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1.
Lithographie Galvanoformung Abformung (LIGA) is a promising approach for fabrication of high aspect ratio 3D microactuator for dual-stage slider in hard disk drive. However, this approach involves practically challenging X-ray lithography and structural transfer processes. In this work, electrostatic MEMS actuator is developed based on a LIGA approach with cost-effective X-ray lithography and dry-film-transfer-to-PCB process. X-ray lithography is performed with X-ray mask based on lift-off sputtered Pb film on mylar substrate and photoresist application using casting-polishing method. High quality and high aspect ratio SU8 microstructures with inverted microactuator pattern have been achieved with the interdigit spacing of ~5 μm, vertical sidewall and a high aspect ratio of 29 by X-ray lithography using the low-cost Pb based X-ray mask. A new dry-film-transfer-to-PCB is employed by using low-cost dry film photoresist to transfer electroplated nickel from surface-treated chromium-coated glass substrate to printed circuit board (PCB) substrate. The dry film is subsequently released everywhere except anchor contacts of the electrostatic actuator structure. The fabricated actuator exhibits good actuation performance with high displacement at moderate operating voltage and suitably high resonance frequency. Therefore, the proposed fabrication process is a promising alternative to realize low-cost MEMS microactuator for industrial applications.  相似文献   
2.
Unloaded and 0.25–1.0 wt% Pt-loaded WO3 nanoparticles were synthesized by hydrothermal method using sodium tungstate dihydrate and sodium chloride as precursors in an acidic condition and impregnated using platinum acetylacetonate. Pt-loaded WO3 films on an Al2O3 substrate with interdigitated Au electrodes were prepared by spin-coating technique. The response of WO3 sensors with different Pt-loading concentrations was tested towards 0.01–1.0 vol% of H2 in air as a function of operating temperature (200–350 °C). The 1.0 wt% Pt-loaded WO3 sensing film showed the highest response of ∼2.16 × 104 to 1.0 vol% H2 at 250 °C. Therefore, an operating temperature of 250 °C was optimal for H2 detection. The responses of 1.0 wt% Pt-loaded WO3 sensing film to other flammable gases, including C2H5OH, C2H4 and CO, were considerably less, demonstrating Pt-loaded WO3 sensing film to be highly selective to H2.  相似文献   
3.
ZnO nanoparticles loaded with 0.2-2.0 at.% Pt have been successfully produced in a single step by flame spray pyrolysis (FSP) technique using zinc naphthenate and platinum(II) acetylacetonate, as precursors dissolved in xylene and their acetylene sensing characteristics have been investigated. The particle properties were analyzed by XRD, BET, TEM, SEM and EDS. Under the 5/5 (precursor/oxygen) flame condition, ZnO nanoparticles and nanorods were observed. The crystallite sizes of ZnO spherical and hexagonal particles were found to be ranging from 5 to 20 nm while ZnO nanorods were seen to be 5-20 nm in width and 20-40 nm in length. In addition, very fine Pt nanoparticles with diameter of ∼1 nm were uniformly deposited on the surface of ZnO particles. From gas-sensing characterization, acetylene sensing characteristics of ZnO nanoparticles is significantly improved as Pt content increased from 0 to 2  at.%. The 2 at.% Pt loaded ZnO sensing film showed an optimum C2H2 response of ∼836 at 1% acetylene concentration and 300 °C operating temperature. A low detection limit of 50 ppm was obtained at 300 °C operating temperature. In addition, Pt loaded ZnO sensing films exhibited good selectivity towards hydrogen, methane and carbon monoxide.  相似文献   
4.
This work presents a simple, low-cost and practical inkjet-printing technique for fabricating an innovative flexible gas sensor made of graphene–poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) composite film with high uniformity over a large area. An electronic ink prepared by graphene dispersion in PEDOT:PSS conducting polymer solution is inkjet-printed on a transparency substrate with prefabricated electrodes and investigated for ammonia (NH3) detection at room temperature. Transmission electron microscopy, Fourier transform infrared spectroscopy, UV–visible spectrometer and Raman characterizations confirm the presence of few-layer graphene in PEDOT:PSS polymer matrix and the present of π–π interactions between graphene and PEDOT:PSS. The ink-jet printed graphene–PEDOT:PSS gas sensor exhibits high response and high selectivity to NH3 in a low concentration range of 25–1000 ppm at room temperature. The attained gas-sensing performance may be attributed to the increased specific surface area by graphene and enhanced interactions between the sensing film and NH3 molecules via π electrons network. The NH3-sensing mechanisms of the flexible printed gas sensor based on chemisorbed oxygen interactions, direct charge transfers and swelling process are highlighted.  相似文献   
5.
Journal of Applied Electrochemistry - In this work, a screen-printed carbon paste electrode (SPCE) combined with multi-walled carbon nanotubes (MCNT) and graphene (GP) in different mixing ratios...  相似文献   
6.
An electronic nose (e-nose) system based on polymer/carboxylic-functionalized single-walled carbon nanotubes (SWNT-COOH) was developed for sensing various volatile amines. The SWNT-COOH dispersed in the matrix of different polymers; namely, polyvinyl chloride (PVC), cumene terminated polystyrene-co-maleic anhydride (cumene-PSMA), poly(styrenecomaleic acid) partial isobutyl/methyl mixed ester (PSE), and polyvinylpyrrolidon (PVP), were deposited on interdigitated gold electrodes to make the gas sensors. The response of these sensors to volatile amines was studied by both static and dynamic flow measurements. It was found that all sensors exhibited behaviors corresponding to Plateau-Bretano-Stevens law (R2 = 0.81 to 0.99) as the response to volatile amines. Real-world application was demonstrated by applying this e-nose to monitor the odor of sun-dried snakeskin gourami that was pre-processed by salting-preservation. This electronic nose can discriminate sun-dried fish odors with different stored days using a simple pattern recognition based on the principal component analysis (PCA).  相似文献   
7.
In this work, a new poly (3-hexylthiophene):1.00 mol% Au-loaded zinc oxide nanoparticles (P3HT:Au/ZnO NPs) hybrid sensor is developed and systematically studied for ammonia sensing applications. The 1.00 mol% Au/ZnO NPs were synthesized by a one-step flame spray pyrolysis (FSP) process and mixed with P3HT at different mixing ratios (1:1, 2:1, 3:1, 4:1, and 1:2) before drop casting on an Al2O3 substrate with interdigitated gold electrodes to form thick film sensors. Particle characterizations by X-ray diffraction (XRD), nitrogen adsorption analysis, and high-resolution transmission electron microscopy (HR-TEM) showed highly crystalline ZnO nanoparticles (5 to 15 nm) loaded with ultrafine Au nanoparticles (1 to 2 nm). Film characterizations by XRD, field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray (EDX) spectroscopy, and atomic force microscopy (AFM) revealed the presence of P3HT/ZnO mixed phases and porous nanoparticle structures in the composite thick film. The gas sensing properties of P3HT:1.00 mol% Au/ZnO NPs composite sensors were studied for reducing and oxidizing gases (NH3, C2H5OH, CO, H2S, NO2, and H2O) at room temperature. It was found that the composite film with 4:1 of P3HT:1.00 mol% Au/ZnO NPs exhibited the best NH3 sensing performances with high response (approximately 32 to 1,000 ppm of NH3), fast response time (4.2 s), and high selectivity at room temperature. Plausible mechanisms explaining the enhanced NH3 response by composite films were discussed.  相似文献   
8.
We have prepared SrTiO3/BaTiO3 multilayer film on alumina substrates by a sol-gel technique and investigated their response for sensing ethanol vapor. The surface morphology of the films were characterized by atomic force microscope (AFM) showing that the grain size of the films increase up to 40 nm as the annealing temperature increased to 1000 degrees C. The ethanol sensors based on SrTiO3/BaTiO3 thin films were fabricated by applying interdigitated gold electrodes by sputtering technique. The ethanol sensing characteristics of SrTiO3/BaTiO3 thin films were quantified by the change in resistance of the sensors when they were exposed to ethanol. The optimum operating tempearature of these sensors was found to be 350 degrees C. In addition, the film annealed at 1000 degrees C exhibited p-type gas sensing behavior with the best sensitivity of 30-100 for low ethanol concentration in the range of 100-1000 ppm.  相似文献   
9.
Unloaded ZnO and Nb/ZnO nanoparticles containing 0.25, 0.5 and 1 mol.% Nb were produced in a single step by flame-spray pyrolysis (FSP) technique. The nanoparticles were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The BET surface area (SSABET) of the nanoparticles was measured by nitrogen adsorption. FSP yielded small Nb particles attached to the surface of the supporting ZnO nanoparticles, indicating a high SSABET. The morphology and accurate size of the primary particles were further investigated by TEM. Nb/ZnO nanoparticles paste composed of ethyl cellulose and terpineol as binder and solvent respectively was coated on Al2O3 substrate interdigitated with gold electrodes to form thick films by spin coating technique. After the sensing tests, the morphology and the cross-section of sensing film were analyzed by SEM and EDS analyses. The influence on a low dynamic range of Nb concentration on NO2 response (0.1-4 ppm) of thick film sensor elements was studied at the operating temperatures ranging from 250 to 350 °C in the presence of dry air. The optimum Nb concentration was found be 0.5 mol.% and 0.5 mol.% Nb exhibited an optimum NO2 response of ∼1640 and a short response time (27 s) for NO2 concentration of 4 ppm at 300 °C.  相似文献   
10.
SnO2 nanoparticles loaded with 0.2–2 wt% Pt have successfully been synthesized in a single step by flame spray pyrolysis (FSP) and investigated for gas sensing towards hydrogen (H2). According to characterization results by X-ray diffraction, nitrogen adsorption, scanning/high resolution-transmission electron microscopy and analyses based on Hume-Rothery rules using atomic radii, crystal structure, electronegativities, and valency/oxidation states of Pt and Sn, it is conclusive that Pt is not solute in SnO2 crystal but forms nanoparticles loaded on SnO2 surface. H2 gas sensing was studied at 200–10,000 ppm and 150–350 °C in dry air. It was found that H2 response was enhanced by more than one order of magnitude with a small Pt loading concentration of 0.2 wt% but further increase of Pt loading amount resulted in deteriorated H2-sensing performance. The optimal SnO2 sensing film (0.2 wt% Pt-loaded SnO2, 20 μm in thickness) showed an optimum H2 response of ∼150.2 at 10,000 ppm and very short response time in a few seconds at a low optimal operating temperature of 200 °C. In addition, the response tended to increase linearly and the response times decreased drastically with increasing H2 concentration. Moreover, the selectivity against carbon monoxide (CO) and acetylene (C2H2) gases was also found to be considerably improved with the small amount of Pt loading. The H2 response dependence on Pt concentration can be explained based on the spillover mechanism, which is highly effective only when Pt catalyst is well-dispersed at the low Pt loading concentration of 0.2 wt%.  相似文献   
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