A novel optical fiber array-type of sensing instrument with temperature compensation for real-time detection was developed to measure oxygen, carbon dioxide, and ammonia simultaneously. The proposed instrument is multi-sensing array integrated with real-time measurement module for portable applications. The sensing optical fibers were etched and polished before coating to increase sensitivities. The ammonia and temperature sensors were each composed of a dye-coated single-mode fiber with constructing a fiber Bragg grating and a long-period filter grating for detecting light intensity. Both carbon dioxide and oxygen sensing structures use multimode fibers where 1-hydroxy-3,6,8-pyrene trisulfonic acid trisodium salt is coated for carbon dioxide sensing and Tris(2,2′-bipyridyl) dichlororuthenium(II) hexahydrate and Tris(bipyridine)ruthenium(II) chloride are coated for oxygen sensing. Gas-induced fluorescent light intensity variation was applied to detect gas concentration. The portable gas sensing array was set up by integrating with photo-electronic measurement modules and a human-machine interface to detect gases in real time. The measured data have been processed using piecewise-linear method. The sensitivity of the oxygen sensor were 1.54%/V and 9.62%/V for concentrations less than 1.5% and for concentrations between 1.5% and 6%, respectively. The sensitivity of the carbon dioxide sensor were 8.33%/V and 9.62%/V for concentrations less than 2% and for concentrations between 2% and 5%, respectively. For the ammonia sensor, the sensitivity was 27.78%/V, while ammonia concentration was less than 2%.
Field-effect transistor (FET)-based biosensors are powerful analytical tools for detecting trace-specific biomolecules in diverse sample matrices, especially in the realms of pandemics and infectious diseases. The primary concern in applying these biosensors is their stability, a factor directly impacting the accuracy and reliability of sensing over extended durations. The risk of biosensor degradation is substantial, potentially jeopardizing the sensitivity and selectivity and leading to inaccurate readings, including the possibility of false positives or negatives. This paper delves into the documented degradation of silicon nanobelt FET (NBFET) biosensors induced by buffer solutions. The results highlight a positive correlation between immersion time and the threshold voltage of NBFET devices. Secondary ion mass spectrometry analysis demonstrates a gradual increase in sodium and potassium ion concentrations within the silicon as immersion days progress. This outcome is ascribed to the nanobelt’s exposure to the buffer solution during the biosensing period, enabling ion penetration from the buffer into the silicon. This study emphasizes the critical need to address buffer-solution-induced degradation to ensure the long-term stability and performance of FET-based biosensors in practical applications.
A new-type vibration sensor based on a fiber Bragg grating combined with a special structure-packaged design is proposed for monitoring the mechanical vibration signals. Three different sensing structures, including the film squeeze type, new film squeeze type, and elastic tape squeeze type are proposed for measuring the vibration signals with the frequency range from tens to thousands of Hz. In the comparison to experimental results, the new film squeeze structure has a nice sensing performance in the range from 100 to 1000 Hz with a sensitivity of 0.302 mV/g. For the elastic tape squeeze structure, the elastic tape is designed to encapsulate the optical fiber with a good frequency response from 1100 to 3100 Hz. In addition, by using the new film squeeze structure to measure the steady-state and non-steady-state vibration signals, the spectral components of sensing signals are analyzed by using the wavelet transformation for confirming the testing signals. These vibration fiber sensors can be applied in the measurement of high-end manufacture-facility vibration or earthquake vibrations etc.
This paper presents a high-sensitivity two-dimensional fiber-optic hydrophone designed for the detection and localization of underwater acoustic sources. The device comprises two sensing heads, each incorporating a fiber Bragg grating (FBG) embedded within a customized 3D-printed encapsulation. To enhance acoustic sensitivity, the design utilizes a silicone thin-film coupled with a pyramidal channel that spatially concentrates acoustic energy from the base to the apex, where the FBG is positioned. Incident acoustic pressure induces vibrations in the film, which are amplified by the channel structure, imparting strain on the FBG and resulting in a shift in the Bragg wavelength. The acoustic frequency response is demodulated by converting the overlapping optical power between the sensing and reference gratings into an electrical signal via a photodetector. By arranging the two sensing heads orthogonally, the system effectively determines the direction and angle of the acoustic source. Experimental results show a peak sensitivity of −210.59 dB re 1 V/μPa, with a FWHM of 57.92–66.27 Hz and a figure of merit (FOM) up to 3.64 dB/Hz. In addition, the acoustic-field SNR is approximately 26 dB in the dominant band, and the LOD is 64.19 dB re 1 μPa (10–400 Hz). Experimental validation confirms the hydrophone’s high sensitivity and localization accuracy, demonstrating its significant potential for underwater acoustic sensing applications.
Field-effect transistor (FET)-based biosensors stand as powerful analytical tools for detecting trace-specific biomolecules in diverse sample matrices, especially in the realms of pandemics and infectious diseases. The primary concern in applying these biosensors is their stability, a factor directly impacting the accuracy and reliability of sensing over extended durations. The risk of biosensor degradation is substantial, potentially jeopardizing sensitivity and selectivity and leading to inaccurate readings, including the possibility of false positives or negatives. This paper delves into the documented degradation of silicon nanobelt FET (NBFET) biosensors induced by buffer solutions. The results highlight a positive correlation between immersion time and the threshold voltage of NBFET devices. Secondary ion mass spectrometry analysis demonstrates a gradual increase in sodium and potassium ion concentrations within the silicon as immersion days progress. This outcome is ascribed to the nanobelt's exposure to the buffer solution during the biosensing period, enabling ion penetration from the buffer into the silicon. The study emphasizes the critical need to address buffer solution-induced degradation to ensure the long-term stability and performance of FET-based biosensors in practical applications.
Optically controlled non-volatile memory devices represent a promising paradigm for next-generation data storage, offering advantages such as high-speed, non-contact operation, and robust immunity to electromagnetic interference. In this study, an organic photomemory device with excellent photo-switching capabilities was fabricated using polyimide thin films. The resistive switching mechanism is attributed to a reversible molecular transformation between insulating aromatic and conductive quinoid moieties. Under UVA irradiation, the device transitions from a high resistance state (HRS) to a low resistance state in an ultrafast “Write” operation, inducing a current increase of over eight orders of magnitude (from ∼10−12 to ∼10−3 A). Conversely, a targeted UVC irradiation for ∼25 s executes the “Erase” operation, restoring the HRS. To address the inherent temporal asymmetry between these processes, an optimized wavelength-selective strategy is proposed, utilizing the UVA band for programming and the UVC band for erasing. This dual-band approach effectively mitigates spectral crosstalk, significantly enhancing the device’s operational efficiency, contrast, and cyclic stability, while maintaining a robust data retention of ∼14 000 s.