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This study presents the design and development of an innovative optical dual gas sensor tailored for biomedical applications, enabling the simultaneous detection of nitric oxide (NO) and oxygen (O2), critical biomarkers in physiological monitoring. The sensor leverages electrospun fibers embedded with CsPbBr3 quantum dots (QDs) and platinum(II) meso-tetrakis(pentafluorophenyl) porphyrin (PtTFPP), offering a novel approach to enhancing gas-sensing capabilities. Electrospinning produces highly porous, uniform cellulose acetate fibers under optimized conditions (5 mL/hour flow rate, 17 kV supply voltage, 15 cm working distance), creating a biocompatible matrix that enhances sensor stability and responsiveness. The sensor is excited by a UV LED light source at 380 nm, with fluorescence intensities measured via spectrometry. It demonstrates excellent sensitivity, with maximum sensitivities of 4.2 for nitric oxide and 7.6 for oxygen, and rapid response/recovery times of 90 s/119 s for nitric oxide and 61 s/66 s for oxygen, respectively. These findings highlight the sensor’s potential for high-sensitivity, selective, and fast-response gas detection, making it a promising tool for real-time monitoring of respiratory gases and other biomedical applications.

The coaxial electrospinning method is widely used in a wide range of applications, including medical devices and sensing technology. This study proposes a novel optical dual sensor for simultaneous detection of oxygen (O2) and ammonia (NH3) based on coaxial electrospinning method to produce core-shell fiber membrane doped fluorescent dyes. The O2 (core) and NH3 (shell) sensitive dye membranes were successfully fabricated using coaxial electrospinning method by dissolving a polymer matrix, cellulose acetate (CA), with platinum (II) meso-tetrakis (pentafluorophenyl) porphyrin (PtTFPP) and Eosin-Y, respectively. The optical dual sensor was illuminated by an UV LED to monitor the intensity change and wavelength shift in the presence of selected analyte gases. The experimental data show that the sensitivities of optical dual sensor were found to be 6.4 and 3.2 for O2 and NH3, respectively. The response and recovery times of O2 and NH3 sensing probes were measured to be 12 s/29 s and 65 s/66 s, respectively. Also, when exposed to NH3 gas gradually from 0 to 500 ppm, the wavelength shift data of Eosin-Y was started at 569.5 nm, 573.9 nm, 578.4 nm, 579.4 nm, 580.8 nm, and 582.2 nm, respectively. In applications, the proposed optical dual sensor based on coaxial electrospinning method can detect O2 and NH3 gases simultaneously.

This work presents a new optical dual sensor based on PtTFPP-containing electrospun fibers and CsPbBr3 perovskite quantum dots (PQDs) for simultaneous detection of oxygen (O2) and nitric oxide (NO) gases, wherein PtTFPP-containing electrospun fibers for O2 sensing was based on electrospinning process fabricated by platinum(II) meso-tetrakis (pentafluorophenyl) porphyrin (PtTFPP) complex immobilized in cellulose acetate (CA) matrix. CsPbBr3 PQDs were used as NO-sensitive material and coated on the surface of PtTFPP-containing electrospun fibers. Both materials were excited by a UV LED with a central wavelength of 380 nm, and the fluorescence intensities of sensing materials were recorded and analyzed with a spectrometer. The experiment results show that the optical NO and O2 sensors have linear Stern–Volmer plots, and the sensitivities are around 2.7 and 10.7, respectively. The response and recovery times of the optical NO sensor are 71 and 109 s, respectively. For optical O2, response and recovery times are 60 and 65 s, respectively. The optical dual sensor with a new method based on fluorescent dye containing electrospun fibers and coated with CsPbBr3 PQDs has been successfully developed to detect NO and O2 gases simultaneously. The optical dual gas sensor provides great potential for practical applications with low cost and ease of fabrication.

Sensitivity is one of the crucial factors in determining the quality of a fluorescence/phosphorescence-based gas sensor, and is estimated from the measurement of responses (I0/I, where I0 and I refer to the measured optical intensity of a sensor in absence and presence of analyte molecules) at various concentrations of analytes. In this work, we demonstrate phosphorescence-based optical oxygen sensors fabricated on highly porous anodic aluminum oxide (AAO) membranes showing dramatically high response. These sensors exploit the enormous surface area of the AAO to facilitate the effective interaction between the sensing molecules and the analytes. We spin-coat an AAO membrane (200 nm pore diameter) with a platinum-based oxygen sensing porphyrin dye, platinum(II) meso-tetrakis (pentafluorophenyl) porphyrin (PtTFPP), to fabricate a sensor exhibiting I0/I ~400 at 100% oxygen atmosphere. To address the generality of the AAO membrane, we fabricate a separate sensor with another porphyrin dye, platinum octaethylporphyrin (PtOEP), which exhibits an even higher I0/I of ~500. Both of these sensors offer the highest responses as an optical oxygen sensor hitherto reported. SEM and EDS analysis are performed to realize the effect of the increased surface area of the AAO membrane on the enhanced sensitivity.

Surface-enhanced Raman scattering (SERS) has been widely used to effectively detect various biological and organic molecules. This detection method needs analytes adsorbed onto a specific metal nanostructure, e.g., Ag-nanoparticles. A substrate containing such a structure (called SERS substrate) is user-friendly for people implementing the adsorption and subsequent SERS detection. Here, we report on powerful SERS substrates based on efficient fabrication of Ag-filled anodic aluminum oxide (AAO) films. The films contain many nanopores with small as-grown inter-pore gap of 15 nm. The substrates are created by electrochemically depositing silver into nanopores without an additional pore widening process, which is usually needed for conventional two-step AAO fabrication. The created substrates contain well-separated Ag-nanoparticles with quite a small inter-particle gap and a high number density (2.5 × 1010 cm−2). We use one-step anodization together with omitting additional pore widening to improve the throughput of substrate fabrication. Such substrates provide a low concentration detection limit of 10−11 M and high SERS enhancement factor of 1 × 106 for rhodamine 6G (R6G). The effective detection of biological and organic molecules by the substrate is demonstrated with analytes of adenine, glucose, R6G, eosin Y, and methylene blue. These results allow us to take one step further toward the successful commercialization of AAO-based SERS substrates.