.73 times compared to bare WO₃, respectively. Obviously, the C-S nanostructures contributed to improving the gas sensing performance of materials towards TEA. Finally, some hypothetical sensing mechanisms were proposed, which were expected to have important reference significance for the design of target products applied to TEA sensing.

In this study, a terahertz microfluidic multi-band sensor was designed. Unlike previous microfluidic absorption sensors that rely on dipole resonance, the proposed sensor uses a physical mechanism for absorption by exciting higher-order lattice resonances in microfluidic structures. With a Fabry–Perot cavity, the sensor can form an absorption peak with a high quality factor (Q) and narrow full width at half maximum (FWHM). A high Q value and a narrow FWHM are valuable in the field of sensing and provide strong support for high-precision sensing. On this basis, the sensing performance of the device was investigated. The simulation results clearly show that the absorption sensor has ultra-high sensitivity, which reaches 400 GHz/Refractive Index Unit (RIU). In addition, the sensor generates three absorption peaks, overcoming the limitations of a single frequency band in a composite resonance mode and multidimensional frequency response, which has potential application value in the field of volatile organic compound (VOC) sensing.

Seafood, especially marine fish, is highly prone to spoilage during processing, transportation, and storage. It releases pungent trimethylamine (TMA) gas, which severely affects food quality and safety. Metal–oxide–semiconductor (MOS) gas sensors for TMA detection offer a rapid, convenient, and accurate method for assessing fish freshness. Indium oxide (In₂O₃) has shown potential as an effective sensing material for the detection of TMA. In this work, one-dimensional In₂O₃ nanowires with different grain sizes and levels of crystallinity were synthetized using the electrospinning technique and underwent different thermal calcination processes. Gas-sensing tests showed that the In₂O₃–3 °C/min–500 °C gas sensor exhibited an outstanding performance, including a high response (R_a/R_g = 47.0) to 100 ppm TMA, a short response time (6 s), a low limit of detection (LOD, 0.0392 ppm), and an excellent long-term stability. Furthermore, the sensor showed promising experimental results in monitoring the freshness of Larimichthys crocea (L. crocea). By analyzing the relationship between the grain size and crystallinity of the In₂O₃ samples, a mechanism for the enhanced gas-sensing performance was proposed. This work provides a novel strategy for designing and fabricating gas sensors for TMA detection and highlights their potential for broad applications in real-time fish freshness monitoring.

In recent years, paper-based humidity sensors have emerged as a highly promising technology for humidity detection. In this work, a polymerizable deep eutectic solvent (PDES) was prepared via a one-step blending method, which was applied to modify filter paper. The modification process did not alter the overall structure of the paper cellulose but rather targeted only its internal cellulose channels, thereby minimizing any impact on the paper’s original moisture-independent properties. The filter paper functioned both as the substrate and the humidity-sensing material in the fabricated sensor. The finger-like electrodes were designed using AutoCAD 2018 software and then printed onto the modified paper using screen-printing technology to fabricate the humidity sensor. Different saturated salt solutions were used to simulate corresponding humidity environments and evaluate the humidity performance of sensors. Compared with that of the blank paper-based humidity sensor, the sensitivity of the sensor modified by the PDES was significantly greater, and the recovery time was greatly shorter. Specifically, the sensitivity increased from 1.34 to 10.36 at 54% RH and from 166.24 to 519.2 at 98% RH. Additionally, the sensor response time was reduced from 728 s to 137 s. PDES modification significantly improved the moisture-sensitive characteristics and detection performance of the sensor.