scholarly journals Ultrafast Growth of h-MoO3 Microrods and Its Acetone Sensing Performance

Surfaces ◽  
2020 ◽  
Vol 4 (1) ◽  
pp. 9-16
Author(s):  
Giovana T. Santos ◽  
Anderson A. Felix ◽  
Marcelo O. Orlandi

Hexagonal molybdenum trioxide (h-MoO3) was synthesized by microwave-assisted hydrothermal method, allowing an ultrafast growth of unidimensional microrods with well-faceted morphology. The crystalline structure of this metastable phase was confirmed by X-ray diffraction (XRD) and Raman spectroscopy. Scanning electron microscopy (SEM) showed that hexagonal microrods can be obtained in one minute with well-defined exposed facets and the fine control of morphology. Sensing tests of the acetone biomarker revealed that the h-MoO3 microrods exhibit, at low ppm level, good sensor signal, fast response/recovery times, selectivity to different interferent gases, and a lower detection limit of 400 ppb.

Sensors ◽  
2020 ◽  
Vol 20 (23) ◽  
pp. 6830
Author(s):  
Piotr Nowak ◽  
Wojciech Maziarz ◽  
Artur Rydosz ◽  
Kazimierz Kowalski ◽  
Magdalena Ziąbka ◽  
...  

Thin-film n-n nanoheterostructures of SnO2/TiO2, highly sensitive to NO2, were obtained in a two-step process: (i) magnetron sputtering, MS followed by (ii) Langmuir-Blodgett, L–B, technique. Thick (200 nm) SnO2 base layers were deposited by MS and subsequently overcoated with a thin and discontinuous TiO2 film by means of L–B. Rutile nanopowder spread over the ethanol/chloroform/water formed a suspension, which was used as a source in L–B method. The morphology, crystallographic and electronic properties of the prepared sensors were studied by scanning electron microscopy, SEM, X-ray diffraction, XRD in glancing incidence geometry, GID, X-ray photoemission spectroscopy, XPS, and uv-vis-nir spectrophotometry, respectively. It was found that amorphous SnO2 films responded to relatively low concentrations of NO2 of about 200 ppb. A change of more than two orders of magnitude in the electrical resistivity upon exposure to NO2 was further enhanced in SnO2/TiO2 n-n nanoheterostructures. The best sensor responses RNO2/R0 were obtained at the lowest operating temperatures of about 120 °C, which is typical for nanomaterials. Response (recovery) times to 400 ppb NO2 were determined as a function of the operating temperature and indicated a significant decrease from 62 (42) s at 123 °C to 12 (19) s at 385 °C A much smaller sensitivity to H2 was observed, which might be advantageous for selective detection of nitrogen oxides. The influence of humidity on the NO2 response was demonstrated to be significantly below 150 °C and systematically decreased upon increase in the operating temperature up to 400 °C.


2020 ◽  
Vol 15 (1) ◽  
pp. 41-45 ◽  
Author(s):  
Zhi-Cheng Zhong ◽  
Zhao-Jun Jing ◽  
Kui-Yuan Liu ◽  
Tong Liu

We adopted the sol–gel and hydrothermal methods to prepare the TiO2 nanomaterials doped with ZnO. We adopted X-ray diffraction, scanning electron microscopy, and the Brunauer–Emmett–Teller method to investigate the materials’ structures and morphologies. The results showed that the prepared TiO2 nanomaterials had uniform size and good dispersibility. Gas sensors were fabricated and their performances in acetylene sensing were assessed. The results show that the sensor prepared with the ZnO/TiO2 nanomaterial doped with 10 wt% ZnO gave fast response and recovery times for acetylene gas at different concentrations. When the operating temperature was 280 °C, the gas sensor detected 200 ppm acetylene gas with a response sensitivity of 9.9, a response time of 5 s, and a recovery time of 2 s.


2020 ◽  
Author(s):  
Masoumeh Mohammadi ◽  
Mohammad Almasi-Kashi ◽  
Somayeh Fardindoost ◽  
Azam Iraji zad

Abstract A grid configuration based on the aligned nickel oxide nanowire (NiO NW) for humidity sensing were fabricated through the oxidation of ferromagnetic nickel NWs prepared by a template-assisted electrodeposition process. Their structure and elemental compositions were characterized by field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), and energy-dispersive X-ray analyses (EDAX). The room-temperature humidity sensing behavior of the NiO NWs was investigated successfully based on DC and AC impedance spectroscopy (IS) method in frequencies range 10 Hz to 2 MHz. The sensors showed excellent humidity sensing characteristics such as a high response of about 66 with rather rapid response-recovery times about 9 and 2 s for 90%RH, and good stability. The equivalent circuits were simulated for impedance responses to humidity in the range of 40–90% RH. According to the results, ionic conduction via NW-NW junctions as well as NW-electrode interfaces in the grid configuration is responsible for sensing behavior.


Materials ◽  
2021 ◽  
Vol 14 (20) ◽  
pp. 5913
Author(s):  
Wang-De Lin ◽  
Shu-Yun Lin ◽  
Murthy Chavali

In the present study, we report the first attempt to prepare a conducive environment for Pt/BiVO4 nanocomposite material reusability for the promotion of sustainable development. Here, the Pt/BiVO4 nanocomposite was prepared using a hydrothermal method with various weight percentages of platinum for use in NO2 gas sensors. The surface morphologies and structure of the Pt/BiVO4 nanocomposite were characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD). The results showed that Pt added to BiVO4 with 3 wt.% Pt/BiVO4 was best at a concentration of 100 ppm NO2, with a response at 167.7, and a response/recovery time of 12/35 s, respectively. The Pt/BiVO4 nanocomposite-based gas sensor exhibits promising nitrogen dioxide gas-sensing characteristics, such as fast response, highly selective detection, and extremely short response/recovery time. Additionally, the mechanisms of gas sensing in Pt/BiVO4 nanocomposites were explored in this paper.


Author(s):  
A. Leineweber ◽  
M. Löffler ◽  
S. Martin

Abstract Cu6Sn5 intermetallic occurs in the form of differently ordered phases η, η′ and η′′. In solder joints, this intermetallic can undergo changes in composition and the state of order without or while interacting with excess Cu and excess Sn in the system, potentially giving rise to detrimental changes in the mechanical properties of the solder. In order to study such processes in fundamental detail and to get more detailed information about the metastable and stable phase equilibria, model alloys consisting of Cu3Sn + Cu6Sn5 as well as Cu6Sn5 + Sn-rich melt were heat treated. Powder x-ray diffraction and scanning electron microscopy supplemented by electron backscatter diffraction were used to investigate the structural and microstructural changes. It was shown that Sn-poor η can increase its Sn content by Cu3Sn precipitation at grain boundaries or by uptake of Sn from the Sn-rich melt. From the kinetics of the former process at 513 K and the grain size of the η phase, we obtained an interdiffusion coefficient in η of (3 ± 1) × 10−16 m2 s−1. Comparison of this value with literature data implies that this value reflects pure volume (inter)diffusion, while Cu6Sn5 growth at low temperature is typically strongly influenced by grain-boundary diffusion. These investigations also confirm that η′′ forming below a composition-dependent transus temperature gradually enriches in Sn content, confirming that Sn-poor η′′ is metastable against decomposition into Cu3Sn and more Sn-rich η or (at lower temperatures) η′. Graphic Abstract


1997 ◽  
Vol 07 (03n04) ◽  
pp. 265-275
Author(s):  
R. Q. Zhang ◽  
S. Yamamoto ◽  
Z. N. Dai ◽  
K. Narumi ◽  
A. Miyashita ◽  
...  

Natural FeTiO 3 (illuminate) and synthesized FeTiO 3, single crystals were characterized by Rutherford backscattering spectroscopy combined with channeling technique and particle-induced x-ray emission (RBS-C and PIXE). The results obtained by the ion beam analysis were supplemented by the x-ray diffraction analysis to identify the crystallographic phase. Oriented single crystals of synthesized FeTiO 3 were grown under the pressure control of CO 2 and H 2 mixture gas using a single-crystal floating zone technique. The crystal quality of synthesized FeTiO 3 single crystals could be improved by the thermal treatment but the exact pressure control is needed to avoid the precipitation of Fe 2 O 3 even during the annealing procedure. Natural FeTiO 3 contains several kinds of impurities such as Mn , Mg , Na and Si . The synthesized samples contain Al , Si and Na which are around 100 ppm level as impurities. The PBS-C results of the natural sample imply that Mn impurities occupy the Fe sublattice in FeTiO 3 or in mixed phase between ilmenite and hematite.


2019 ◽  
pp. 1694-1703
Author(s):  
Reem Saadi Khaleel ◽  
Mustafa Shakir Hashim

Rapid breakdown anodization (RBA) process was used to fabricate TiO2 sensor to measure pressure and humidity and sense gases at room temperature. This chemical process transformed Ti to its oxide (TiO2) as a powder with amorphous phase as X ray diffraction (XRD) technique confirmed.  This oxide consisted from semi spherical nanoparticles and titania nanotubes (TNTs) as Scanning electron microscope (SEM) technique showed.  TiO2 powder was deposited on Ti substrates by using electrophoretic deposition (EPD) method.   Average pressure sensitivity was 0.34 MΩ/bar and hysteresis area was 1.4 MΩ .bar. Resistance of TiO2 decreased exponentially with the increasing of relative humidity (RH%). The sensitivity% of TiO2 for RH% was greater than 70% in the range of (50-95). TiO2 was tested as a sensor for Ammonia, Ethanol and Methanol. Its sensitivity and selectivity towards Ammonia were the greatest but the shortest response and recovery times were recorded toward Methanol.


Author(s):  
A. V. Maletsky ◽  
T. E. Konstantinova ◽  
D. R. Belichko ◽  
G. K. Volkova ◽  
V. V. Burkhovetsky

The paper presents results of the study of the effect of doping with yttrium oxide on ceramics of the composition (γ + θ) Al2O3 + nY2O3 (n = 0, 1, 2, 3 wt%), sintered at 1550°C for 2 h, from powders of the specified composition annealed at temperatures of 500 , 800, 1000°С. X-ray diffraction analysis established the formation in ceramics of yttrium aluminum garnet Y3Al5O12 (YAG) and a metastable phase of the same composition with a tetragonal lattice type in powders at temperatures above 1200°C. The effect of YAG on the physical and mechanical properties was established: high properties were demonstrated by ceramics of the composition α-Al2O3 + 2wt% Y2O3, obtained from a powder annealed at 1000°C. In addition, high physical and mechanical properties were observed in ceramics of the composition α-Al2O3 + 0wt% Y2O3, obtained from a powder annealed at 800°C. The effect of the so-called “mutual protection against crystallization” was discovered, which consists in the mutual inhibition of crystallization processes in powders of the Al2O3 – Y2O3 system.


2016 ◽  
Vol 869 ◽  
pp. 1001-1006
Author(s):  
Claudia Ferreira da Silva ◽  
André Lima e Silva ◽  
Francisco Xavier Nobre ◽  
Edson Cavalcanti Silva Filho ◽  
Luiz de Sousa Santos Jr. ◽  
...  

Two-dimensional microstructures of molybdenum trioxide (MoO3) were synthesized by heptamolybdate tetrahydrate ammonium acidification, followed by calcination. A solution of the precursor compound heptamolybdate tetrahydrate ammonium acidified to pH 3,5 using glacial acetic acid followed by hydrothermal treatment for 150, 180 and 200 °C for 1, 6 and 12 hours. Then, the intermediate was calcined at 300 °C for varying time 6 and 12h to obtain MoO3. X-ray diffraction revealed that the crystals grew with crystalline structure corresponding to the orthorhombic phase of MoO3 (a-MoO3) as major phase, with a preferential growth direction along the planes (0K0). Raman spectroscopy and IR confirmed the formation of the characteristic modes of molybdenum trioxide for stage found. With Scanning Electron Microscopy (SEM) was possible to observe the formation of nanoplates.


2017 ◽  
Vol 888 ◽  
pp. 404-408 ◽  
Author(s):  
Mohd Nor Latif ◽  
Alinda Samsuri ◽  
Mohamed Wahab Mohamed Hisham ◽  
Mohd Ambar Yarmo

Metallic molybdenum was synthesized through reduction of molybdenum trioxide (MoO3) by using hydrogen as a reducing agent. The reduction behavior of MoO3 were investigated by using temperature programmed reduction (TPR). The reduced phases were characterized by X-ray diffraction spectroscopy (XRD). The XRD results indicate that the reduction of MoO3 proceed in two steps reduction (MoO3 → MoO2 → Mo) with formation of intermediate phases of Mo4O11 during first step of reduction. However, the TPR results showed only one broad peak that correspond to all reduction step that was merge into one peak. It seem that, increasing the temperature cause the rapid reduction that correlated with thermodynamic consideration data that show the formation of metallic molybdenum is become feasible by increasing the temperature.


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