SnO2 submicron porous cube derived from metal-organic framework for n-butanol sensing at room temperature

SnO₂ is a typical metal oxide semiconductor gas sensitive material, which has been studied deeply. However, pure SnO₂ sensing materials usually have good performance at high operating temperatures. In this study, we reported an n-butanol sensor with high selectivity and fast response based on SnO₂ submicron porous cube prepared by heating and decomposing the Sn-based metal-organic framework material (Sn-MOF) in air at a certain temperature. SnO₂ submicron porous cube prepared at 450 °C shows good response and selectivity for n-butanol. And it has a response (%) of 175% to 100 ppm n-butanol and a relatively fast response/recovery time of 184 s/183 s at room temperature. The (110) crystal plane with sufficient oxygen-rich vacancy can adsorb O₂ and n-butanol molecules more effectively. Therefore, its sensitivity to n-butanol gas can be significantly improved. This work provides a good idea for further research on pure metal oxide semiconductor room temperature gas sensors.     

Electroless plated SnO2–Pd–Au composite thin film for room temperature H2 detection

Extremely thin SnO₂ nanosheets with high surface area were fabricated through a one-pot hydrothermal method. In this work, gas sensing property of the SnO₂ nanosheets was studied. SnO₂–Pd–Au mixed thin films were prepared by electroless deposition of Pd, Au, and nanostructured SnO₂ onto the surface of a high resistance alumina substrate. The whole fabrication process was carried out at room temperature without any thermal treatment required. The films deposited on the alumina substrate were characterized by SEM and EDS. The co-deposited Au improved the electric conductance of the sensing film. A relatively large amount of Pd (Pd/Sn ratio around 1:1) was obtained for the film instead of the usually low doping value of Pd (∼0.1% level) for SnO₂ hydrogen sensor. It has been found that the SnO₂–Pd–Au composite film sensor has fast response in the range of 134–1469 ppm toward hydrogen gas at room temperature. The sensor also shows good stability and repeatability. Effects of annealing condition of the sensing film on H₂ gas sensing performance was investigated as well. A possible machnism for SnO₂–Pd room temperature hydrogen sensing is proposed.     

Semi shield driven p-n heterostructures and their role in enhancing the room temperature ethanol gas sensing performance of NiO/SnO2 nanocomposites

The demand for the development of gas sensors operable at room temperature is increasing due to the uncountable drawbacks of high temperature gas sensors. This contribution describes the fabrication of room temperature ethanol sensor. The synthesis of NiO semi shielded SnO₂ (NiO/SnO₂) nanocomposites (NCs) was done via a simple two-step process, started with co-precipitation technique and then followed by sol-gel method. High resolution electron microscope (HRTEM) results indicated the semi shielding of NiO on SnO₂ nanoparticles (NPs). Surface morphological studies of the fabricated sensors show the porous nature of the samples which further helps in enhanced sensing response. X-ray photoelectron spectroscope (XPS) results of NiO/SnO₂ NCs revealed the valence states of Ni (+2) and Sn (+4). Excellent gas sensing response of the NiO/SnO₂ sensor towards ethanol at room temperature was observed from the gas sensing studies. The response of NiO/SnO₂ (∼140) was nearly 9 times higher than SnO₂ sensor (∼15) and nearly 11 times higher than NiO sensor (12.98) towards 100 ppm ethanol at room temperature. The observed response and recovery times of NiO/SnO₂ were 23 s and 13 s respectively. The p-n heterostructure formed between p-NiO and n-SnO₂, and high chemical sensitization and catalytic activity of the NiO are the main contributors for the excellent sensing performance of NiO/SnO₂ sensor.     

Heterostructure nanoarchitectonics with ZnO/SnO2 for ultrafast and selective detection of CO gas at low ppm levels

Heterojunction-based gas sensors are very attractive as they substantially improve the sensing characteristics due to the effective potential barrier present at the interface. Taking the advantages of two excellent semiconducting gas sensing materials i.e., SnO₂ and ZnO, herein, we have constructed ZnO/SnO₂ heterojunction by the combination of vacuum evaporation and r.f. sputtering or atomic layer deposition techniques. The ZnO/SnO₂ heterostructure with optimized thickness of ZnO (～10 nm) shows a 6-fold enhancement in sensing response compared to bare SnO₂ films against CO gas. The sensing responses of 81 and 85 % have been obtained for ZnO/SnO₂ heterostructures with ZnO deposited by sputtering and atomic layer deposition (ALD) methods, respectively, against 91 ppm of CO gas with an estimated limit of detection of 1.67 and 0.37 ppm. The ALD ZnO/SnO₂ sample displays an extremely fast response time of 5 s. The heterostructure sensors are also highly selective towards CO gas in the presence of other interfering toxic agents. The enhanced sensing characteristics of ZnO/SnO₂ are assigned to the formation of n-n heterojunction as depicted by X-ray photoelectron spectroscopic band alignment study and the strong CO adsorption on ZnO surface as derived from density functional theory calculations.     

Band-gap-tunable CeO2 nanoparticles for room-temperature NH3 gas sensors

NH₃ is a type of essential raw material but harmful. In this work, CeO₂ nanoparticles were synthesized as NH₃ gas sensing materials by simple hydrothermal method. The response time of the sensor is extremely fast (3 s) towards 500 ppm NH₃ with the response of 22.0 at room temperature. The concentration of NH₃ and its response show well-matched functional relationship in the range of 0.5 ppm-1000 ppm. The selectivity of NH₃ is distinct and the detection limit is as low as 500 ppb. The excellent NH₃ gas sensing performance may be attributed to more oxygen vacancies and narrower band gap. This CeO₂ nanoparticles-based gas sensor could be reliable to detect and monitor NH₃ at room temperature.     

Highly sensitive gas sensors on low-cost nanostructured polymer substrates

SnO₂ thin-film gas sensors have been successfully fabricated on nanospiked polyurethane polymer surfaces, which are replicated by a low-cost soft nanolithography method from silicon nanospike structures formed with femtosecond laser irradiations. Measurements revealed significant response to carbon monoxide (CO) gas at room temperature, which is considerably different from the sensors of SnO₂ thin films coated on smooth surfaces that show no response to CO gas at room temperature. The high area/volume ratio and sharp structures of the nanospikes enhance the sensitivity of SnO₂ at room temperature. This will greatly decrease the electrical power consumption of the gas sensor and the cost for calibrations, and has great potential for application in other sensing systems.     

Bias dependent NO2 sensitivity of SnO2 thin films at room temperature

Amorphous granular SnO₂ thin films were investigated from a standpoint of an NO₂ gas sensor working at room temperature. The films were deposited using pulsed laser deposition method with substrate at room temperature and ～90 nm thick SnO₂ films with amorphous structure were obtained as a result. SnO₂ films deposited on Pt electrode substrates formed a sensor structure that showed response I_air/I_gas to 4 ppm NO₂ up to ～8000. I–V characteristics of the sensor structure were described by the power law dependence, whereas the power indexes were different for measurements in pure air and in the presence of NO₂. As a result, the sensor response was highly dependent on bias voltage between the sensor electrodes. It was demonstrated that the nonlinear electrical characteristics and bias dependent gas sensitivity were the inherent properties of thin films and the contacts were ohmic.     

Enhanced response of the photoactive gas sensor on formaldehyde using porous SnO2@TiO2 heterostructure driven by gas-flow thermal evaporation and atomic layer deposition

Nanoporous SnO₂@TiO₂ heterostructure was synthesized by a facile two-step dry process, modified thermal evaporation followed by atomic layer deposition (ALD). The introduction of inert gas, Ar, with a pressure of 0.2 Torr during thermal evaporation of SnO, enabled the formation of the nanoporous 3D structure by inducing the collision and loss of kinetic energy during deposition. A photocatalytic material, TiO₂, was grown on the porous structure of SnO₂ to detect target gas, formaldehyde, under UV irradiation selectively. Microstructural and elemental analysis with a transmission electron microscope and X-ray photoelectron spectroscopy confirmed the porous structure of SnO₂ induced by our evaporation process as well as the conformal coating of TiO₂ on the porous structure. The sensing capabilities of a photoactive sensor on the formaldehyde were assessed in terms of the film porosity, irradiated UV power, and thickness of photoactive materials at room temperature. As a result, the SnO₂@TiO₂ heterostructure, with an optimum thickness of TiO₂ exhibited low detection limit, down to 0.1 ppm, good linearity to the concentration of formaldehyde in the range of 0.1–10 ppm, and high response of 15% in the HCHO 0.1 ppm. This core-shell porous structure developed by modified thermal evaporation combined with ALD paved the way for 3D architectures to explore various applications, such as biosensors, photocatalysts, and optoelectronic devices.     

Improved ethanediol sensing with single Yb ions doped SnO2 nanobelt

Yb-doped SnO₂ nanobelts (Yb–SnO₂ NBs) and pure SnO₂ nanobelts (SnO₂ NBs) are successfully synthesized by thermal evaporation method and their composition and morphology are characterized. The single nanobelt device is fabricated by dual-ion beam deposition system, and the gas sensing performance to ethanediol, methanal, ethanol and acetone is investigated. The results show that the best working temperature of single Yb–SnO₂ NB sensor to ethanediol is 190 °C, which is lower than that of pure counterpart and the highest sensitivity is 10.5 to 100 ppm of ethanediol. In addition, it is found that the response/recovery time is short and the sensor exhibits excellent selectivity and stability. The sensing performance of SnO₂ NB is actually improved by Yb.     

Preparation of hollow SnO2/ZnO cubes for the high-performance detection of VOCs

Detecting volatile organic compounds is essential to improving the environment and human health. This study prepared a novel composite of hollow SnO₂/ZnO cubes using a self-template hydrothermal method followed by a calcination process. The morphology and structure of the composites were characterized using a series of analysis techniques, and the formation mechanism of a hollow cube-like structure was explored. Compared to the hollow SnO₂ cube sensor, the hollow SnO₂/ZnO cube sensor exhibited a strong response (148–100 ppm formaldehyde), fast response/recovery time (15 s/25 s), good linearity (R² = 0.995), good repeatability, and excellent stability. The superior gas sensing property of the hollow SnO₂/ZnO cubes was attributed to the combined advantages of hollow structures and heterojunctions.     

High performance H2 sensor based on rGO-wrapped SnO2–Pd porous hollow spheres

Hydrogen (H₂) sensors based on metal oxide semiconductors (MOS) are promising for many applications such as a rocket propellant, industrial gas and the safety of storage. However, poor selectivity at low analyte concentrations, and independent response on high humidity limit the practical applications. Herein, we designed rGO-wrapped SnO₂–Pd porous hollow spheres composite (SnO₂–Pd@rGO) for high performance H₂ sensor. The porous hollow structure was from the carbon sphere template. The rGO wrapping was via self-assembly of GO on SnO₂-based spheres with subsequent thermal reduction in H₂ ambient. This sensor exhibited excellently selective H₂ sensing performances at 390 °C, linear response over a broad concentration range (0.1–1000 ppm) with recovery time of only 3 s, a high response of ～8 to 0.1 ppm H₂ in a minute, and acceptable stability under high humidity conditions (e. g. 80%). The calculated detection limit of 16.5 ppb opened up the possibility of trace H₂ monitoring. Furthermore, this sensor demonstrated certain response to H₂ at the minimum concentration of 50 ppm at 130 °C. These performances mainly benefited from the special hollow porous structure with abundant heterojunctions, the catalysis of the doped-PdO_x, the relative hydrophobic surface from rGO, and the deoxygenation after H₂ reduction.     

Synthesis and high sensing properties of a single Pd-doped SnO2 nanoribbon

Monocrystal SnO₂ and Pd-SnO₂ nanoribbons have been successfully synthesized by thermal evaporation, and novel ethanol sensors based on a single Pd-SnO₂ nanoribbon and a single SnO₂ nanoribbon were fabricated. The sensing properties of SnO₂ nanoribbon (SnO₂ NB) and Pd-doped SnO₂ nanoribbon (Pd-SnO₂ NB) sensors were investigated. The results indicated that the SnO₂ NB showed a high sensitivity to ethanol and the Pd-SnO₂ NB has a much higher sensitivity of 4.3 at 1,000 ppm of ethanol at 230°C, which is the highest sensitivity for a SnO₂-based NB. Pd-SnO₂ NB can detect ethanol in a wide range of concentration (1 ~ 1,000 ppm) with a relatively quick response (recovery) time of 8 s (9 s) at a temperature from 100°C to 300°C. In the meantime, the sensing capabilities of the Pd-SnO₂ NB under 1 ppm of ethanol at 230°C will help to promote the sensitivity of a single nanoribbon sensor. Excellent performances of such a sensor make it a promising candidate for a device design toward ever-shrinking dimensions because a single nanoribbon device is easily integrated in the electronic devices.     

Tin–Zinc oxide composite ceramics for selective CO sensing

Composite metal oxide gas sensors were intensely studied over the past years having superior performance over their individual oxide components in detecting hazardous gases. A series of pellets with variable amounts of SnO₂ (0–50 mol%) was prepared using wet homogenization of the component oxides leading to the composite tin-zinc ceramic system formation. The annealing temperature was set to 1100 °C. The samples containing 2.5 mol% SnO₂ and 50 mol% SnO₂ were annealed also at 1300 °C, in order to observe/to investigate the influence of the sintering behaviour on CO detection. The sensor materials were morphologically characterized by scanning electron microscopy (SEM). The increase in the SnO₂ amount in the composite ceramic system leads to higher sample porosity and an improved sensitivity to CO. It was found that SnO₂ (50 mol%) - ZnO (50 mol%) sample exhibits excellent sensing response, at a working temperature of 500 °C, for 5 ppm of CO, with a fast response time of approximately 60 s and an average recovery time of 15 min. Sensor selectivity was tested using cross-response to CO, methane and propane. The results indicated that the SnO₂ (50 mol%)-ZnO (50 mol%) ceramic compound may be used for selective CO sensing applications.     

Highly sensitive acetone sensor based on Eu-doped SnO2 electrospun nanofibers

In this study, a series of undoped and Eu-doped SnO₂ nanofibers were synthesized via a simple electrospinning technique and subsequent calcination treatment. Field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) were carefully used to characterize the morphologies, structures and chemical compositions of these samples. The results reveal that the as-prepared nanofibers are composed of crystallite grains with an average size of about 10 nm and Eu³⁺ ions are successfully doped into the SnO₂ lattice. Compared with pure SnO₂ nanofibers, Eu-doped SnO₂ nanofibers demonstrate significantly enhanced sensing characteristics (e.g., large response value, short response/recovery time and outstanding selectivity) toward acetone vapor, especially, the optimal sensor based on 2 mol% Eu-doped SnO₂ nanofibers shows the highest response (32.2 for 100 ppm), which is two times higher than that of the pure SnO₂ sensor at an operating temperature of 280 °C. In addition, the sensor exhibits a good sensitivity to acetone in sub-ppm concentrations and the detection limit could extend down to 0.3 ppm, making it a potential candidate for the breath diagnosis of diabetes.     

LaNiTiO3-SE-based stabilized zirconium oxide mixed potentiometric SO2 gas sensor

In this paper, a mixed potential gas sensor based on YSZ solid electrolyte and LaNiTiO₃ sensing electrode was produced. The perovskite-type oxide LaNiTiO₃ was synthesized by the sol-gel method as a sensitive electrode, which was intended to detect the low-level concentration of SO₂ in the environment. After the aging process and continuous testing, it was found that the LaNiTiO₃-SE sensor had the best response value of ?27.5 mV to 5 ppm SO₂ at 510 °C, at this temperature, as low as 50 ppb SO2 still had a response of -1mV. Meanwhile, when the sensor was tested at 510 °C, it was found that the response value of the sensor showed a piecewise linear relationship with the logarithm of SO₂ concentration, with a sensitivity of -4 mV/decade for 0.05–1 ppm SO₂ and -40mV/decade for 1–100 ppm SO₂. In addition, the sensor also showed good selectivity, and the response to interference gases could be ignored such as NO₂, CO, CH₄, NH₃, H₂, ethanol, and formaldehyde. At the same time, the sensor also shows good repeatability and stability, being still relatively stable after two weeks of continuous operation at high-temperature.     

Nanostructured SnO2 thin films for NO2 gas sensing applications

We report the synthesis of nanostructured SnO₂ by a simple inexpensive sol–gel spin coating method using m-cresol as a solvent. This method facilitates rapid synthesis at comparatively lower temperature enabling formation of nanostructures suitable for gas-sensing applications. Various physicochemical techniques have been used for the characterization of SnO₂ thin films. X-ray diffraction analysis confirmed the single-phase formation of tetragonal SnO₂ having crystallite size 5–10 nm. SnO₂ showed highest response (19%) with 77.90% stability toward 100 ppm nitrogen dioxide (NO₂) at 200 °C. The response time of 7 s and recovery time of 20 min were also observed with the same operating parameters. The probable mechanism is proposed to explain the selective response toward nitrogen dioxide. Impedance spectroscopy studies showed that the response to nitrogen dioxide is mainly contributed by grain boundaries. The reproducibility and stability study of SnO₂ sensor confirmed its candidature for detection of NO₂ gas at low concentration (10–100 ppm) and lower operating temperature.     

SiC Foams Decorated with SnO2 Nanostructures for Room Temperature Gas Sensing

Cell walls of the commercial silicon carbide (SiC)‐based foams were decorated by one‐dimensional tin dioxide (SnO₂) nanostructures. Thermal evaporation of SnO₂ powder with the assistance of a Au catalyst in inert atmosphere caused the formation of SnO₂ nanobelts on the pore surfaces. The room temperature (RT) ammonia (NH₃) and nitrogen dioxide (NO₂) gas sensing behaviors were investigated systematically in both dry and humid air atmosphere with/without UV activation. The results were compared to those for bare SnO₂ and SiC. It was shown that SiC/SnO₂ composite was efficient to detect low concentration of NH₃ (10–50 ppm) and NO₂ (1–5 ppm) under humid air and UV activation at RT.     

Nanocrystalline In2O3-SnO2 thick films for low-temperature hydrogen sulfide detection

Nanocrystalline In₂O₃-SnO₂ thick films were fabricated using the screen-printing technique and their responses toward low concentrations of H₂S in air (2-150 ppm) were tested at 28-150 °C. The amount of In₂O₃-loading was varied from 0 to 9 wt.% of SnO₂ and superb sensing performance was observed for the sensor loaded with 7 wt.% In₂O₃, which might be attributed to the decreased crystallite size as well as porous microstructure caused by the addition of In₂O₃ to SnO₂ without structural modification. The interfacial barriers between In₂O₃ and SnO₂ might be another major factor. Typically, the response of 7 wt.% In₂O₃-loaded SnO₂ sensor toward 100 ppm of H₂S was 1481 at room temperature and 1921 at optimal operating temperature (40 °C) respectively, and showed fast and recoverable response with good reproducibility when operated at 70 °C, which are highly attractive for the practical application in low-temperature H₂S detection.     

Realization of low-temperature and selective NO2 sensing of SnO2 nanowires via synergistic effects of Pt decoration and Bi2O3 branching

Metal oxide semiconductors with branched structures, such as branched nanowires (b-NWs), have promising properties for being used in gas sensors. In this work, we synthesized Pt-decorated Bi₂O₃-branched SnO₂ nanowires (NWs). NO₂ sensing studies revealed the superior capacity of a Pt-decorated Bi₂O₃-branched SnO₂ NWs gas sensor relative to pristine and branched SnO₂ gas sensors, and it worked at near room temperature (50 °C). The increased sensing capacity was related to the synergistic effects of Pt decoration and Bi₂O₃ branching, particularly the morphology of the gas sensor with branched structures, the promising effects of Pt as a noble metal with good catalytic activity, and the generation of homo- and heterojunctions in the Pt-decorated Bi₂O₃-branched SnO₂ NWs gas sensor. The results obtained in this work are useful for design and development of NO₂ gas sensors using a simple strategy, which can be easily extended to various metal oxides.     

Investigation on microstructure and nonanal sensing properties of hierarchical Sb2WO6 microspheres

Various metal oxides with unique microstructures have been hopeful in fabricating gas sensors applications. This paper reports the room-temperature sensing properties of hierarchical Sb₂WO₆ (antimony tungstate) microspheres for nonanal, which is a dominant aromatic aldehyde compound in cooked rice. The hierarchical Sb₂WO₆ microspheres were obtained by pH control (from pH 1 to 5) through a one-step hydrothermal reaction. The experiment indicated that the optimal response of the Sb₂WO₆ (pH = 4) gas sensor to 30 ppm nonanal reached 62 at room temperature, which was about 8 times that of Sb₂WO₆ (pH = 1). The improved sensing performance resulted from the finer microstructure and larger specific surface area of Sb₂WO₆ with a pH value of 4, providing abundant adsorption sites for nonanal molecules. Meanwhile, the practicability of cooked rice stored for various periods was verified through gas detection, and the results indicated that the sensor might recognize the deterioration of cooked rice and ready-to-eat rice. Therefore, the as-prepared sensor can be used in electronic nose systems to detect cooked rice and ready-to-eat rice deterioration and improve rice cooking methods.