RESUMO
In this study, the fabrication of an ultrahigh selective NH3gas sensor based on RGO/WO3nanocomposite has been proposed. The hydrothermal method was employed to synthesize the RGO/WO3nanocomposite. The formation of RGO/WO3nanocomposite and the elemental composition, structure and morphology of the as-synthesized materials were confirmed through an array of analytical techniques, including XRD, Raman, FT-IR, XPS and TEM. For gas sensing applications, pure RGO and RGO/WO3have effectively spin-coated onto the interdigitated electrodes (IDE's) based on fluorine doped tin oxide (FTO) respectively, and their sensitivity towards NH3was tested. Gas sensing characteristics of prepared materials were analyzed at room temperature (25 °C) under different relative humidity (RH) levels. The developed RGO/WO3sensor was subjected to different NH3concentrations, demonstrating a high sensing response of 89% towards 500 ppm NH3under 11%-97%-11% RH conditions. Notably, the sensor exhibited rapid response and recovery times with an average response time of 92 s and recovery time of 26 s when exposed to 500 ppm NH3under the specified RH conditions. To gauge the material selectivity, the prepared nanocomposite was exposed to a range of volatile organic compounds and the results showcased the sensor's remarkable selectivity and sensitivity specifically toward NH3vapor. This superior performance can be attributed to the abundant active sites and the excellent electron transport properties inherent to the RGO component. Importantly, the RGO/WO3sensor displayed high reproducibility and consistent responses, with minimal degradation (1.98% degradation) over 30 d at 11%-97%-11% RH. Furthermore, we examined the sensor's response with varying levels of relative humidity to assess its potential for real-world applications. The sensor exhibited extremely low power consumption, outperforming a commercially available metal oxide sensor while operating at ambient temperature. The robust performance of RGO/WO3coupled with low power requirements and ambient temperature operation, positions it as a promising candidate for next-generation gas sensing technologies.
RESUMO
Herein, the monoclinic phase of tungsten oxide (γ-WO3) was successfully obtained after annealing hydrothermally synthesised WO3 powder at 500 °C. As per the result obtained from the N2 adsorption-desorption isotherm, the material has been identified as mesoporous with a specific surface area of 3.71 m2 g-1 from BET (Brunauer-Emmett-Teller) analysis. Moreover, the average pore size (49.52 nm) and volume (0.050 cm3 g-1) were also determined by the BJH (Barrett-Joyner-Halenda) method. FE-SEM (field emission scanning electron microscopy) and HR-TEM (high resolution transmission electron microscopy) have confirmed the formation of nanoplates with an average diameter of approximately 274 nm. Raman spectroscopy has shown peaks at the lower wavenumber region (270 cm-1 and 326 cm-1) and the higher wavenumber region (713 cm-1 and 806 cm-1) for O-W-O bending modes and stretching modes, respectively. The combined effect of relative humidity (RH-11%-RH-95%-RH-11%) and NH3 (150 ppm, 300 ppm, 450 ppm, 600 ppm, 700 ppm, and 800 ppm) was investigated in this reported work. The synthesised γ-WO3 has shown highly responsive behaviour for humidity of 96.5% (RH-11%-95%) and NH3 sensing (under humidity) of 97.4% (RH-11%-95% with 800 ppm NH3). The response and recovery time were calculated as 15 s and 52 s, and 16 s and 54 s for humidity, and NH3 under humidity, respectively. The experimental findings demonstrated that the resistance of the sensor depends on the concentration of NH3 and humidity. Moreover, γ-WO3 has been investigated as a promising catalyst for the dye degradation of methylene blue (MB) with a degradation efficiency of 72.82% and methyl orange (MO) with a degradation efficiency of 53.84% under visible light exposure. This dye degradation occurred within 160 min in the presence of a catalyst under visible light irradiation.
