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Here, we report on using chemical vapor deposition to generate three kinds of gallium sulfide nanosheets, with thicknesses of approximately 10, 40, and 170 nm. Next, we performed Raman imaging analysis on these nanosheets to evaluate their properties. The 10 nm GaS nanosheets exhibited a nearly equal distribution of Raman imaging intensity, whereas the 40 and 170 nm GaS nanosheets exhibited an inclination toward the edges with higher Raman intensity. When the polarization of the laser was changed, the intensity of Raman imaging of the 10 nm thick GaS nanosheets remained consistent when illuminated with a 532 nm laser. Notably, a greater Raman intensity was discernible at the edges of the 40 and 170 nm GaS nanosheets. Three distinct GaS nanosheet devices with different film thicknesses were fabricated, and their photocurrents were recorded. The devices were exposed to light of 455 nm wavelength. The GaS nanosheet devices with film thicknesses of 40 and 170 nm exhibited a positive photoresponse even though the photocurrents were fairly low. In contrast, the GaS nanosheet device with a film thickness of 10 nm had a considerable current without light, even though it had a weak reaction to light. This study reveals the different spatial patterns of Raman imaging with GaS thickness, the wavelength of excitation light, and polarization. Remarkably, the I-V diagram revealed a higher dark-field current of 800 nA in the device with a GaS nanosheet thickness of approximately 10 nm, when using a voltage of 1.5 V and a laser of 445 nm wavelength. These findings are comparable with those theretical pretictions in the existing literature. In conclusion, the observation above could serve as a catalyst for future exploration into photocatalysis, electrochemical hydrogen production through water splitting, energy storage, nonlinear optics, gas sensing, and ultraviolet selective photodetectors of GaS nanosheet-based photodetectors.

We have designed a new ternary structure to enhance the sensing properties of WS2 nanosheet (NS)-based gas sensors at room temperature (RT) in self-heating mode. SnO2 nanowires (NWs, 10–30 wt%) were added to WS2 NSs and then Au nanoparticles (NPs) were deposited on the surface of the resulting composites by UV irradiation. The Au-decorated 10 wt% SnO2–WS2 composition showed the highest gas sensing properties. The presence of SnO2 NWs on the WS2 NSs effectively enhanced the diffusion and adsorption of gas species into deeper parts of the gas sensor. Furthermore, the chemical sensitization of Au (increase in oxygen ionosorption; spillover effect and catalytic effect towards CO) contributed to an enhanced response to CO gas. Gas sensing tests performed in the self-heating mode demonstrated the possibility of realizing a low-voltage, low-power-consumption CO gas sensor based on the Au-decorated 10 wt% SnO2–WS2. The sensor response under 60% relative humidity (RH) conditions was 84% of that under dry conditions, which shows that CO sensing is possible in wet environments at room temperature operation.

Pure SnO2 and 1 at.% PdO–SnO2 materials were prepared using a simple hydrothermal method. The micromorphology and element valence state of the material were characterized using XRD, SEM, TEM, and XPS methods. The SEM results showed that the prepared material had a two-dimensional nanosheet morphology, and the formation of PdO and SnO2 heterostructures was validated through TEM. Due to the influence of the heterojunction, in the XPS test, the energy spectrum peaks of Sn and O in PdO–SnO2 were shifted by 0.2 eV compared with SnO2. The PdO–SnO2 sensor showed improved ethanol sensing performance compared to the pure SnO2 sensor, since it benefited from the large specific surface area of the nanosheet structure, the modulation effect of the PdO–SnO2 heterojunction on resistance, and the catalyst effect of PdO on the adsorption of oxygen. A DFT calculation study of the ethanol adsorption characteristics of the PdO–SnO2 surface was conducted to provide a detailed explanation of the gas-sensing mechanism. PdO was found to improve the reducibility of ethanol, enhance the adsorption of ethanol’s methyl group, and increase the number of adsorption sites. A synergistic effect based on the continuous adsorption sites was also deduced.

Shaping crystalline porous materials such as metal organic frameworks (MOFs) and zeolites into two-dimensional (2D) nanosheet forms is highly desirable for developing high-performance molecular sieving membranes. However, conventional exfoliation–deposition is complex and challenging for the large-scale fabrication of nanosheet MOF tubular membranes. Here, for the first time, we report a direct growth technique by ZnO self-conversion and ammonia assistance to fabricate zeolitic imidazolate framework (ZIF) membranes consisting of 2D nanosheets on porous hollow fiber substrates; the membranes are suitable for large-scale industrial gas separation processes. The proposed fabrication process for ZIF nanosheet membranes is based on the localized self-conversion of a pre-deposited thin layer of ZnO in a ligand solution containing ammonium hydroxide as a modulator. The resulting ZIF 2D nanosheet tubular membrane is highly oriented and only 50 nm in thickness. It exhibits excellent molecular sieving performance, with high H 2 permeance and selectivity for H 2 /CO 2 separation. This technique shows great promise in MOF nanosheet membrane fabrication for large-scale molecular sieving applications.

The unique properties of MoS2 nanosheets make them a promising candidate for high-performance room temperature gas detection. Herein, few-layer MoS2 nanosheets (FLMN) prepared via mechanical exfoliation are coated on a substrate with interdigital electrodes for room-temperature NO2 detection. Interestingly, compared with other NO2 gas sensors based on MoS2, FLMN gas sensors exhibit high responsivity for room-temperature NO2 detection, and NO2 is easily desorbed from the sensor surface with an ultrafast recovery behavior, with recovery times around 2 s. The high responsivity is related to the fact that the adsorbed NO2 can affect the electron states within the entire material, which is attributed to the very small thickness of the MoS2 nanosheets. First-principles calculations were carried out based on the density functional theory (DFT) to verify that the ultrafast recovery behavior arises from the weak van der Waals binding between NO2 and the MoS2 surface. Our work suggests that FLMN prepared via mechanical exfoliation have a great potential for fabricating high-performance NO2 gas sensors.

Polyaniline (PANI) is an important conductive-polymer gas-sensing material with working temperature and mechanical flexibilities superior to those of conventional metal oxide sensing materials. However, its applicability is limited by its low sensitivity, high detection limits, and long response/recovery times. In this study, we prepared PANI/WS2 composites via chemical oxidative polymerization and mechanical blending. A multilayer sensor structure—sequentially printed silver-paste heating electrodes, fluorene polyester insulating layer, silver interdigitated electrodes, and sensing material layer—was fabricated on a polyimide substrate via flexible microelectronic printing and systematically characterized using scanning electron microscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy. The optimized 5 wt% WS2 composite showed enhanced gas-sensing performance, with 219.1% sensitivity to 100 ppm ammonia (2.4-fold higher than that of pure PANI) and reduced response and recovery times of 24 and 91 s, respectively (compared to 81 and 436 s for pure PANI, respectively). Notably, the PANI/WS2 sensor detected an ultralow ammonia concentration (100 ppb) with 0.104% sensitivity. The structural characterization and performance analysis results were used to deduce a mechanism for the enhanced sensing capability. These findings highlight the application potential of PANI/WS2 composites in flexible gas sensors and provide fundamental insights for PANI-based sensing materials research.

Electrochemical reduction of NO offers us an attractive alternative to traditional selective catalytic reduction process for harmful NO removal and simultaneous NH 3 production, but it requires efficient electrocatalyst to enable the NO reduction reaction with high selectivity. Here, we report on the development of Bi nanoparticles/carbon nanosheet composite (Bi@C) for highly effective NO reduction electrocatalysis toward selective NH 3 formation. Such Bi@C catalyst attains an impressive NH 3 yield of 1,592.5 µg·hr −1 ·mg cat. −1 and a high Faradaic efficiency as high as 93% in 0.1 M Na 2 SO 4 electrolyte. Additionally, it can be applied as efficient cathode materials for Zn−NO battery to reduce NO to NH 3 with high electricity generation.

The development of low-cost and low-power gas sensors for reliable NO2 gas detection is important due to the highly toxic nature of NO2 gas. Herein, initially, SnO2 nanowires (NWs) were synthesized through a simple vapor–liquid–solid growth mechanism. Subsequently, different amounts of SnO2 NWs were composited with MoS2 nanosheets (NSs) to fabricate SnO2 NWs/MoS2 NS nanocomposite gas sensors for NO2 gas sensing. The operation of the sensors in self-heating mode at 1–3.5 V showed that the sensor with 20 wt.% SnO2 (SM-20 nanocomposite) had the highest response of 13 to 1000 ppb NO2 under 3.2 V applied voltage. Furthermore, the SM-20 nanocomposite gas sensor exhibited high selectivity and excellent long-term stability. The enhanced NO2 gas response was ascribed to the formation of n-n heterojunctions between SnO2 NWs and MoS2, high surface area, and the presence of some voids in the SM-20 composite gas sensor due to having different morphologies of SnO2 NWs and MoS2 NSs. It is believed that the present strategy combining MoS2 and SnO2 with different morphologies and different sensing properties is a good approach to realize high-performance NO2 gas sensors with merits such as simple synthesis and fabrication procedures, low cost, and low power consumption, which are currently in demand in the gas sensor market.

In this paper, mesoporous ZnO nanosheets were synthesized by the hydrothermal method using polystyrene-polyacrylic acid (PS-PAA) as the template. The morphology, structure, and composition of the samples were characterized by SEM, TEM, XRD, and XPS, and the physical properties of the samples were tested by N2 adsorption–desorption curve. The results showed that the mesoporous ZnO nanosheets presented a flower-like appearance. Each flower is composed of flake petals which consist of nanoparticles of different sizes, with a large specific surface area. Gas sensitivity test results show that the ZnO gas sensor has good triethylamine (TEA) sensing performance. Its response to 50 ppm TEA can reach 43.771, and the detection limit is as low as 1 ppm, showing the characteristics of rapid response/recovery.

Gas‐mediated sonodynamic therapy (SDT) has the potential to become an effective strategy to improve the therapeutic outcome and survival rate of cancer patients. Herein, titanium sulfide nanosheets (TiSX NSs) are prepared as cascade bioreactors for sequential gas–sonodynamic cancer therapy. TiSX NSs themselves as hydrogen sulfide (H2S) donors can burst release H2S gas. Following H2S generation, TiSX NSs are gradually degraded to become S‐defective and partly oxidized into TiOX on their surface, which endows TiSX NSs with high sonodynamic properties under ultrasound (US) irradiation. In vitro and in vivo experiments show the excellent therapeutic effects of TiSX NSs. In detail, large amounts of H2S gas and reactive oxygen species (ROS) can simultaneously inhibit mitochondrial respiration and ATP synthesis, leading to cancer cell apoptosis. Of note, H2S gas also plays important roles in modulating and activating the immune system to effectively inhibit pulmonary metastasis. Finally, the metabolizable TiSX NSs are excreted out of the body without inducing any significant long‐term toxicity. Collectively, this work establishes a cascade bioreactor of TiSX NSs with satisfactory H2S release ability and excellent ROS generation properties under US irradiation for programmed gas–sonodynamic cancer therapy. Titanium sulfide (TiSX) nanosheets synthesized via a convenient high‐temperature organic‐phase method are used as a cascade bioreactor for H2S‐mediated programmed gas–sonodynamic cancer therapy.