scholarly journals A Highly Sensitive Room Temperature CO2 Gas Sensor Based on SnO2-rGO Hybrid Composite

Materials ◽  
2021 ◽  
Vol 14 (3) ◽  
pp. 522
Author(s):  
Zhi Yan Lee ◽  
Huzein Fahmi bin Hawari ◽  
Gunawan Witjaksono bin Djaswadi ◽  
Kamarulzaman Kamarudin
Keyword(s):  
Electron Microscopy ◽  
Carbon Dioxide ◽  
Gas Sensor ◽  
Photoelectron Spectroscopy ◽  
Hybrid Composite ◽  
Room Temperature ◽  
Co2 Gas ◽  
X Ray ◽  
Wide Range ◽  
Co2 Gas Sensor

A tin oxide (SnO2) and reduced graphene oxide (rGO) hybrid composite gas sensor for high-performance carbon dioxide (CO2) gas detection at room temperature was studied. Since it can be used independently from a heater, it emerges as a promising candidate for reducing the complexity of device circuitry, packaging size, and fabrication cost; furthermore, it favors integration into portable devices with a low energy density battery. In this study, SnO2-rGO was prepared via an in-situ chemical reduction route. Dedicated material characterization techniques including field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), energy dispersive X-ray (EDX) spectroscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS) were conducted. The gas sensor based on the synthesized hybrid composite was successfully tested over a wide range of carbon dioxide concentrations where it exhibited excellent response magnitudes, good linearity, and low detection limit. The synergistic effect can explain the obtained hybrid gas sensor’s prominent sensing properties between SnO2 and rGO that provide excellent charge transport capability and an abundance of sensing sites.

Template-free fabrication of NiO nanobelts: promising candidate for ethanol gas sensor at room temperature

2016 ◽  
Vol 33 (2) ◽  
pp. 68-72 ◽  
Author(s):  
Zhiwei Li
Keyword(s):  
Electron Microscopy ◽  
Gas Sensor ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Hydrothermal Reaction ◽  
Ethanol Vapor ◽  
Promising Candidate ◽  
Content Type ◽  
X Ray ◽  
Template Free

Purpose The purpose of this paper is to seek a surfactant or template-free, simple and green method to fabricate NiO nanobelts and to find an effective technique to detect the ethanol vapor at room temperature. Design/methodology/approach NiO nanobelts with high aspect ratio and dispersive distribution have been synthesized by a template-free hydrothermal reaction at 160°C for 12 h. The products are studied by X-ray diffraction (XRD), energy dispersive spectroscopY, scanning electron microscopy, atomic force microscopy, high-resolution transmission electron microscopy, selective area electron diffractio and X-ray photoelectron spectroscopy. In particular, the room-temperature ethanol sensitivity of NiO nanobelts is investigated by the surface photo voltage (SPV) technique. Findings The prepared NiO nanobelts is single crystalline bunsenite structure with the length of approximately 10 μm and the diameter of approximately 30 nm. The atomic ratio of “Ni” to “O” is 0.92:1. When the concentration of ethanol vapor reaches 100 ppm, the sensitivity of NiO nanobelts is 7, which can meet the commercial demanding of ethanol gas sensor. Originality/value The NiO nanobelts can be obtained by a template-free, simple and green hydrothermal reaction at 160°C for 12 h. The NiO nanobelts-based gas sensor is a promising candidate for the application in ethanol monitoring at room temperature by SPV technique.

ROOM TEMPERATURE PHOTOLUMINESCENCE OF POLYCRYSTALLINE SIC PREPARED FROM CARBON-SATURATED SI MELT

2002 ◽  
Vol 16 (06n07) ◽  
pp. 1047-1051
Author(s):  
JIANPING MA ◽  
ZHIMING CHEN ◽  
GANG LU ◽  
MINGBIN YU ◽  
LIANMAO HANG ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Uv Light ◽  
X Ray Diffraction ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Composition And Structure ◽  
Light Excitation ◽  
Scanning Electron

Intense photoluminescence (PL) has been observed at room temperature from the polycrystalline SiC samples prepared from carbon-saturated Si melt at a temperature ranging from 1500 to 1650°C. Composition and structure of the samples have been confirmed by means of X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. PL measurements with 325 nm UV light excitation revealed that the room temperature PL spectrum of the samples consists of 3 luminescent bands, the peak energies of which are 2.38 eV, 2.77 eV and 3.06 eV, respectively. The 2.38 eV band is much stronger than the others. It is suggested that some extrinsic PL mechanisms associated with defect or interface states would be responsible to the intensive PL observed at room temperature.

scholarly journals Graphitic Nitrogen in Carbon Catalysts Important for the Reduction of Nitrite Revealed by 15N NMR Spectroscopy at Natural Abundance

2020 ◽  
Author(s):  
Zheng Chen ◽  
Aleksander Jaworski ◽  
Jianhong Chen ◽  
Tetyana Budnyak ◽  
Ireneusz Szewczyk ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Reduction Reaction ◽  
Nitrite Reduction ◽  
15N Nmr ◽  
Carbon Catalyst ◽  
X Ray ◽  
Wide Range ◽  
Alkaline Conditions

Metal-free nitrogen-doped carbon is considered as a green functional material, but the structural determination of the atomic positions of nitrogen remains challenging. We recently demonstrated that directly-excited solid state <sup>15</sup>N NMR (ssNMR) spectroscopy is a powerful tool for the determination of such positions in an N-doped carbon at natural <sup>15</sup>N isotope abundance. Here we present a green chemistry approach to the synthesis of N-doped carbon using cellulose as precursor, and a study of the catalytic properties and atomic structures of the related catalyst. The N-doped carbon (NH<sub>3</sub>) was obtained by oxidation of cellulose with HNO<sub>3</sub> followed by ammonolysis at 800°C. It had a N content of 6.5 wt.% and a surface area of 557 m<sup>2 </sup>g<sup>–1</sup>, and <sup>15</sup>N ssNMR spectroscopy provided evidence for graphitic nitrogen besides of regular pyrrolic and pyridinic nitrogen. This structure determination enabled probing the role of graphitic nitrogen for electrocatalytic reactions, such as the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and nitrite reduction reaction. The N-doped carbon catalyst (NH<sub>3</sub>) had higher electrocatalytic activities in OER and HER under alkaline conditions and a higher activity for nitrite reduction, as compared with a catalyst prepared by carbonization of the HNO<sub>3</sub>-treated cellulose in N<sub>2</sub>. The electrocatalytic selectivity for nitrite reduction of the N-doped carbon catalyst (NH<sub>3</sub>) was directly related to the graphitic nitrogen functions. Complementary structural analysis by means of <sup>13</sup>C and <sup>1</sup>H ssNMR, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and low-temperature N<sub>2 </sub>adsorption were preformed and provided support to the findings. The results show that directly-excited <sup>15</sup>N ssNMR at natural <sup>15</sup>N abundance is generally capable to provide information on N-doped carbon materials, and it is expected that the approach can be applied to a wide range of solids with an intermediate amount of N atoms.

Synthesis of Nanophase Noble Metal Systems Utilizing Porous Silicon

1996 ◽  
Vol 457 ◽  
Author(s):  
I. Coulthard ◽  
T. K. Sham
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Porous Silicon ◽  
Noble Metal ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Visible Range ◽  
X Ray ◽  
Metallic Salt ◽  
Scanning Electron

ABSTRACTApart from its well known ability to luminesce very intensely at room temperature in the visible range, porous silicon is also an effective reducing agent. We report the formation of several noble metal (Pd, Ag, Au, Pt) nanostructures by reductive dispersion of metal ions from aqueous solutions onto the surface of porous silicon. The nanophase systems produced by reductive deposition vary with the element deposited and the metallic salt utilized in the process. The resulting nanophase systems were studied using a variety of techniques including: scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and spectroscopie methods using synchrotron radiation.

scholarly journals In Situ and In Operando Techniques to Study Li-Ion and Solid-State Batteries: Micro to Atomic Level

Inorganics ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 85
Author(s):  
Maryam Golozar ◽  
Raynald Gauvin ◽  
Karim Zaghib
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Atomic Level ◽  
X Ray ◽  
In Situ Techniques ◽  
Transmission Electron ◽  
Wide Range ◽  
Li Ion

This work summarizes the most commonly used in situ techniques for the study of Li-ion batteries from the micro to the atomic level. In situ analysis has attracted a great deal of interest owing to its ability to provide a wide range of information about the cycling behavior of batteries from the beginning until the end of cycling. The in situ techniques that are covered are: X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), and Scanning Transmission Electron Microscopy (STEM). An optimized setup is required to be able to use any of these in situ techniques in battery applications. Depending on the type of data required, the available setup, and the type of battery, more than one of these techniques might be needed. This study organizes these techniques from the micro to the atomic level, and shows the types of data that can be obtained using these techniques, their advantages and their challenges, and possible strategies for overcoming these challenges.

scholarly journals Incorporating N Atoms into SnO2 Nanostructure as an Approach to Enhance Gas Sensing Property for Acetone

Nanomaterials ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 445 ◽  
Author(s):  
Xiangfeng Guan ◽  
Yongjing Wang ◽  
Peihui Luo ◽  
Yunlong Yu ◽  
Dagui Chen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Gas Sensor ◽  
Photoelectron Spectroscopy ◽  
High Performance ◽  
Gas Sensing ◽  
Diffuse Reflectance Spectroscopy ◽  
Limit Of Detection ◽  
Low Cost ◽  
X Ray ◽  
Sno2 Nanostructure

The development of high-performance acetone gas sensor is of great significance for environmental protection and personal safety. SnO2 has been intensively applied in chemical sensing areas, because of its low cost, high mobility of electrons, and good chemical stability. Herein, we incorporated nitrogen atoms into the SnO2 nanostructure by simple solvothermal and subsequent calcination to improve gas sensing property for acetone. The crystallization, morphology, element composition, and microstructure of as-prepared products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Electron paramagnetic resonance (EPR), Raman spectroscopy, UV–visible diffuse reflectance spectroscopy (UV–vis DRS), and the Brunauer–Emmett–Teller (BET) method. It has been found that N-incorporating resulted in decreased crystallite size, reduced band-gap width, increased surface oxygen vacancies, enlarged surface area, and narrowed pore size distribution. When evaluated as gas sensor, nitrogen-incorporated SnO2 nanostructure exhibited excellent sensitivity for acetone gas at the optimal operating temperature of 300 °C with high sensor response (Rair/Rgas − 1 = 357) and low limit of detection (7 ppb). The nitrogen-incorporated SnO2 gas sensor shows a good selectivity to acetone in the interfering gases of benzene, toluene, ethylbenzene, hydrogen, and methane. Furthermore, the possible gas-sensing mechanism of N-incorporated SnO2 toward acetone has been carefully discussed.

Carbon Dioxide Gas Sensor Using SAW Device Based on ZnO Film

2011 ◽  
Vol 135-136 ◽  
pp. 347-352 ◽  
Author(s):  
Chang Bao Wen ◽  
Yong Feng Ju ◽  
Wan Lin Li ◽  
Wen Zheng Sun ◽  
Xin Xu ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Gas Sensor ◽  
Side Lobe ◽  
Center Frequency ◽  
Zno Film ◽  
Co2 Gas ◽  
Response Characteristics ◽  
Carbon Dioxide Gas ◽  
Co2 Gas Sensor ◽  
Carbon Dioxide Co2

Carbon dioxide (CO2) gas sensor using surface acoustic wave (SAW) device based on Zinc oxide (ZnO) was developed and fabricated in this paper. The center frequency of SAW device is 203.528 MHz. The input and two output interdigital transducers (IDT) apodized by Morlet wavelet function can improve the side lobe rejection compared with uniform IDT. The ZnO film sensitive to CO2 gas was fabricated in measurement acoustic track of SAW device. Experiments results confirm that the CO2 gas sensor using SAW device based on ZnO film has good response characteristics to different concentrations CO2 gas. Furthermore, the CO2 gas sensor using SAW device based on ZnO film has good stability and linearity.

scholarly journals Получение нанокомпозитов МУНТ/MnO-=SUB=-2-x-=/SUB=-, МУНТ/MnO-=SUB=-2-x-=/SUB=-/CuO и исследования их газочувствительных свойств

2019 ◽  
Vol 61 (11) ◽  
pp. 2240
Author(s):  
Ю.А. Стенькин ◽  
В.В. Болотов ◽  
Д.В. Соколов ◽  
В.Е. Росликов ◽  
К.Е. Ивлев
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Copper Oxide ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Gas Sensing ◽  
Multiwalled Carbon ◽  
X Ray ◽  
P Type ◽  
Scanning Electron

Nanocomposites based on multiwalled carbon nanotubes (MWCNT) with manganese dioxide (MnO2-x) and copper oxide (CuO) were obtained and investigated. The morphology and elemental composition of MWCNT-layer and nanocomposites MWCNT/MnO2-х, MWCNT/MnO2-х/CuO were studied by scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The gas sensing response of MWCNT-layer and nanocomposites upon exposure to hydrogen sulfide (H2S) and nitrogen dioxide (NO2) was demonstrated at room temperature. Effect of increasing the conductivity of MWCNT-layer and nanocomposites upon exposure to NO2 indicates these nanomaterials have conductive of p-type. Copper oxide in nanocomposite significantly enhances the gas sensing response to H2S.

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