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In this study, reduced graphene oxide (RGO) nanosheets were synthesized and then functionalized with Pt nanoparticles (NPs) for gas sensing studies at room temperature. Pt-functionalized RGOs (Pt-RGOs) were irradiated by a 2 MeV electron beam with different doses of 100 and 500 kGy (Pt-RGO-100 and Pt-RGO-500) to study the role of electron beam irradiation (EBI) on properties and NO2 gas sensing characteristics. Different characterization techniques verified the generation of structural defects after EBI. Additionally, NO2 sensing tests at room temperature revealed that the Pt-RGO-100 sensor had the highest response to NO2 gas as well as the shortest response time. We surmise that the improved sensing signal with respect to NO2 gas for Pt-RGO-100 sensor was related to the role of oxygen functional groups. However, decreases in the response for Pt-RGO-500 sensor were related to the creation of reactive oxygen gases that could be adsorbed on the active defects of the RGO by the interaction of electron beams with oxygen species in the ambient air, leading to a decrease of the effective defect sites and decreases of the sensing response. This work suggests progress towards an improved performance of RGO-based gas sensors that can work at low temperature, by using EBI as a clean tool applied at room temperature with Pt-functionalization.

Assuming that many of the materials produced in a non-equilibrium state remain unchanged, an extended space-energy conservation law was proposed based on the existing energy conservation law. In the present study, by analyzing the well developed equilibrium binary phase diagram of iron (Fe) - carbon (C), we show that energy non-equilibrium microstructures can appear as a part of the equilibrium between the space energy and the mass energy. The correlation between these two energies is objectively and logically explained via (1) one-to-one correspondences between the equilibrium and non-equilibrium phases based on the binary Fe-C phase diagram and (2) the heat-treated Fe-C phases with the spatial energy represented by temperature. Additionally, we found that the morphological and microstructural changes in non-equilibrium states could be consistently explained using the extended energy law as a major premise. This suggests that material factors such as size, distribution, and the shape of materials, which appear to have no energy transfer, are all formed to balance the energy equilibrium with the spatial energy surrounding the materials. Thus, an extended energy conservation law, which can control mass through space or vice versa, can provide a comprehensive logical framework for analyzing various unsolved physicochemical phenomena. (Received May 28, 2020; Accepted June 17, 2020)

In this work, a low-temperature (100 °C) gas sensor based on heterojunctions of porous Si and SnO2 nanowires (NWs) is presented. Porous Si was obtained from p-Si wafers by electrochemical etching, and SnO2 NWs were fabricated by a vapor-liquid-solid route. Different characterization techniques were used to verify the formation of porous Si/SnO2 NW heterojunctions. H2S gas sensing results showed enhanced gas sensing performance of the porous Si/SnO2 NW sensor in comparison with that of a porous Si sensor. The reasons for such enhancement are discussed in detail. This study demonstrates the promising effects of SnO2 NWs in combination with porous Si to realize low-temperature H2S gas sensors that are highly compatible with existing Si processing technology.

A new gas sensor working in room temperature, which is compatible with silicon fabrication technology is presented. Porous silicon nanowires (NWs) were synthesized by metal-assisted chemical etching method and then TeO₂ NWs branches were attached to their stem by thermal evaporation of Te powders in the presence of air. Afterwards TeO₂ branched porous Si NWs were functionalized by Pt via sputtering followed by low temperature thermal annealing. Scanning electron microscopy, transmission electron microscopy and energy-dispersive X-ray spectroscopy collectively confirmed successful formation of TeO₂ branched porous Si NWs functionalized by Pt nanoparticles. Their gas sensing properties in the presence of CO, C6H6 and C7H8 were tested at room temperature, for Si wafer, pristine porous Si NWs, pristine TeO₂ branched porous Si NWs, and Pt functionalized TeO₂ branched porous Si NWs sensors. Pt functionalized TeO₂ branched porous Si NWs have higher responses to all tested gases than the other sensors. The origin of high response is discussed in detail. This new room temperature gas sensor can open a new aperture for development of gas sensors with minimum energy consumption which are compatible with silicon fabrication technology.

Branched nanowires (NWs) are a novel class of composite materials with increased surface area relative to their pristine one-dimensional counterparts. Accordingly, they are good choice for gas sensing studies. In this study, p-n, TeO2-branched SnO2 NWs were produced by a two-step catalyst-assisted vapor-liquid-solid (VLS) growth technique for gas sensing studies. First, SnO2 NWs were synthesized from highly pure Sn powders, and TeO2 branches were subsequently added. The fabricated samples were well characterized in terms of morphology, crystallinity, and chemical composition. Gas sensing results exhibited the enhanced NO2 sensing capability of TeO2 branched SnO2 NW sensors relative to pristine SnO2 NWs. In particular, the maximum responses (Rg/Ra) of pristine and TeO2 branched SnO2 sensors to 10 ppm NO2 were 6.34 and 10.25, respectively. Furthermore, dynamics of TeO2 branched sensor at the optimal temperature was faster. Superior sensing properties of TeO2 branched SnO2 NWs were related to the high surface area of the branched sensors and creation of p-n heterojunctions on the surfaces of this sensor. We believe that branching is a good way to realize gas sensors for practical usages.

In view of the various qualifications required of materials nowadays, efforts to change the characteristics of inherent materials have continued. However, most material conversion techniques that have been used in the past, such as alloy design and doping effect, cannot overcome the limitation that properties are only added to the original characteristics of pristine materials. Therefore, herein, we introduced a new material design technique, a so-called “Molecular Group System”, which is completely different from existing methods. Since whole-set-systems are considered one-energetic-unit-system, either only the merits of the constituent elements can be emphasized or new materials completely different from the raw ones can be synthesized. In this study, block-stacking bottom-up approach was employed to form a one group system from SnO2, SnOx, Sn, and graphene powders, and a binder, using high-energy irradiation. Then, we discussed theoretical verifications such as SnO2-reduction and Sn-channeling.

A novel gas sensor fabricated from ZnO-shelled Si nanowires (SiNWs) is presented. After coating a thin layer of Au on the surfaces of Si NWs, ZnO layers were formed on the surfaces of p-SiNWs by thermal evaporation of Zn powders and a subsequent oxidation process. Microscopic analysis confirmed the successful formation of ZnO-Si core-shell NWs with Au nanoparticles present on the shell surface. The gas sensing performance of the gas sensor fabricated using the p-Si/n-ZnO core-shell NWs was evaluated for various gases. The sensor exhibited outstanding response and selectivity to H2S gas. The gas sensing mechanism was evaluated in detail and attributed to various factors, including the formation of ZnO/Si and Au/ZnO heterojunctions and the chemical attraction between ZnO and Au. The results demonstrate a new sensing material for H2S detection in various fields that can be easily incorporated into Si-based devices.

Branched nanowires (b-NWs) have been used for advanced applications because of their nanoscale dimensions, high surface area, and scalable synthetic methods. Herein, for the first time, we report the fabrication of Au-functionalized ZnO-branched SnO2 NWs for enhanced gas sensing application. As-fabricated NWs were structurally and morphologically investigated by X-ray diffraction, scanning electron microscopy as well as transmission electron microscopy to reveals the crystallinity and morphology of NWs. By comparing the gas sensing properties of Au-functionalized b-NWs, b-NWs, and pristine SnO2 NWs gas sensors, in terms of their sensitivity and cross-sensitivity towards NO2, we demonstrate the superior sensing properties of Au-functionalized b-NWs sensors. In particular the Au-functionalized b-NWs sensor showed a response (Rg/Ra) of 13.07 to 10 ppm NO2 gas which was higher than those of b-NWs, and pristine SnO2 NWs gas sensors. In addition to the special architecture of sensors (i.e. ZnO b-NWs on SnO2 NWs), which produces a large number of hetero- and homojunctions (a branching effect), Au acts as a catalyst to further improve the sensing characteristics of this particular sensor (a functionalization effect). According to the obtained results, we believe that metal oxide gas sensors based on noble metal-functionalized b-NWs, which use a facile synthesis procedure and produce enhanced sensing performance, will play a vital role in the future of the sensor industry.

We report the electrical and optical characteristics of SnO2 thin films irradiated by microwaves (MWs) and grown using atomic layer deposition in a commercial MW oven operating at a frequency of 2.45 GHz. The properties of the MW-irradiated SnO2 thin films were compared with those of the as-deposited SnO2 thin films. After MW irradiation, the conductivity and transparency of the thin films were enhanced. In addition, the samples irradiated for 5 min showed optimal carrier concentration, Hall mobility, resistivity, and transmittance values of 1.5 × 1020 cm−3, 4.6 cm2/V s, 8 × 10−3 Ω cm, and 95.77%, respectively. The improved properties of the MW-irradiated samples were attributed mainly to the formation of an oxygen vacancy in the SnO2 lattice during MW irradiation. Our results can be applied for the fabrication of pure SnO2-based transparent conductive oxides; these oxides are generally doped with other elements.

An unstable energy-unbalanced state such as superheating or supercooling is often unexpectedly observed because a factor of energy depends not only on the temperature but is a product of temperature (T) and entropy (S). Thus, at the same temperature, if the entropy is different, the total energy of the system can be different. In such cases, the temperature-change-rate cannot match the entropy-change-rate, which results in a hysteresis curve for the temperature/entropy relationship. Due to the difference between the temperature- and entropy-change-rates, properties of a material, such as the boiling and freezing points, can be extended from point to area. This study confirmed that depending on the heating rate, tin powders exhibit different melting points. Given the contemporary reinterpretation of many energy-non-equilibrium phenomena that have only been discussed on the basis of temperature, this study is expected to contribute to the actual expansion of scientific/engineering applications.

Breakthrough process technologies have been introduced that can increase the chemical sensitivity of an interface at which reactions occur without significantly altering the physico-chemical properties of the material. Such an interfacial treatment method is based on amorphous-carbon as a base so that fluids can be deposited, and the desired thickness and quality of the deposition can be ensured irrespective of the interface state of the material. In addition, side effects such as diffusion and decreasing strength at the interface can be avoided. This is simpler than existing vacuum-based deposition technology and it has an unmatched industrial advantage in terms of economics, speed, accuracy, reliability, accessibility, and convenience. In particular, this amorphous-carbon interface treatment technology has been demonstrated to improve gas-sensing characteristics of NO2 at room temperature.

We report the gas-sensing properties of pristine and SnS2 functionalized TeO2 nanowires (NWs). TeO2 NWs were synthesized by a vapor–liquid–solid growth method, and SnS2 functionalization was performed using an atomic layer deposition technique followed by thermal treatment. Structural and morphological analyses verified the formation of pristine and SnS2 functionalized TeO2 NWs with desired composition, phase, and morphology. Interestingly, sensing results showed that the pristine TeO2 NW gas sensor had better sensing properties relative to the SnS2 functionalized TeO2 NW gas sensor. An underlying sensing mechanism is explained in detail, and reasons for the decrease of sensing performance with the SnS2 functionalized TeO2 NW sensor was attributed to the coverage of TeO2 surface by the SnS2 nanoparticles.

We present a highly sensitive and selective NO2 sensor based on Bi2O3 branched SnO2 nanowires (NWs). SnO2 NWs were first synthesized by a vapor-liquid-solid method, were coated with an Au layer, and Bi2O3 branches were grown on their stems by the same procedure used for pure Bi powders. The fabricated sensor showed a high response (Rg/Ra) of 56.92 to 2 ppm of NO2 gas at an optimal temperature. Furthermore, its response to other interfering gases such as ethanol, acetone, toluene, and benzene, was less than 1.55, which demonstrated excellent selectivity of the sensor towards NO2 gas. For comparison and to better understand the sensing mechanism, a pristine SnO2 NWs sensor was also tested. The superior sensing properties of the branched NW sensor relative to the pristine sensor were mainly attributed to the high surface area of the sensor resulting from Bi2O3 branching, as well as the formation of homo-and heterojunctions (Bi2O3-SnO2). In addition, several factors including the presence of Au contributed to the excellent selectivity to NO2 gas. Based on the results obtained in this work, we believe that the present sensor with an easy fabrication method, along with its high sensitivity and selectivity towards NO2, can be used for the detection of NO2 gas in real applications.

We present a dual sensitization gas sensor for selective detection of either H2S or C2H5OH gases, based on ZnO/CuO nanoparticle (NP)-decorated MWCNTs. First, Cu-Zn layers of three different thickness (3, 6, 9 nm) were successfully deposited on the surfaces of CNTs by a sputtering process and subsequently converted to their corresponding oxides by thermal annealing. The gas sensing characteristics of metal oxide decorated-MWCNTs were studied in the presence of three gases, namely NO2, H2S, and C2H5OH. The best sensing properties were obtained when the Cu-Zn deposition layer was 6 nm thick. The optimized sensor showed extraordinary responses to both H2S and C2H5OH gases at working temperatures of 100 °C and 200 °C, respectively. Therefore, selectivity was tuned by selection of the working temperature. The sensing mechanisms of the metal oxide-decorated CNTs sensors are discussed in detail. The approach described, namely co-decoration of the surfaces of MWCNTs with different metal oxides, will be of great utility to researchers who wish to fabricate dual sensitive gas sensors.

Pristine and Al-doped SnO2 nanoparticles with different amounts of Al dopant were synthesized using a conventional hydrothermal process. The existing SnO2 exhibited simple interstitial physical bonding (SnO2–Al (1:0.16)) with the Al dopant; however, with an increase in the Al concentration, the bonding changed to substitutional chemical bonding (SnO2–Al (1:0.33)). We found that this crystal structural change is strongly interrelated with surface reactivity; the optimized Al-doped SnO2 nanoparticles-based sensor exhibited a significantly improved response of 17.38 – 20 ppm H2S gas with a response time of 35 s. The enhanced gas response was related to the high surface area of the optimal gas sensor (BET surface area = 78.087 m3/g) as well as the beneficial effects of Al doping. It is highlighted that this simple technique of engineering the bonding characteristics can be widely applied to other semiconducting metal oxides.

In this study, a peculiar configuration for a gas sensor consisting of vertically aligned silicon nanowires (VA-Si NWs) synthesized by metal-assisted chemical etching (MACE) is reported. Si NWs were prepared via a facile MACE method and subsequent thermal annealing. Etching was performed by generation of silver nanoparticles (Ag NPs) and subsequent etching in HF/H2O2 aqueous solution; the growth conditions were optimized by changing the process parameters. Highly vertically oriented arrays of Si NWs with a straight-line morphology were obtained, and a top–top electrode configuration was applied. The VA-Si NW gas sensor showed good sensing performance, and the VA-Si NWs exhibited a remarkable response (Rg/Ra = 11.5 ∼ 17.1) to H2 gas (10–50 ppm) at 100 °C which was the optimal working temperature. The formation mechanism and gas sensing mechanism of VA-Si NWs are described. The obtained results can suggest new approaches to making inexpensive, versatile, and portable sensors based on Si NWs having a novel top–top electrode structure that are fully compatible with well-developed Si technologies.

In this study, multi-walled carbon nanotubes (MWCNTs) were decorated by the Cu2O/CuO nanoparticles for gas sensing. For this purpose, Cu layer with different thicknesses of 3, 6, and 9 nm was coated on multi-walled carbon nanotubes using sputtering technique for different times of 1, 2, and 3 min at 25°C, respectively, followed by annealing at 500°C to produce isolated Cu2O/CuO islands. The synthesized products were fully characterized and their expected morphology, chemical composition and phases were confirmed. The gas sensors were fabricated and the optimal sensing temperatures for H2S sensing was found to be relatively low (150 °C). With control of the size of the Cu2O/CuO nanoparticles, very high sensor response ((Rg – Ra)/Ra x 100) of about 1244 % to 1 ppm H2S gas was obtained, with response time and recovery time of 219 and 77 s, respectively. Since sensor response, response time, and recovery time became significantly higher, shorter, and shorter, respectively, by the Cu2O/CuO functionalization, the associated mechanisms were explained in regard to the selective sensitivity to H2S gas. In fact, Cu2O/CuO decorations not only increased the effective surface area for sensing studies, but also they acted as effective catalyst for H2S gas. By considering the energy bands, among the multi-walled carbon nanotubes-comprising interfaces, the multi-walled carbon nanotubes/CuS heterointerfaces were effective in the enhancing the sensing behavior.

The typical methods used to improve the sensing properties of metal oxide nanowire-based gas sensors include decoration of a metal catalyst on the surface of nanowires or generation of surface defects. In this study, we suggest a process for preparing a Pd metal catalyst surrounded in SnO2-x with a large number of structural defects on the surface of SnO2 nanowires for gas sensing applications. Initially, SnO2 nanowires were prepared using a simple vapor-liquid-solid method and Pd-embedded SnO2-x-decoration was achieved by flame chemical vapor deposition. Gas sensing studies demonstrated the promising effects of Pd-embedded SnO2-x-decoration. The underlying sensing mechanism was studied in detail and explained in terms of generation of oxygen defects, catalytic activity of Pd, and formation of heterojunctions in the sensing material. The results of the present study clearly demonstrate the usefulness of this simple and fast approach to significantly enhance the gas sensing properties of metal oxide nanowires.

Complex metal oxides such as functionalized branched nanowires (NWs) are a new category of nanocomposites with unique properties for gas sensing applications. In the present work, we studied the gas sensing properties of Cr 2 O 3 -functionalized ZnO-branched SnO 2 NWs, inspired by their high surface area and numerous resistive points. These NWs were studied and compared with pristine SnO 2 NWs and ZnO-branched SnO 2 NWs. To prepare the functionalized NWs, ZnO-branched SnO 2 NWs were sputter-coated with a Cr layer and then annealed at 500 °C to produce isolated Cr 2 O 3 NPs on the ZnO branches. Results of X-ray diffraction, scanning electron microscopy, and lattice-resolved transmission electron microscopy collectively showed that Cr 2 O 3 -functionalized ZnO-branched SnO 2 NWs were successfully formed. Cr 2 O 3 functionalization was found to greatly improve the sensors’ response to NO 2 gas. Furthermore, the sensors’ good selectivity was demonstrated by testing them in the presence of various interfering gases. The underlying gas sensing mechanisms are discussed herein in detail. We believe that the Cr 2 O 3 -functionalized ZnO-branched SnO 2 NWs reported herein are promising sensors for the highly sensitive and selective detection of NO 2 gas.

Microwave (MW) irradiation has obtained extensive importance in the field of synthesis and treatment of nanoparticles, because of its faster, cleaner and cost effectiveness than the other conventional and wet chemical methods. In this study, ZnO/graphene nanocomposites were prepared and subsequently post-treated by MW irradiation. Responses of the MW irradiated ZnO/graphene nanocomposites sensors were tested towards various gases including NO2, ethanol, acetone, toluene and CO and the results were compared with those of pristine ZnO and ZnO/graphene sensors without MW irradiation. It was demonstrated that the MW irradiated sensor had much higher response particularly to NO2 gas along with superior selectivity and shorter response/recovery times in comparison to unirradiated ZnO/graphene and pristine ZnO sensors. The possible underlying mechanism of this behavior is discussed in detail, mainly in terms of the MW-induced surface defects and the generation of finer ZnO nanoparticles. The results obtained demonstrated the beneficial effect of MW irradiation for enhancing the NO2-gas sensing behavior of ZnO/graphene nanocomposites, opening a new door not only to a novel synthesis of semiconductors/graphene nanocomposites, but also to a cost-effective way of improving their sensing capabilities.

We obtained extremely high and selective sensitivity to NO2 gas by fabricating graphene–SnO2 nanocomposites using a commercial microwave oven. Structural characterization revealed that the products corresponded to agglomerated structures of graphene and SnO2 particles, with small secondary SnOx (x ≤ 2) nanoparticles deposited on the surfaces. The overall oxygen atomic ratio was decreased with the appearance of an SnOx (x < 2) phase. By the microwave treatment of graphene–SnO2 nanocomposites, with the graphene promoting efficient transport of the microwave energy, evaporation and redeposition of SnOx nanoparticles were facilitated. The graphene–SnO2 nanocomposites exhibited a high sensor response of 24.7 for 1 ppm of NO2 gas, at an optimized temperature of 150 °C. The graphene–SnO2 nanocomposites were selectively sensitive to NO2 gas, in comparison with SO2, NH3, and ethanol gases. We suggest that the generation of SnOx nanoparticles and the SnOx phase in the matrix results in the formation of SnO2/SnO2 ho...

In this work, ZnO-decorated multi-walled carbon nanotube (MWCNT) nanocomposites prepared using an in-situ method involving the thermal evaporation of Zn powders in the presence of MWCNTs. The gas sensing characteristics of the MWCNT/ZnO nanocomposites are studied, and results for the material characterizations for the synthesized nanocomposites confirm the formation of well-distributed ZnO nanoparticles onto MWCNTs, creating MWCNT/ZnO nanocomposites. The gas sensing properties of the MWCNT/ZnO nanocomposite gas sensor, such as response, cross-sensitivity, and response-recovery time, are investigated and compared with a bare MWCNT sensor. The decoration of ZnO nanoparticles greatly improves the gas sensing properties of bare MWCNTs. We discussed the possible mechanisms for the enhancement of sensing capabilities. The results suggest that decoration of n-type semiconducting oxide materials, such as ZnO in the form of nanoparticles, is a promising strategy for improvement of gas sensing properties of p-MWCNTs.

We report a novel method to significantly improve the C 6 H 6 -sensing performance of Si nanowires through the combination of TeO 2 branches and Pd sensitization. The morphological investigation revealed that TeO 2 branches were densely formed on the stem nanowires (NWs). The sensor responses of the Pd-functionalized branched NWs exhibited superior sensor responses of 55.19 to C 6 H 6 gas. In particular, Pd nanoparticles enhanced the sensor response to C 6 H 6 gas most efficiently, increasing the sensor response by 173.5%. Possible mechanisms for the sensing of the Pd-decorated branched nanowires will be associated with resistance modulation along the branch TeO 2 nanowires (including catalytic Pd effects), at the networked homojunctions between the branch TeO 2 nanowires, at the boundaries of the TeO 2 nanograins, and at the Pd/TeO 2 heterojunctions.

TeO 2 nanowires with diameters ranging from a few tens to hundreds of nanometers and lengths of a few tens of micrometers were prepared by thermal evaporation of Te powder with a Co catalyst. Initially, bead-like γ-TeO 2 nanoparticles on the surface of pre-formed thick TeO 2 nanowires were heterogeneously formed. Subsequently, uniform thin TeO 2 nanowires without the γ-TeO 2 phase were homogeneously synthesized by changing only the inlet N 2 gas flow rates and keeping other process parameters constant. The morphological and microstructural evolution of the two different nanomaterials was examined by X-ray diffraction, energy-dispersive X-ray spectrometry, and scanning and transmission electron microscopy. The optical properties of the nanomaterials were also investigated using photoluminescence spectroscopy. The emission peaks in the PL measurement without the supply of N 2 gas showed a synergetic effect between (1) bead-like orthorhombic γ-TeO 2 nanoparticles that show two specific emission bands at 388 nm and 590 nm; and (2) uniform tetragonal TeO 2 nanowires that show a characteristic emission band at 440 nm. In contrast, the pure tetragonal TeO 2 nanostructures synthesized under a N 2 gas flow rate of 2 standard liters per minute flow rate revealed a red-shifted emission band at 450 nm compared to heterogeneous structures of the same composition. The origins of the growth and emission mechanisms in the different TeO 2 structures are also discussed.

We prepared nanocomposites of n-SnO2/p-Co3O4 for application in chemical sensors. In order to fabricate p-Co3O4-decorated n-SnO2 nanowires, we sputtered a Co layer and subsequently annealed the material in air ambient. Characterization revealed that crystalline cubic Co3O4 with a tubular-like structure was attached to the surface of SnO2 core nanowires. We carried out sensing tests at 573 K in at NO2 gas concentrations ranging between 2 and 10 ppm. The sensor response was increased both by adding the Co3O4 layer and also by decreasing the thickness of the Co3O4 layer from 19.2 to 6.4 nm. We proposed possible mechanisms to explain the enhanced sensor properties obtained by Co3O4-functionalization. Co3O4-functionalized SnO2 nanowires exhibited a higher sensor response than pristine nanowires, not only due to the heterostructure-induced depletion of n-SnO2 region but also due to the surface effects of Co3O4. The generation of hole-accumulated Co3O4 layer in case of thicker-layered nanowires will decrease the sensor response. We demonstrated that Co3O4-functionalized SnO2 nanowire sensors can be used as gas sensors at very low concentrations.

Theoretical advances in science are inherently time-consuming to realise in engineering, since their practical application is hindered by the inability to follow the theoretical essence. Herein, we propose a new method to freely control the time, cost, and process variables in the fabrication of a hybrid featuring Au nanoparticles on a pre-formed SnO2 nanostructure. The above advantages, which were divided into six categories, are proven to be superior to those achieved elsewhere, and the obtained results are found to be applicable to the synthesis and functionalisation of other nanostructures. Furthermore, the reduction of the time-gap between science and engineering is expected to promote the practical applications of numerous scientific theories.

Herein, we present the effect of electron-beam irradiation (EBI) on the gas-sensing properties of Pd-functionalized reduced graphene oxide (RGO). Scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy were used to characterize the synthesized products. The samples were irradiated using electron beams at doses of 0 (Pd-RGO-0), 100 (Pd-RGO-100), and 500 kGy (Pd-RGO-500), and the NO2 gas-sensing properties were investigated. It was found that irradiation by electron beams has a critical effect on the gas-sensing properties of the samples, and the Pd-RGO-500 sensor showed the highest response to NO2 gas. In particular, the response of the unirradiated sensor and the sensor irradiated at doses of 100 and 500 kGy to 10 ppm NO2 were 1.027, 1.045, and 1.047, respectively. The response times of Pd-RGO-0, Pd-RGO-100, and Pd-RGO-500 to 10 ppm NO2 gas were 389, 335, and 345 s, respectively. The corresponding recovery times for these sensors were 808, 766, and 816 s, respectively. The increased numbers of oxygen functional groups and high-energy defects were the main reasons for the increased gas response. This study will eventually lead to increased performance levels of RGO-based sensors that use EBI, as this technology can introduce changes into materials in a non-contact, clean, and powerful manner.

We explored NO2 sensing performance of bare and SnS nanoparticle (NP)-functionalized SnO2 nanowires (NWs). The SnO2 NWs were synthesized and functionalization with SnS NPs was done by atomic layer deposition with subsequent annealing. The NO2 gas sensing results revealed that at temperatures up to 100 °C, the performance of the SnS-coated SnO2 NWs was better than bare SnO2 NWs. Moreover, the response time of SnS-coated SnO2 NWs to 2 ppm NO2 was 69 s at 100 °C, namely 9.1 times faster than that of bare SnO2 NWs. The sensing mechanisms related to the SnS-functionalized SnO2 gas sensor were proposed. The obtained results could present possibilities for the realization of low-temperature SnO2 NW-based gas sensors.

Nanodiamond (ND) was successfully synthesized using single-walled carbon nanotubes (SWCNTs) as a pure solid carbon source by means of a spark plasma sintering process. Raman spectra and X-ray diffraction patterns revealed the generation of the cubic diamond phase by means of the SPS process. Lattice-resolved TEM images confirmed that diamond nanoparticles with a diameter of about ∼10 nm existed in the products. The NDs were generated mainly through the gas-phase nucleation of carbon atoms evaporated from the SWCNTs.

The purpose of this work is to develop an eddy current testing method to predict the general corrosion behavior of Alloy 690 steam generator tubes. A corrosion test was conducted for tubes with different levels of eddy current noise in simulated primary water at 330 °C, and their corrosion behavior was correlated with the tube noise measured using bobbin and rotating probes. The corrosion behavior was closely correlated with the tube noise measured using a rotating probe. However, there was no correlation between the corrosion behavior and the tube noise measured using a bobbin probe. The tube noise value measured using a rotating pancake coil probe is suggested to be a significant parameter in estimating the general corrosion behavior of tubes.

We fabricated gas sensors by decorating amorphous carbon layers on the surfaces of SnO2 nanowires. Pretreatment and functionalization were not required for the synthesis of the SnO2-based nanocomposite, requiring only short few-second processing times. A sensing mechanism is proposed to explain the room-temperature (24 °C) operation of the gas sensor. The amorphous carbon not only increased the surface area, but also provided electronic effects improving the NO2 gas sensing likely by supplying electrons to the SnO2 and/or changing the conducting channel width inside the SnO2 by carrier transfer. The optimized gas sensor, having high response and high selectivity, can be utilized for room-temperature NO2 gas sensing applications.

Until now, the synthesis of cationic vanadate nanofibers/conducting polymers composites have required template such as surfactants and electrochemical equipment for the coating of conducting polymers. The cationic vanadate nanofibers have been synthesized by complex methods to overcome the low electrical conductivity of bulk vanadium oxide (V2O5). However, in some cases a reaction time of at least 10 h is needed. In this study, for the first time, Poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS) intercalated ammonium vanadate ((NH4)2V6O16∙1.5H2O) nanofiber (AVNF) composites were synthesized in 4 h using a simple sonochemical method for NH3 gas sensing studies. In addition, chemical composition, crystal morphologies and structures changes of the nanofiber composites according to the intercalation of ammonium cation and PSS:PEDOT were investigated. The NH3 gas sensing results reveal that the fabricated PEDOT:PSS-AVNF composite sensor had higher sensitivity and shorter response time to NH3 gas than V2O5, PEDOT, AVNF, and PEDOT-AVNF sensors at room temperature (24 °C). The enhanced NH3 sensitivity was mainly attributed to enhanced electrical conductivity (4.5 × 10−2 S. cm-1), high surface area, and p-p heterojunctions formed between the PEDOT:PSS and AVNF. The results obtained in this research demonstrate the beneficial effects of intercalating PEDOT:PSS in AVNF for NH3 gas sensing.

We present novel research devoted to the synthesis of SnO2-ZrO2 core-shell nanowires (C-S NWs) and investigation of their NO2 gas sensing properties. ZrO2 shell layer was deposited on networked SnO2 NWs. The ZrO2 shell thickness was varied using four different numbers of atomic layer deposition (ALD) cycles (50, 100, 150 and 200). Structural, morphological and chemical composition of the synthesized products were confirmed by different characterization techniques. The gas sensors showed an optimal sensing temperature at a relatively low temperature (≤ 150 °C). NO2 sensing results showed a strong dependence of response on the thickness of the ZrO2 shell, or equivalently the number of ALD cycles of ZrO2. The optimal sensor with a ZrO2 shell deposited at 150 ALD cycles (24.1 nm thick) exhibited a high response of (Rg/Ra) 24.7–10 ppm NO2 gas and revealed a good selectivity to NO2 gas. Also, with an increase in the thickness of the ZrO2 shell, the negative influence of humidity on the sensor response to NO2 was significantly decreased. The sensing mechanism involves NO2 removing electrons from the ZrO2 shell. The dependence of responses to shell thickness was explained based on two different regimes, i.e., the surface-electron-limiting regime and adsorbing species-limiting regime. The results obtained in this study can be used for further exploration of the sensing properties of ZrO2 as a novel shell material.

After the Cu coating layer was fabricated, the high energy beam was irradiated and the mechanical properties of the Cu coating layer before and after irradiation were compared. As the high energy beam is irradiated onto the material of the coating layer, the dipole of the polar material rotates, and the coating layer is heated due to the intermolecular friction, thereby resulting in a heat treatment effect even in a short time. Scanning electron microscopy analysis confirmed that the surface structure was changed, and X-ray diffraction and X-ray photoelectron spectroscopy were used to confirm the crystallinity and bonding state from Cu to CuO. In addition, in the nanoindentation analysis, all improved mechanical properties were observed for martens hardness, indentation hardness and indentation modulus. It is clear that this method will be widely used in various fields in the near future to change the surface layer phase to improve mechanical properties.

Sub-20-nm Ag nanoparticles created via sputtering were freely moved into preformed Si pores and were arranged along both wall and lower surfaces in etched Si layers via a post-thermal annealing treatment. The variously sized Ag quantum dots on the porous Si facilitate broadband visible emission via photo-generated enhanced luminescent effects, i.e., plasmonic effects of Ag nanoparticles by electron transfer from the Si-based matrix to the metallic Ag. The emission wavelengths and intensities, depending on the sizes of the Ag quantum dots, were determined by the degree of oxidation of the Si-based substrate such as Si, SiOx, and SiO2, according to different post-thermal annealing conditions. The morphological, microstructural, and optical evolution of Ag nanoparticles and Si pores were simply observed via side-cross-sectional scanning electron microscopy, X-ray diffraction, transmission electron microscopy, and crystalline-controlled photoluminescence analyses, respectively. The origin of a new systematic luminescence mechanism based on energy-equilibria is also presented.

With high-performance room-temperature gas sensors being in great demand from an energy-saving standpoint, in this study, we fabricated porous silicon (PS) sensors by electrochemically etching at different times (30, 60, and 90 min). The porous nature of the etched PSs was studied using scanning electron microscopy, and subsequently gas sensors were fabricated. NO2 sensing studies showed that the highest gas performance can be obtained at room temperature (30 °C). Furthermore, the PS sensor etched for 60 min had the best performance among the sensors, which is related to its higher surface area and high enough initial resistance. In particular for the PS sensor etched for 60 min, the response (Ra/Rg) to 10 ppm NO2 was 9.56, which was much higher than other interfering gases, demonstrating its high selectivity towards NO2 gas. This study reveals the need for optimization of electrochemical etching to realize gas sensors based on PS working at room temperature.

We report the room-temperature sensing characteristics of Si nanowires (NWs) fabricated from p-Si wafers by a metal-assisted chemical etching method, which is a facile and low-cost method. X-ray diffraction was used to the the study crystallinity and phase formation of Si NWs, and product morphology was examined using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). After confirmation of Si NW formation via the SEM and TEM micrographs, sensing tests were carried out at room temperature, and it was found that the Si NW sensor prepared from Si wafers with a resistivity of 0.001–0.003 Ω.cm had the highest response to NO2 gas (Rg/Ra = 1.86 for 50 ppm NO2), with a fast response (15 s) and recovery (30 s) time. Furthermore, the sensor responses to SO2, toluene, benzene, H2, and ethanol were nearly negligible, demonstrating the excellent selectivity to NO2 gas. The gas-sensing mechanism is discussed in detail. The present sensor can operate at room temperature, and is compatible with the microelectronic fabrication process, demonstrating its promise for next-generation Si-based electronics fused with functional chemical sensors.

Dissolving microneedles (DMNs) have been widely studied in medical applications due to their pain-free administration, superior efficiency, and safe drug delivery. In skin vaccination, preserving the activity of the encapsulated antigen is an important consideration, as antigen activity is lost during DMN fabrication because of various stress factors. These stress factors vary between fabrication methods and each method affects the antigen's activity to different degrees. In this study, the activity of encapsulated antigens delivered by DMNs is compared between two recently developed DMN fabrication methods; droplet-born air blowing (DAB) and centrifugal lithography (CL) for a model scrub typhus vaccine antigen, ScaA. Although the in vitro analysis of ScaA-loaded DMNs (ScaA-DMNs) does not show any differences in physical properties depending on the fabrication methods, the immunogenicity of the CL-produced ScaA-DMN is significantly higher based on cytokine measurement and humoral immunity. DAB and CL differ in their solidification conditions, suggesting that solidification factors critically affect the encapsulated antigen's activity. ScaA-DMNs may also be stably stored for 4 weeks at room temperature. In conclusion, CL is a superior DMN fabrication method compared with DAB, and this study proves that DMN is feasible and practical for skin vaccination.