Picric acid (PA) is an organic substance widely used in industry and military, which poses a great threat to the environment and security due to its unstable, toxic, and explosive properties. Trace detection of PA is also a challenging task because of its highly acidic and anionic character. In this work, silver nanoparticles (AgNPs)-decorated porous silicon photonic crystals (PS PCs) were controllably prepared as surface-enhanced Raman scattering (SERS) substrates using the immersion plating solution. PA and Rhodamine 6G dye (R6G) were used as the analyte to explore the detection performance. As compared with single layer porous silicon, the enhancement factor of PS PCs substrates is increased to 3.58 times at the concentration of 10⁻⁶ mol/L (R6G). This additional enhancement was greatly beneficial to the trace-amount-detection of target molecules. Under the optimized assay condition, the platform shows a distinguished sensitivity with the limit of detection of PA as low as 10⁻⁸ mol/L, the linear range from 10⁻⁴ to 10⁻⁷ mol/L, and a decent reproducibility with a relative standard deviation (RSD) of ca. 8%. These results show that the AgNPs-modified PS PCs substrates could also find further applications in biomedical and environmental sensing.

Inspired by the enhanced gas-sensing performance by the one-dimensional hierarchical structure, one-dimensional hierarchical polyaniline/multi-walled carbon nanotubes (PANI/CNT) fibers were prepared. Interestingly, the simple heating changed the sensing characteristics of PANI from p-type to n-type and n-type PANI and p-type CNTs form p–n hetero junctions at the core–shell interface of hierarchical PANI/CNT composites. The p-type PANI/CNT (p-PANI/CNT) and n-type PANI/CNT (n-PANI/CNT) performed the higher sensitivity to NO₂ and NH₃, respectively. The response times of p-PANI/CNT and n-PANI/CNT to 50 ppm of NO₂ and NH₃ are only 5.2 and 1.8 s, respectively, showing the real-time response. The estimated limit of detection for NO₂ and NH₃ is as low as to 16.7 and 6.4 ppb, respectively. After three months, the responses of p-PANI/CNT and n-PANI/CNT decreased by 19.1% and 11.3%, respectively. It was found that one-dimensional hierarchical structures and the deeper charge depletion layer enhanced by structural changes of PANI contributed to the sensitive and fast responses to NH₃ and NO₂. The formation process of the hierarchical PANI/CNT fibers, p–n transition, and the enhanced gas-sensing performance were systematically analyzed. This work also predicts the development prospects of cost-effective, high-performance PANI/CNT-based sensors.

Novel Ni-doped wurtzite ZnS nanospheres decorated with Au nanoparticles (Au NPs–ZnS NSs) have been successfully fabricated using a simple method involving vacuum evaporation followed by an annealing process. This transition metal-doped gas sensor had high responsivity, extremely fast response and recovery time, and excellent selectivity to formaldehyde at room temperature. The response and recovery time are only 29 s and 2 s, respectively. Since ZnS is transformed into ZnO at a high temperature, superior room temperature-sensing performance can improve the stability and service life of the sensor. The improvement in sensing performance could be attributed to the reduced charge-transfer distance resulting from the creation of a local charge reservoir layer, and the catalytic and spillover effect of Au nanoparticles. The rough and porous spherical structure can also facilitate the detection and diffusion of gases. The as-prepared Au NPs–ZnS NSs are considered to be an extremely promising candidate material for gas sensors, and are expected to have other potential applications in the future.

The multichannel fluorescent sensor array based on nanofibrous membranes loaded with ZnS quantum dots (QDs) was created and demonstrated for the discriminative detection of explosives. The synergistic effect of the high surface-to-volume ratio of QDs, the good permeability of nanofibrous membranes and the differential response introduced by surface ligands was played by constructing the sensing array using nanofibrous membranes loaded with ZnS QDs featuring several surface ligands. Interestingly, although the fluorescence quenching of the nanofibrous membranes is not linearly related to the exposure time, the fingerprint of each explosive at different times is very similar in shape, and the fingerprints of the three explosives show different shapes. Three saturated vapors of nitroaromatic explosives could be reliably detected and discriminated by the array at room temperature. This work is the first step toward devising a monitoring system for explosives in the field of public security and defense. It could, for example, be coupled with the technology of image recognition and large data analysis for a rapid diagnostic test of explosives. This work further highlights the power of differential, multichannel arrays for the rapid and discriminative detection of a wide range of chemicals.