Catalytic Sensor Research Articles

Experimental study on dynamic response performance of hydrogen sensor in confined space under ceiling

With the advancement of Fuel Cell Vehicles (FCVs), detecting hydrogen leaks is critically important in facilities such as hydrogen refilling stations. Despite its significance, the dynamic response performance of hydrogen sensors in confined spaces, particularly under ceilings, has not been comprehensively assessed. This study utilizes a catalytic combustion hydrogen sensor to monitor hydrogen leaks in a confined area. It examines the effects of leak size and placement height on the distribution of hydrogen concentrations beneath the ceiling. Results indicate that hydrogen concentration rapidly decreases within a 0.5–1.0 m range below the ceiling and declines more gradually from 1.0 to 2.0 m. The study further explores the attenuation pattern of hydrogen concentration radially from the hydrogen jet under the ceiling. By normalizing the radius and concentration, it was determined that the distribution conforms to a Gaussian model, akin to that observed in open space jet flows. Utilizing this Gaussian assumption, the model is refined by incorporating an impact reflux term, thereby enhancing the accuracy of the predictive formula.

Laccase mimetics as sensing elements for amperometric assay of 5-hydroxyindoleacetic acid in urine

Monitoring of the levels of 5-hydroxyindole-3-acetic acid (5-HIAA) is of significant importance for diagnostics of carcinoid tumors. We propose simple catalytic electrochemical sensors for the determination of 5-HIAA in urine using laccase and its mimetics. Laccase-like nanozymes (LacNZs) were synthesized via a chemical reduction, and resulting PtMn and MnO2 nanoflowers (NFs) demonstrated laccase-like activity similar to the laccase from the Trametes zonata. In addition, these LacNZs showed enhanced stability under a wide range of pH (3.0–7.5), temperatures (4–70 °C), and ionic strengths (up to 500 mM NaCl). The developed PtMn NF/graphite electrode, similar to a laccase/graphite electrode, can detect 5-HIAA with a high sensitivity (25 000 ± 12 A·M−1·m−2 and 1900 ± 9 A·M−1·m−2, respectively) and have linear ranges of 0.3 – 15 μM and 2 – 50 μM. The sensors work at low working potentials with a detection limit of 0.16 and 1.4 μM, covering the normal and pathologic ranges of 5-HIAA (1–50 μM) content in urine. They have been successfully applied to 5-HIAA assay in urine samples of people with various diseases and revealed good recovery values and reproducibility. Additionally, the LacNZ-sensor has the best stability and can be used up to 20 days.

Molecular nano-I-beam class of materials: options based on configuration, first principles-based optimization and properties

Nanotubes showed merits including high structural strength-to-weight ratio. However, tubes are less favored regarding stiffness and strength. Nano-I-beams are proposed for improved nano-mechanics. Computationally, the study proposes novel molecular designs of I-beam-like shaped structures. A conformation analysis, molecular dynamics and first principles-based optimization are presented. The study proposes options based on the configuration of the molecular nano-I-beam structure providing less number of planes of symmetry and hence more stability than nanotube-like structures. These designs feature a unique geometrical differentiator of having the walls of the out-of-plane hexagonal motif-based molecular nano-I-beam (C60H46) inclined with different inclination angles enabling promising properties. The stability of the proposed nano-I-beam is proved on par with the corresponding nanotube-like structure. First principles-based evidence is provided on the comparable polarizability and the comparable ability to store energy of the supercell of the crystalline slab nano-I-beam in comparison with the corresponding nanotube. A proposed hybrid octa-hexagonal-cubic molecular nano-I-beam (C24H12) remedies the nano-buckling observed in the alike square-octagonal nanostructure. The molecular nano-I-beam exhibits intrinsic switchability that enables the nano-I-beam to be a topological semiconductor/insulator. The results show promising electronic and elastic properties of the proposed nano-I-beams that suit several applications such as their use in capacitors, transistors, insulators, batteries, quantization-based nano-devices, solid lubricant additive to grease, toughening fibers of nanocomposites, hydrophobic films, emissions adsorbents, catalytic sensors, PAH materials for space, and sustainable energy. The molecular nano-I-beam provides the base of the corresponding 2-D crystalline slab nano-I-beams.

Sustainable valorization of waste plastic into nanostructured materials for environmental, energy, catalytic and biomedical applications: A review

The extensive production and utilization of plastic products are inevitable in the current scenario. However, the non-degradable nature of waste plastic generated after use poses a grave concern. Comprehensive efforts are being made to find viable technological solutions to manage the escalating challenge of waste plastic. This review focuses on the progress made in transformation of waste plastic into value-added nanomaterials. An overview is provided of the waste plastic issue on a global level and its ecological impacts. Currently established methodologies for waste plastic management are examined, along with their limitations. Subsequently, state-of-the-art techniques for converting waste plastic into nanostructured materials are presented, with a critical evaluation of their distinct merits and demerits. Several demonstrated technologies and case studies are discussed regarding the utilization of these nanomaterials in diverse applications, including environmental remediation, energy production and storage, catalytic processes, sensors, drug delivery, bioimaging, regenerative medicine and advanced packaging materials. Moreover, challenges and prospects in the commercial level production of waste plastic-derived nanomaterials and their adoption for industrial and practical usage are highlighted. Overall, this work underscores the potential of transforming waste plastic into nanostructured materials for multifaceted applications. The valorization approach presented here offers an integration of waste plastic management and sustainable nanotechnology. The development of such technologies should pave the way toward a circular economy and the attainment of sustainable development goals.

Rational design of stable Cu and AuCu nanoparticles for investigations of size-enhanced SERS applications

BackgroundWhile significant progress has been made to clarify the effects of Au and Ag nanoparticle size on SERS enhancement, research on the size effects of copper nanoparticles and copper-related nanoalloys on SERS enhancement remain scarce. Nanoscale copper (Cu) is important because of its unique sensing and catalytic properties; however, research on its size and compositional effects remains a significant challenge because of the intricate fabrication process and difficulty in preventing oxidation. ResultsOur study elucidated the size-dependent, surface-enhanced Raman scattering (SERS) of Cu NPs, particularly the sensing capabilities of both electromagnetic (EM) SERS at 1.5 × 103 and chemical enhancement (CE) SERS at 3.6 × 104 of approximately 58 nm Cu NPs. Additionally, a solution aging examination revealed preservation of the metal-related core structure, surface plasmon resonance, and SERS features of the PSMA/ONPG-coated Cu NPs for up to 7 days. With the introduction of galvanic replacement reactions and laser ablation syntheses, the incorporation of Au atoms enabled the fabrication of 7–75 nm AuxCuy nanoparticles by using the remaining Cu core after aging in water, which offered precise control over the Cu/Au ratio from 5/95 to 29/71. SERS measurements of the large AuxCuy nanoparticles amplified up to 1.4 × 104 of the EM-mediated vibrational signals from the adsorbed molecules. The strong Au–S chemical bonds of the Au-rich AuxCuy nanocrystals increased the CE SERS to 5.5 × 104, whereas the Au3Cu1 crystals at the AuxCuy interface decreased the CE SERS but improved the electron transfer for catalysis via SERS detection. SignificanceOur research provides further insight into the structural and size effects of Cu and AuCu alloys used as SERS enhancers and offers avenues for designing cutting-edge SERS catalytic sensors tailored to Cu-related catalytic reactive structures.For the first time, we also manipulated the Cu atomic structure and surface composition to understand the significance of surface effects on SERS substrates of the Cu series from a nanoscale analytical perspective.

Measurements of atomic hydrogen recombination coefficients and the reduction of Al2O3 using a heat flux sensor

The knowledge of atomic hydrogen recombination coefficient (γ) is essential for plasma simulations to calculate accurate atomic hydrogen fluxes. However, γ is a complex material property, and it is affected by the experimental conditions under which it is measured. Therefore, values of γ can differ even by a few orders of magnitude for the same material. In this paper, we demonstrate measurements of hydrogen recombination coefficients at room temperature using an in-house-built catalytic sensor for two selected materials: aluminum Al-5083 (alimex) and stainless steel 316 l, under the load of low-temperature H2 plasma with an admixture of H2O or N2 gases. The plasma settings were carefully chosen to mimic properties of the so-called extreme ultraviolet-generated plasma.1 The measured γ values agree well with literature data obtained for similar plasma conditions and show a correlation with ion energy. Additionally, we show a novel application of the sensor for indirect measurements of the reduction of oxidized surfaces as a function of ion dose. In these experiments, a correlation between reduction time and background water pressure is observed.

Engineering an enzyme-like catalytic sensor for on-site dual-mode evaluation of total antioxidant capacity.

Anovel Fe-MoOx nanozyme, engineered with enhanced peroxidase (POD)-like activity through strategic doping and the creation of oxygen vacancies, is introducedto catalyze the oxidation of TMB with high efficiency. Furthermore, Fe-MoOx is responsive to single electron transfer (SET) and hydrogen atom transfer (HAT) mechanisms related to antioxidants and can serve as a desirable nanozyme for total antioxidant capacity (TAC) determination. The TAC colorimetric platform can reach a low LOD of 0.512μM in solution and 24.316μM in the smartphone-mediated RGB hydrogel (AA as the standard). As proof of concept, the practical application in real samples was explored. The work paves a promising avenue to design diverse nanozymes for visual on-site inspection of food quality.

Hydrogen Sensor with a Thick Catalyst Layer Anchored on Polyimide Film

AbstractHydrogen sensors are important in a hydrogen‐driven society to prevent explosions caused by hydrogen leaks into the atmosphere. In previous studies, resistive hydrogen sensors on polymer films have metal oxide nanostructures decorated with novel metals that enable good responses at room temperature. However, the in situ growth process of sensing nanostructures has the disadvantage of ineffective fabrication, particularly when preparing a thick catalyst layer to produce reliable readouts from the catalytic hydrogen combustion. This work presents a catalytic combustion hydrogen sensor with a thick catalyst layer anchored in a UV resin layer on polyimide film. Catalyst anchoring channels are made by UV imprinting with a glass mold. The sensor consists of a sensing electrode and a microheater, both made of Au within an area of 1.2 mm diameter. UV imprinting produces a UV resin layer of 27 µm thick and catalyst anchoring channels of 14 µm deep and 20–30 µm wide, which are filled with Pt/TiO2 as a catalyst. The sensing response is 7.9% for 1% H2 under ambient conditions, and the detection range is 0.1–3% H2. The UV‐resin microstructures can effectively retain a thick catalyst layer to enhance sensitivity, and their low thermal conductivity reduces heat loss.

Enhanced PtRu by CeO2 hollow nanofibers: Hydrogen gas sensing with CO-resistant in fuel cell

The broad flammability range of hydrogen (4–75 %) underscores the critical need for precise and efficient detection methods. Traditional catalytic combustion sensors can detect combustible gases rapidly; however, they have disadvantages such as high operating temperatures, increased power consumption, and dependence on platinum, with vulnerability to CO poisoning. This study introduced a groundbreaking approach that utilizes CeO₂ hollow nanofibers supported by PtRu nanoparticles to sense hydrogen under extreme conditions, including environments with CO concentrations up to 500 ppm. The unique structure of CeO₂, derived from the Pt/Ce3+ redox pair, provides a high density of oxygen vacancies, which enhances hydrogen detection and enables reactions at room temperature. Our sensor can detect hydrogen concentrations ranging from as low as 100 ppm to as high as 50 %, showcasing its wide detection range and superior selectivity. Our findings confirmed the superior performance of the sensor in realizing consistent and rapid detection in a CO-rich atmosphere. This study presented a significant step toward robust wide-range hydrogen detection, paving the way for safer and more sustainable environmental monitoring.

Tuning multiple enzyme-like activities by metal doping for identification and quantitation of antioxidants in cosmetics

Inspired by the hydrolysis behaviors of skin cells, we exquisitely designed and synthesized a class of hydrolase mimics to develop an analytical method that can both identify and quantity antioxidant components in skin-whitening cosmetics, including ascorbic acid (AA) and its glycoside and phosphate derivatives. A series of ultra-thin Cu1-xMnxO2 or Fe1-yMnyO2 with rich acid-base pairs were prepared via chemical deposition and in-situ CuI/FeII self-assembly. H218O and D216O isotopic labeling studies and density function theory (DFT) calculations were adopted to analyze the cleaving sites of ascorbyl phosphate (AAL)/ascorbyl glucoside (AAP) and confirm that H2O was involved in the new bonds. In-situ DRIFT NH3-IR and −TPD further confirmed that the Fe- or Cu-substitution could increase the quantity and strength of Brønsted and Lewis acid sites. A cascade catalytic fluorescence sensor was designed for selective recognition or quantification of AA and its derivatives, which presents ultra-high-precision (≤2.5 %), stability, and selectivity in testing the target ingredients of five cosmetics from the market. Our nanozymes exhibit higher catalytic efficiency of 17.1 s−1 for AA, 8.42 s−1 for AAL, and 3.32 s−1 for AAP, which are 5.6 ∼ 32.8-fold higher than those of their mimic proteases. This work provides a controllable methodology to design hydrolytic nanozymes, which sheds light on biomimetic engineering and paves the way for breakthroughs in cosmetics industrial applications in the future.

Catalytic NIR chemiluminescence sensor with enhanced persistence and intensity for in vivo imaging

Chemiluminescence (CL) is a self-illumination phenomenon that involves the emission of light from chemical reactions, and it provides favorable spatial and temporal information on biological processes. However, it is still a great challenge to construct effective CL sensors that equip strong CL intensity, long emission wavelength, and persistent luminescence for deep tissue imaging. Here, we report a liposome encapsulated polymer dots (Pdots)-based system using catalytic CL substrates (L-012) as energy donor and fluorescent polymers and dyes (NIR 695) as energy acceptors for efficient Near-infrared (NIR) CL in vivo imaging. Thanks to the modulation of paired donor and acceptor distance and the slow diffusion of biomarker by liposome, the Pdots show a NIR emission wavelength (λ em, max = 720 nm), long CL duration (>24 h), and a high chemiluminescence resonance energy transfer efficiency (46.5 %). Furthermore, the liposome encapsulated Pdots possess excellent biocompatibility, sensitive response to H2O2, and persistent whole-body NIR CL imaging in the drug-induced inflammation and the peritoneal metastatic tumor mouse model. In a word, this NIR-II CL nanoplatform with long-lasting emission and high spatial-temporal resolution will be a concise strategy in deep tissue imaging and clinical diagnostics.

Co3O4-Based Materials as Potential Catalysts for Methane Detection in Catalytic Gas Sensors.

The present work deals with the development of Co3O4-based catalysts for potential application in catalytic gas sensors for methane (CH4) detection. Among the transition-metal oxide catalysts, Co3O4 exhibits the highest activity in catalytic combustion. Doping Co3O4 with another metal can further improve its catalytic performance. Despite their promising properties, Co3O4 materials have rarely been tested for use in catalytic gas sensors. In our study, the influence of catalyst morphology and Ni doping on the catalytic activity and thermal stability of Co3O4-based catalysts was analyzed by differential calorimetry by measuring the thermal response to 1% CH4. The morphology of two Co3O4 catalysts and two NixCo3-xO4 with a Ni:Co molar ratio of 1:2 and 1:5 was studied using scanning transmission electron microscopy and energy dispersive X-ray analysis. The catalysts were synthesized by (co)precipitation with KOH solution. The investigations showed that Ni doping can improve the catalytic activity of Co3O4 catalysts. The thermal response of Ni-doped catalysts was increased by more than 20% at 400 °C and 450 °C compared to one of the studied Co3O4 oxides. However, the thermal response of the other Co3O4 was even higher than that of NixCo3-xO4 catalysts (8% at 400 °C). Furthermore, the modification of Co3O4 with Ni simultaneously brings stability problems at higher operating temperatures (≥400 °C) due to the observed inhomogeneous Ni distribution in the structure of NixCo3-xO4. In particular, the NixCo3-xO4 with high Ni content (Ni:Co ratio 1:2) showed apparent NiO separation and thus a strong decrease in thermal response of 8% after 24 h of heat treatment at 400 °C. The reaction of the Co3O4 catalysts remained quite stable. Therefore, controlling the structure and morphology of Co3O4 achieved more promising results, demonstrating its applicability as a catalyst for gas sensing.

Catalytic thermoelectric hydrogen sensor with CoSb3 thermopile by single-step deposition on bare/textured glass

Hydrogen sensors are required due to the flammability of hydrogen in air. Catalytic thermoelectric hydrogen sensors show promise because they provide direct voltage output from a temperature difference generated by the catalytic combustion of hydrogen. CoSb3 is a good thermoelectric material for energy harvesting and sensing. However, conventional CoSb3 thermopiles require the separate deposition of p- and n-type thermoelectric elements. This study proposes the surface roughness modification of a soda-lime glass substrate through the development of a textured glass surface to prepare a CoSb3 thermopile by single-step deposition. A Co-In-Sb stack with a SiO2 capping layer is deposited by an e-beam evaporator on bare/textured glass and thermally activated under room conditions, which produces a thermoelectric pair due to the partial release of volatile Sb from cracks developed in the rough layer formed on textured glass. A thermoelectric pair consists of a CoSb3 layer with a deficiency of Sb (n-type) on textured glass and that with an excess of Sb (p-type) on bare glass. A hydrogen sensor is made with CoSb3 thermopile with 41 thermoelectric pairs and a catalyst reservoir coated with hydrogen oxidation catalyst. The sensor shows a sensitivity of 13 mV for 1 % H2 in air at room temperature.

Highly sensitive SERS sensors for glucose detection based on enzyme@MOFs and ratiometric Raman

Diabetes is a common chronic metabolic disease. The frequent fluctuation of glucose is the main cause of most diabetes complications, which in turn causes harm to the health of patients. Surface-enhanced Raman scattering (SERS) spectroscopy has attracted much attention in the rapid detection of glucose due to its unique molecular fingerprinting ability, ultra-high sensitivity and fast response. However, due to the low affinity between glucose and SERS substrate, poor signal, susceptibility to complex environmental interference, and poor stability of SERS detection, it is still a challenge for SERS to accurately and sensitively determine glucose in complex environments. In this work, we encapsulated 4-mercaptobutyronitrile (4-MBN) as an internal standard (IS) in Au@Ag NRs inside and then Au@4-MBN@Ag NRs, Leucomalachite Green (LMG), glucose oxidase (GOx) and horseradish peroxidase (HPR) were encapsulated in ZIF-8 to prepare a tandem enzyme catalytic ratiometric SERS sensor Au@4-MBN@Ag@LMG@ZIF-8(GOx, HPR) for the detection of glucose in saliva. Because ZIF-8 enhanced the catalytic activity of the enzyme, the ability of glucose enrichment, and weakens the aggregation of Ag NRs. The internal standard signal molecule improves the accuracy and sensitivity of detection. The ratiometric Raman signal I412/I2233 of glucose has a good linear relationship with the concentration in the range of 0.1–100 μM, and the limit of detection (LOD) could be down to 0.03 μM. At the same time, it has excellent selectivity, repeatability and accuracy. The recovery rate of glucose in saliva is 96.50%–105.56 %, which proves the feasibility of the method. The Au@4-MBN@Ag@LMG@ZIF-8(GOx, HPR) sensor prepared in this study showed excellent SERS performance, which was able to detect glucose quickly, sensitively and accurately. This work provides a new strategy for the design of enzyme-catalyzed SERS sensors.

High performance microheater-based catalytic hydrogen sensors fabricated on porous anodic alumina substrates

Catalytic combustion-type gas sensors are widely used in industry and everyday life for detecting flammable gases. However, high power consumption is one of the main drawbacks of the catalytic sensors. Replacing the platinum wire heating element with a thin-film microheater can significantly reduce power consumption, but maintaining high sensitivity and long-term stability of such devices is a challenge. Here we developed microheater-type catalytic hydrogen sensors based on porous anodic aluminium oxide served simultaneously as a substrate for platinum microheater and as a carrier for a catalyst. The fabricated sensors have a high sensitivity of 76 mV/vol% hydrogen. The deviation of the sensor response during continuous operation for 14 days is less than 4%. The relative humidity of the ambient atmosphere does not affect the sensor response. The fast sensor response time (0.4 s) makes it possible to use the pulsed power supply mode to reduce the power consumption to 3.2 mW without sacrificing the measurement accuracy. The performance of the developed catalytic hydrogen sensors promotes the high competitiveness in the market and the prospects for industrial applications.

Functionalization of three-dimensional epitaxial graphene with metal nanoparticles.

We demonstrate the first successful functionalization of epitaxial three-dimensional graphene with metal nanoparticles. The functionalization is obtained by immersing three-dimensional graphene in a nanoparticle colloidal solution. This method is versatile and demonstrated here for gold and palladium, but can be extended to other types of nanoparticles. We have measured the nanoparticle density on the top surface and in the porous layer volume by scanning electron microscopy and scanning transmission electron microscopy. The samples exhibit a wide coverage of nanoparticles with minimal clustering. We demonstrate that high-quality graphene promotes the functionalization, leading to higher nanoparticle density both on the surface and in the pores. X-ray photoelectron spectroscopy shows the absence of contamination after the functionalization process. Moreover, it confirms the thermal stability of the Au- and Pd-functionalized three-dimensional graphene up to 530 °C. Our approach opens new avenues for utilizing three-dimensional graphene as a versatile platform for catalytic applications, sensors, and energy storage and conversion.

3-D Nanostructure Palladium Synthesis By Electrochemical Deposition for Hydrogen Sensor with Switching Resistance Characteristic in Normal Temperature and Pressure

In the hydrogen industry, it is crucial to detect hydrogen leaks and monitor its concentration due to its highly explosive, flammable, and diffusive properties in the concentration range of 4%-75%. Until now, hydrogen sensors have been focused on oxide materials at high temperature and pressure conditions such as semiconductor and steel processes. However, in the future of the hydrogen industry, it is important to sense hydrogen at normal temperature and pressure (NTP). To develop hydrogen sensors with fast response time and high sensitivity specifically designed for NTP conditions, various material properties and structural aspects such as film, nanostructure, and multilayer are being experimentally explored.Metal resistance hydrogen sensors utilize changes in resistance due to hydrogen adsorption and absorption. Compared to other sensors such as catalytic and thermal conductivity sensors, metal resistance hydrogen sensors have advantages such as excellent sensitivity, response time, and selectivity. Palladium metal exhibits superior characteristics with regard to hydrogen compared to other metals, due to its low activation energy for hydrogen molecule dissociation reaction and high reactivity in absorbing hydrogen at NTP.[1] Also, palladium with 3-D nanostructures exhibits a switching resistance characteristic, where the resistance initially decreases rapidly and then increases because of hydrogen and palladium reaction.[2] This depends on the hydrogen concentration and exposure time, which is due to a phenomenon where the combined effects of characteristics such as hydrogen interstitial, phase transition, and volume expansion lead to different responses of hydrogen and palladium.In this study, we focused on the resistance switching characteristic of palladium, specifically its response to changes in hydrogen concentration and exposure time. We used this characteristic to experiment with both the material and structural properties of palladium nanostructures. We varied impurities and additives in the palladium electrodeposition solution to control the material properties, and varied parameters such as concentration, pH, and voltage using electrochemical methods for structural properties. Structural and material properties were analyzed using Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS), and X-ray Photoelectron Spectroscopy (XPS). Sensing characteristics were then analyzed using a hand-made sensor platform with a Source Meter.[Reference][1] Dekura, S., Kobayashi, H., Kusada, K., & Kitagawa, H. (2019). Hydrogen in Palladium and Storage Properties of Related Nanomaterials: Size, Shape, Alloying, and Metal‐Organic Framework Coating Effects. ChemPhysChem, 20(10), 1158-1176.[2] Cho, S. Y., Ahn, H., Park, K., Choi, J., Kang, H., & Jung, H. T. (2018). Ultrasmall grained Pd nanopattern H2 sensor. ACS sensors, 3(9), 1876-1883.

Response of Catalytic Hydrogen Sensors at Low and Negative Ambient Temperatures

Response of Catalytic Hydrogen Sensors at Low and Negative Ambient Temperatures

UiO-66-NH2-PEI combined with a hand-held catalytic combustion sensor for trace acetone detection in exhaled breath

The trace acetone determination in breath can be regarded as a noninvasive method for diagnostic of diabetes. There is an urgent demand to develop a simple method for acetone detection which can be easily performed at home. Here, UiO-66-NH2@PEI with the appropriate aperture size combined with the hand-held sensor was used to construct the adsorption–desorption sensing platform for separation and enrichment of acetone in exhaled breath (EB). UiO-66-NH2@PEI can realize the selective adsorption, desorption and separation for acetone in EB. The flameless combustion hand-held sensor can sensitively respond to acetone in the range of 0.2–12.0 ppm and it can achieve the accurate determination of acetone content in EB of diabetic patients. The hand-held sensor is inexpensive, lightweight and easy to operate, which has great application prospects for the widespread use for diabetic patients in family life.

Hydrogen sensor with a thick catalyst layer anchored on soda-lime glass

Hydrogen is a green energy source with zero pollutant emissions and increasing demand. Hydrogen sensors are required due to the flammable nature of hydrogen in air. Current catalytic combustion hydrogen sensors based on membrane platforms strike a balance between sensitivity and mechanical strength. A thick catalyst layer allows enhanced sensor sensitivity, producing an acceptable sensor signal change. A hydrogen sensor with a thick catalyst layer is introduced on soda-lime glass, which has low thermal conductivity and prefabricated catalyst anchoring channels. The hydrogen sensor is composed of a 44 Ω platinum sensing electrode and a 100 Ω gold microheater, both of which are coated with a thin layer of alumina. The sensing electrode is buried in the catalyst anchoring channels with a 10 μm depth and 78 μm width using a hydrogen combustible catalyst. The response for 1 % H2 in air is 9.43 % in a test chamber at 80 °C with a response time of 48 s and recovery time of 75 s. The calculated temperature increment due to catalytic combustion is 84 °C. A hydrogen sensor with a thick catalyst layer on soda-lime glass shows enhanced heat generation, resulting in an improved thermoresistive response, and consistent mechanical support.