Search Results (313)

Efficient detection of toxic and flammable vapors remains a major technological challenge, especially for environmental and industrial applications. This paper reports on the fabrication technology and gas-sensing properties of nanostructured Ga₂O₃/GaS_0.98Se_0.02. The β-Ga₂O₃ nanowires/nanoribbons with inclusions of Ga₂S₃ and Ga₂Se₃ microcrystallites were obtained by thermal treatment of GaS_0.98Se_0.02 slabs in air enriched with water vapors. The microstructure, crystalline quality, and elemental composition of the obtained samples were investigated using electron microscopy, X-ray diffraction, and Raman spectroscopy. The obtained structures show promising results as active elements in gas sensor applications. Vapors of methanol (CH₃OH), ethanol (C₂H₅OH), and acetone (CH₃-CO-CH₃) were successfully detected using the nanostructured samples. The electrical signal for gas detection was enhanced under UV light irradiation. The saturation time of the sensor depends on the intensity of the UV radiation beam. Full article

Hydrogen (H₂) gas sensors are essential for detecting leaks and ensuring safety, thereby supporting the broader adoption of hydrogen energy. The performance of H₂ sensors has been shown to be improved by the incorporation of TiO₂ nanostructures. The key findings are summarized as follows: (1) Resistive random-access memory (ReRAM) technology was used to fabricate extremely compact H₂ sensors via various forming techniques, and substantial sensor performance enhancement was investigated. (2) A nanocontact composed of titanium oxide (TiO_x)/platinum (Pt) was subjected to various forming operations to establish a Schottky junction with a nanogap structure on a tantalum oxide (Ta₂O₅) layer, and its properties were assessed. (3) When the Pt electrode was on the positive side during the forming operation used for ReRAM technology, a Pt nanopillar structure was produced. By contrast, when the forming operation was conducted with a positive bias on the TiO_x side, a mixed oxide film of Ta and Ti was produced, which indicates local Ta doping into the TiO_x. A sensor response of over 1000 times was achieved at a minimal voltage of 1 mV at room temperature. (4) This sensor fabrication technology based on the forming operation is promising for the development of low-power consumption sensors. Full article

As lithium-ion batteries (LIBs) gain widespread use, detecting electrolyte–vapor emissions during early thermal runaway (TR) remains critical to ensuring battery safety; yet, it remains understudied. Gas sensors integrating oxide nanostructures offer a promising solution as they possess high sensitivity and fast response, enabling rapid detection of various gas-phase indicators of battery failure. Utilizing this approach, 3D ordered tin oxide (SnO₂) nanostructures were synthesized using polystyrene sphere (PS) templates of varied diameters (200–1500 nm) and precursor concentrations (0.2–0.6 mol/L) to detect key electrolyte–vapors, especially ethyl methyl carbonate (EMC), released in the early stages of TR. The 3D ordered SnO₂ nanostructures with ring- and nanonet-like morphologies, formed after PS template removal, were characterized, and the effects of template size and precursor concentration on their structure and sensing performance were investigated. Among various nanostructures of SnO₂, nanonets achieved by a 1000 nm PS template and 0.4 mol/L precursor showed higher mesoporosity (~28 nm) and optimal EMC detection. At 210 °C, it detected 10 ppm EMC with a response of ~7.95 and response/recovery times of 14/17 s, achieving a 500 ppb detection limit alongside excellent reproducibility/stability. This study demonstrates that precise structural control of SnO₂ nanostructures using templates enables sensitive EMC detection, providing an effective sensor-based strategy to enhance LIB safety. Full article

Glancing Angle Deposition (GLAD) has emerged as a versatile and powerful nanofabrication technique for developing next-generation gas sensors by enabling precise control over nanostructure geometry, porosity, and material composition. Through dynamic substrate tilting and rotation, GLAD facilitates the fabrication of highly porous, anisotropic nanostructures, such as aligned, tilted, zigzag, helical, and multilayered nanorods, with tunable surface area and diffusion pathways optimized for gas detection. This review provides a comprehensive synthesis of recent advances in GLAD-based gas sensor design, focusing on how structural engineering and material integration converge to enhance sensor performance. Key materials strategies include the construction of heterojunctions and core–shell architectures, controlled doping, and nanoparticle decoration using noble metals or metal oxides to amplify charge transfer, catalytic activity, and redox responsiveness. GLAD-fabricated nanostructures have been effectively deployed across multiple gas sensing modalities, including resistive, capacitive, piezoelectric, and optical platforms, where their high aspect ratios, tailored porosity, and defect-rich surfaces facilitate enhanced gas adsorption kinetics and efficient signal transduction. These devices exhibit high sensitivity and selectivity toward a range of analytes, including NO₂, CO, H₂S, and volatile organic compounds (VOCs), with detection limits often reaching the parts-per-billion level. Emerging innovations, such as photo-assisted sensing and integration with artificial intelligence for data analysis and pattern recognition, further extend the capabilities of GLAD-based systems for multifunctional, real-time, and adaptive sensing. Finally, current challenges and future research directions are discussed, emphasizing the promise of GLAD as a scalable platform for next-generation gas sensing technologies. Full article

Acetone detection is crucial for non-invasive health monitoring and environmental safety, so there is an urgent demand to develop high-performance gas sensors. Here, platinum (Pt)-functionalized layered flower-like nickel ferrite (NiFe₂O₄) sheets were efficiently fabricated via facile hydrothermal synthesis and wet chemical reduction processes. When the Ni/Fe molar ratio is 1:1, the sensing material forms a Ni/NiO/NiFe₂O₄ composite, with performance further optimized by tuning Pt loading. At 1.5% Pt mass fraction, the sensor shows a high acetone response (R_g/R_a = 58.33 at 100 ppm), a 100 ppb detection limit, fast response/recovery times (7/245 s at 100 ppm), and excellent selectivity. The enhancement in performance originates from the synergistic effect of the structure and Pt loading: the layered flower-like morphology facilitates gas diffusion and charge transport, while Pt nanoparticles serve as active sites to lower the activation energy of acetone redox reactions. This work presents a novel strategy for designing high-performance volatile organic compound (VOC) sensors by combining hierarchical nanostructured transition metal ferrites with noble metal modifications. Full article

Carbon nanotubes (CNTs) have emerged as pivotal nanomaterials in sensing technologies owing to their unique structural, electrical, and mechanical properties. Their high aspect ratio, exceptional surface area, excellent electrical conductivity, and chemical tunability enable superior sensitivity and rapid response in various sensor platforms. This review presents a comprehensive overview of recent advancements in CNT-based sensors, encompassing both single-walled (SWCNTs) and multi-walled carbon nanotubes (MWCNTs). We discuss their functional roles in diverse sensing applications, including gas sensing, chemical detection, biosensing, and pressure/strain monitoring. Particular emphasis is placed on the mechanisms of sensing, such as changes in electrical conductivity, surface adsorption phenomena, molecular recognition, and piezoresistive effects. Furthermore, we explore strategies for enhancing sensitivity and selectivity through surface functionalization, hybrid material integration, and nanostructuring. The manuscript also covers the challenges of reproducibility, selectivity, and scalability that hinder commercial deployment. In addition, emerging directions such as flexible and wearable CNT-based sensors, and their role in real-time environmental, biomedical, and structural health monitoring systems, are critically analyzed. By outlining both current progress and existing limitations, this review underscores the transformative potential of CNTs in the design of next-generation sensing technologies across interdisciplinary domains. Full article

The rise of two-dimensional (2D) materials has transformed gas sensing, with Nb₂CT_x MXene drawing significant interest due to its distinct physicochemical behaviors. As part of the MXene family, Nb₂CT_x MXene demonstrates a remarkable combination of high electrical conductivity, adjustable surface chemistry, and exceptional mechanical flexibility, positioning it as a promising candidate for next-generation gas sensors. This review explores the synthesis techniques for Nb₂CT_x MXene, highlighting etching methods and post-synthesis adjustments to achieve the tailored surface terminations and structural qualities essential for gas detection. A comprehensive examination of the crystal structure, morphology, and electronic characteristics of Nb₂CT_x MXene is presented to clarify its outstanding sensing capabilities. The application of Nb₂CT_x MXene for detecting gases, including NH₃, humidity, NO₂, and volatile organic compounds (VOCs), is assessed, showcasing its sensitivity, selectivity, and low detection limits across various environmental settings. Furthermore, the integration of Nb₂CT_x MXene with other nanostructures in sensor platforms is reviewed. Lastly, challenges related to scalability, stability, and long-term performance are addressed, along with future prospects for Nb₂CT_x MXene-based gas sensors. This review offers significant insights into the potential of Nb₂CT_x MXene as a pioneering material for enhancing gas sensing technologies. Full article

Molybdenum disulfide (MoS₂) has gained attention for its promising gas-sensing capabilities due to its high surface area and tunable electronic properties. In this study, we investigate the time-dependent growth (under constant conditions) of sputtered MoS₂ films on ZnO nanorods and their impact on NO₂ sensing performance. ZnO nanorods, synthesized via a hydrothermal method, provide a high-surface-area template to enhance charge transport and gas adsorption. Gas-sensing experiments revealed a strong correlation between MoS₂ thickness and NO₂ response, with the 25-min-sputtered MoS₂ film exhibiting the highest response of 20.9%. The synergistic interaction between MoS₂ and ZnO nanorods facilitated charge transfer and enhanced adsorption sites for NO₂ molecules. These findings emphasize the critical role of time-dependent growth of MoS₂ film in modulating gas-sensing performance and provide insights into designing high-sensitivity NO₂ sensors at room temperature. This study contributes to the development of hybrid MoS₂/ZnO nanostructures for next-generation environmental monitoring applications. Full article

Gas-sensing technology is crucial for the detection of toxic and harmful gases to ensure environmental safety and human health. Gas sensors convert the changes in the conductivity of the sensing material resulting from the adsorption of gas molecules into measurable electrical signals. Rare earth orthoferrite-based perovskite oxides have emerged as promising candidates for gas-sensing technology owing to their exceptional structural, optical, and electrical properties, which enable the detection of various gases. In this article, we review the latest developments in orthoferrite-based gas sensors in terms of sensitivity, selectivity, stability, operating temperature, and response and recovery times. It begins with a discussion on the gas-sensing mechanism of orthoferrites, followed by a critical emphasis on their nanostructure, doping effects, and the formation of nanocomposites with other sensing materials. Additionally, the role of the tunable bandgap and different porous morphologies with a high surface area of the orthoferrites on their gas-sensing performance were explored. Finally, we identified the current challenges and future perspectives in the gas-sensing field, such as novel doping strategies and the fabrication of miniaturized gas sensors for room-temperature operation. Full article

The challenging problem of chlorine “poisoning” SnO₂ for poorly recoverable detection of dichloromethane has been solved in this work. The materials synthesized by Ni or/and Mo doping SnO₂ were spread onto the micro-hotplates (<1 mm³) to fabricate the MEMS sensors with a low power consumption (<45 mW). The sensor based on Mo·Ni co-doped SnO₂ is evidenced to have the best sensing performance of significant response and recoverability to dichloromethane between 0.07 and 100 ppm at the optimized temperature of 310 °C, in comparison with other sensors in this work and the literature. It can be attributed to a synergetic effect of Mo·Ni co-doping into SnO₂ as being supported by characterization of geometrical and electronic structures. The sensing mechanism of dichloromethane on the material is investigated. In situ infrared spectroscopy (IR) peaks identify that the corresponding adsorbed species are too strong to desorb, although it has demonstrated a good recoverability of the material. A probable reason is the formation rates of the strongly adsorbed species are much slower than those of the weakly adsorbed species, which are difficult to form significant IR peaks but easy to desorb, thus enabling the material to recover. Theoretical analysis suggests that the response process is kinetically determined by molecular transport onto the surface due to the free convection from the concentration gradient during the redox reaction, and the output steady voltage thermodynamically follows the equation only formally identical to the Langmuir–Freundlich equation for physisorption but is newly derived from statistical mechanics. Full article

In this work, room-temperature UV-assisted ozone detection was investigated using ZnO nanoplates synthesized via precipitation, ultrasound-, ultrasonic tip-, and microwave-assisted hydrothermal (MAH) methods. X-ray diffraction confirmed the formation of crystalline phases with an ~3.3 eV band gap, independent of the synthesis used. Raman spectroscopy revealed oxygen-related defects. Plate-like morphologies were observed, with the ultrasonic tip-assisted synthesis yielding ~17 nm-thick plates. Electrical measurements showed 10–170 ppb ozone sensitivity under UV. The sample synthesized via the MAH method (ZM) demonstrated superior conductance, with a baseline resistance of ~1.2% for the ultrasound (ZU) sample and less than 50% for the precipitation (ZA) and ultrasonic tip (ZP) samples. Despite the appreciable response in dark mode, the recovery was slow (>>30 min), except for the UV illumination condition, which reduced the recovery response to ~2 min. With top areas of ~0.0122 µm², ZP and ZU showed high specific surface areas (24.75 and 19.37 m²/g, respectively), in contrast to ZM, which exhibited the lowest value (15.32 m²/g) with a top area of ~0.0332 µm² and a thickness of 26.0 nm. The superior performance of ZM was attributed to the larger nanoplate sizes and the lower baseline resistance. The ultrasound method showed the lowest sensitivity due to the higher resistance and the depletion layer effect. The results indicate that the synthesis methods presented herein for the production of reactive ZnO nanoplates using NaOH as a growth-directing agent are reliable, simple, and cost-effective, in addition to being capable of detecting ozone with high sensitivity and reproducibility at concentrations as low as 10 ppb. Full article

Using the Bridgman technique, GaSe single crystals were obtained which were mechanically split into plane-parallel plates with a wide range of thicknesses. By heat treatment in air at 820 °C and 900 °C, for 30 min and 6 h, micro- and nanocomposite layers of Ga₂Se₃–Ga₂O₃ and β–Ga₂O₃ (native oxide) with surfaces made of nanowires/nanoribbons were obtained. The obtained composite Ga₂Se₃–Ga₂O₃ and nanostructured β–Ga₂O₃ are semiconductor materials with band gaps of 2.21 eV and 4.60 eV (gallium oxide) and photosensitivity bands in the green–red and ultraviolet-C regions that peaked at 590 nm and 262 nm. For an applied voltage of 50 V, the dark current in the photodetector based on the nanostructured β–Ga₂O₃ layer was of 8.0 × 10⁻¹³ A and increased to 9.5 × 10⁻⁸ A upon 200 s excitation with 254 nm-wavelength radiation with a power density of 15 mW/cm². The increase and decrease in the photocurrent are described by an exponential function with time constants of τ_1r = 0.92 s, τ_2r = 14.0 s, τ_1d = 2.18 s, τ_2d = 24 s, τ_1r = 0.88 s, τ_2r = 12.2 s, τ_1d = 1.69 s, and τ_2d = 16.3 s, respectively, for the photodetector based on the Ga₂Se₃–Ga₂S₃–GaSe composite. Photoresistors based on the obtained Ga₂Se₃–Ga₂O₃ composite and nanostructured β–Ga₂O₃ layers show photosensitivity bands in the spectral range of electronic absorption bands of ozone in the same green–red and ultraviolet-C regions, and can serve as ozone sensors (detectors). Full article

The demand for reliable and cost-effective CO₂ gas sensors is escalating due to their extensive applications in various sectors such as food packaging, indoor air quality assessment, and real-time monitoring of anthropogenic CO₂ emissions to mitigate global warming. Nanostructured materials exhibit exceptional properties, including small grain size, controlled morphology, and heterojunction effects, rendering them promising candidates for chemiresistive CO₂ gas sensors. This review article provides an overview of recent advancements in chemiresistive CO₂ gas sensors based on nanostructured semiconducting materials. Specifically, it discusses single oxide structures, metal-decorated oxide nanostructures, and heterostructures, elucidating the correlations between these nanostructures and their CO₂ sensing properties. Additionally, it addresses the challenges and future prospects of chemiresistive CO₂ gas sensors, aiming to provide insights into the ongoing developments in this field. Full article

Resistive gas sensors are among the most widely used sensors for the detection of various gases. In this type of gas sensor, the gas sensing capability is linked to the surface properties of the sensing layer, and accordingly, modification of the sensing surface is of importance to improve the sensing output. Plasma treatment is a promising way to modify the surface properties of gas sensors, mainly by changing the amounts of oxygen ions, which have a central role in gas sensing reactions. In this review paper, we focus on the role of plasma treatment in the gas sensing features of resistive gas sensors. After an introduction to air pollution, toxic gases, and resistive gas sensors, the main concepts regarding plasma are presented. Then, the impact of plasma treatment on the sensing characteristics of various sensing materials is discussed. As the gas sensing field is an interdisciplinary field, we believe that the present review paper will be of significant interest to researchers with various backgrounds who are working on gas sensors. Full article

This paper presents a novel approach for fabricating porous NiO films decorated with nanowires, achieved through sputtering followed by thermal oxidation of a metallic layer. Notably, we successfully fabricate NiO nanowires using this simple and cost-effective method, demonstrating its potential applicability in the gas-sensing field. Furthermore, by using the film of our nanowires, we are able to easily prepare NiO sensors and deposit the required Pt electrodes directly on the film. This is a key advantage, as it simplifies the fabrication process and makes it easier to integrate the sensors into practical gas-sensing devices without the need for nanostructure transfer or intricate setups. Scanning electron microscopy (SEM) reveals the porous structure and nanowire formation, while X-ray diffraction (XRD) confirms the presence of the NiO phase. As a preliminary investigation, the gas-sensing properties of NiO films with varying thicknesses were evaluated at different operating temperatures. The results indicate that thinner layers exhibit superior performances. Gas measurements confirm the p-type nature of the NiO samples, with sensors showing high responsiveness and selectivity toward NO₂ at an optimal temperature of 200 °C. However, incomplete recovery is observed due to the high binding energy of NO₂ molecules. At higher temperatures, sufficient activation energy enables a full sensor recovery but with reduced response. The paper discusses the adsorption–desorption reaction mechanisms on the NiO surface, examines how moisture impacts the enhanced responsiveness of Pt-NiO (2700%) and Au-NiO (400%) sensors, and highlights the successful fabrication of NiO nanowires through a simple and cost-effective method, presenting a promising alternative to more complex approaches. Full article