Novel Method for Controlling Nano Thin Coatings on Particulate Materials

1998 ◽  
Vol 526 ◽  
Author(s):  
J. Fitz-Gerald ◽  
S. Pennycook ◽  
H. Gao ◽  
V. Krishnamoorthy ◽  
J. Marcinka ◽  
...  

AbstractParticulate coatings have wide ranging applications in several new technologies such as flat-panel displays, sintering of advanced ceramics, rechargeable batteries, etc. In this paper, we show the feasibility of the pulsed laser ablation technique to make very thin, uniformly distributed and discrete coatings in particulate systems so that the properties of the core particles can be suitably modified. Presently, laser ablation techniques have been primarily applied to deposit thin films on flat substrate materials. To deposit discontinuous particulate coatings, the laser induced plume from the target comes in contact with an agitated bed of core particles. The pressure and nature of the background gas (inert or active) controls the cluster size of the nano particles in the laser plume. Experiments were conducted for laser deposition of Ag nano particles on Al2O3 and SiO2 core particles by pulsed excimer laser (wavelength = 248 nm and pulse duration = 25 nanosecond) irradiation of a Ag sputtering target The surface coverage and coating uniformities of the film were found to depend on the synthesis parameters (energy density, # laser pulses, gas pressure backfill gas, molecular weight) as well as the residence time of the core particles in the plume regime. The films were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), wavelength dispersive x-ray analysis (WDX), scanning transmission electron microscopy (STEM), and x-ray photoelectron spectroscopy (XPS).

1997 ◽  
Vol 501 ◽  
Author(s):  
J. Fitz-Gerald ◽  
R. K. Singh

ABSTRACTParticulate coatings have wide ranging applications in several new technologies such as flatpanel displays, sintering of advanced ceramics, rechargeable batteries, etc. In this paper, we show the feasibility of the pulsed laser ablation technique to make very thin, uniformly distributed and discrete coatings in particulate systems so that the properties of the core particles can be suitably modified. Presently, laser ablation techniques have been primarily applied to deposit thin films on flat substrate materials. To deposit discontinuous particulate coatings, the laser induced plume from the target comes in contact with an agitated bed of core particles (size 1–800μm). The pressure and nature of the background gas (inert or active) controls the cluster size of the particles in the laser plume. Experiments were conducted for laser deposition of silver particles on alumina core particles by excimer laser (wavelength = 248 nm and pulse duration = 25 nanosecond) irradiation of silver targets. The surface coverage and the coating of the film wasf found to depend on the laser parameters (energy density and number of laser pulses) as well as the residence time of the core particles in the plume regime. The films were characterized by wavelength and energy dispersive x-ray spectroscopy and x-ray photoelectron spectroscopy techniques.


2010 ◽  
Vol 148-149 ◽  
pp. 998-1002 ◽  
Author(s):  
Xiao Yun Chen ◽  
Hua Li ◽  
Yue Zeng Su ◽  
Zi Shan Huang ◽  
He Zhou Liu

Spinel CoFe2O4 nano-particles were synthesized by hydrothermal traditionally and Ethylene Glycol (EG) assisted hydrothermal process originally. The effects of reaction temperatures from 140°C to 200°C, different OH- provider and EG/water ratio on the nano-particles’ structure, morphology and magnetic properties of composition were studied by X-ray diffractometer (XRD), transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). The possible mechanism for the effects on the properties was also discussed in details. The results showed that NaAC as OH- provider and higher EG/water ratio in solvent were benefit for getting smaller CoFe2O4 nano-particles. And existence of EG is also important to remove the α-Fe2O3 phase.


2011 ◽  
Vol 688 ◽  
pp. 245-249 ◽  
Author(s):  
Zhi Qiang Wei ◽  
Xiao Yun Wang ◽  
Hua Yang

Special carbon encapsulated Fe core-shell nanoparticles with a size range of 15–40 nm were successfully prepared via confined arc plasma method. The composition, morphology, microstructure, specific surface area, particle size of the product by this process were characterized via X-ray diffraction (XRD), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM), X-ray energy dispersive spectrometry (XEDS) and BET N2adsorption. The experiment results shown that the carbon encapsulated Fe nanoparticles with clear core-shell structure, the core of the particles is body centered cubic (BCC) structure Fe, and the shell of the particles is disorder carbons. The particle size of the nanocapsules ranges from 15 to 40nm,with an averaged value about 30nm, the particles diameter of the core is about 16nm and the thickness of the shells is about 6-8 nm, and the specific surface area is 24 m2/g.


2005 ◽  
Vol 873 ◽  
Author(s):  
Mitsuhiro Okuda ◽  
Ichiro Yamashita ◽  
Kenji Iwahori ◽  
Hideyuki Yoshimura

AbstractIn2O3 nanoparticles were fabricated in the cavity of the cage-shaped protein, apoferritin by utilizing a quick chemical reaction of indium oxide. Horse spleen apoferritin in the solution of indium ions buffered at pH 9.5 was incubated for 30 minutes. The transmission electron microscopy (TEM) observation with aurothioglucose staining showed that cores were formed in the apoferritin cavity. The sizes of cores were regulated by the cavity size and their diameters were below 7nm. Energy dispersion X-ray analysis (EDX) indicated that indium was contained in the cores. The high-resolution TEM (HR-TEM) revealed that cores are single or poly crystalline and the lattice space was consistent with that of In2O3. These results confirmed that the In2O3 cores were successfully formed in the apoferritin cavity.


2009 ◽  
Vol 79-82 ◽  
pp. 373-376 ◽  
Author(s):  
Zhao Deng ◽  
Ying Dai ◽  
Hai Rui Liu ◽  
Wen Chen

Large scale BaTiO3 nanorods were successfully synthesized by a template method based on a precipitation process. The templates used in our method are H2Ti8O17 nanorods, which can be synthesized from K2Ti4O9 fibers. The unique process of the synthesis is BaC2O4•0.5H2O shell was coated on the 1-dimensional H2Ti8O17 nanorods (the core). The as-prepared products were characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results show that the BaTiO3 nanorods are ~100-300 nm in diameter and ~2-10 m in length. The process described provides a general route to fabricate this kind of perovskite 1-dimensional nanostructures, such as SrTiO3 and PbTiO3.


2017 ◽  
Vol 23 (3) ◽  
pp. 501-512 ◽  
Author(s):  
Sina Baier ◽  
Christian D. Damsgaard ◽  
Michael Klumpp ◽  
Juliane Reinhardt ◽  
Thomas Sheppard ◽  
...  

AbstractWhen using bifunctional core@shell catalysts, the stability of both the shell and core–shell interface is crucial for catalytic applications. In the present study, we elucidate the stability of a CuO/ZnO/Al2O3@ZSM-5 core@shell material, used for one-stage synthesis of dimethyl ether from synthesis gas. The catalyst stability was studied in a hierarchical manner by complementary environmental transmission electron microscopy (ETEM), scanning electron microscopy (SEM) andin situhard X-ray ptychography with a specially designedin situcell. Both reductive activation and reoxidation were applied. The core–shell interface was found to be stable during reducing and oxidizing treatment at 250°C as observed by ETEM andin situX-ray ptychography, although strong changes occurred in the core on a 10 nm scale due to the reduction of copper oxide to metallic copper particles. At 350°C,in situX-ray ptychography indicated the occurrence of structural changes also on theµm scale, i.e. the core material and parts of the shell undergo restructuring. Nevertheless, the crucial core–shell interface required for full bifunctionality appeared to remain stable. This study demonstrates the potential of these correlativein situmicroscopy techniques for hierarchically designed catalysts.


2002 ◽  
Vol 17 (9) ◽  
pp. 2197-2200 ◽  
Author(s):  
Juan Yang ◽  
Sen Mei ◽  
José M.F. Ferreira

Well-dispersed anatase and rutile nano-particles were prepared via hydrothermal treatment of tetrabutylammonium hydroxide-peptized and HNO3-peptized sols at 240 °C. A broad particle size distribution of anatase crystals was observed in the nonpeptized TiO2 species hydrothermally treated at 240 °C. X-ray diffraction and transmission electron microscopy, as well as zeta potential measurement, were used to characterize the particles. The formation of the well-dispersed anatase and rutile particles from the peptized samples could be attributed to (i) homogeneous distribution of the component in the peptized sols, and (ii) the high long-range electrostatic forces between particles in the presence of both peptizers, which were not present in the nonpeptized samples. This work provided a new way to prepare nano-crystals of titania.


1994 ◽  
Vol 354 ◽  
Author(s):  
Zhong-Min Ren ◽  
Yuan-Cheng Du ◽  
Xia-Xing Xiong ◽  
Jia-Da Wu ◽  
Zhi-Feng Ying ◽  
...  

AbstractCN1 thin films have been synthesized by ion-beam-assisted laser ablation of graphite. Films with N-concentration of 45% are obtained, indicated by high energy backseattering spectrum (HEBS). Raman and X-ray photoelectron spectroscopy (XPS) data confirm the existence of carbon-nitrogen bonds. Polycrystallites beta-CjNi structure has been detected in the amorphous matrix of the films, as indicated by transmission electron microscopy (TEM) and electron diffraction. Qualitative tests indicate that the films are relatively hard and adhesive.


Author(s):  
S. Fujishiro

The mechanical properties of three titanium alloys (Ti-7Mo-3Al, Ti-7Mo- 3Cu and Ti-7Mo-3Ta) were evaluated as function of: 1) Solutionizing in the beta field and aging, 2) Thermal Mechanical Processing in the beta field and aging, 3) Solutionizing in the alpha + beta field and aging. The samples were isothermally aged in the temperature range 300° to 700*C for 4 to 24 hours, followed by a water quench. Transmission electron microscopy and X-ray method were used to identify the phase formed. All three alloys solutionized at 1050°C (beta field) transformed to martensitic alpha (alpha prime) upon being water quenched. Despite this heavily strained alpha prime, which is characterized by microtwins the tensile strength of the as-quenched alloys is relatively low and the elongation is as high as 30%.


Author(s):  
R. Gronsky

The phenomenon of clustering in Al-Ag alloys has been extensively studied since the early work of Guinierl, wherein the pre-precipitation state was characterized as an assembly of spherical, ordered, silver-rich G.P. zones. Subsequent x-ray and TEM investigations yielded results in general agreement with this model. However, serious discrepancies were later revealed by the detailed x-ray diffraction - based computer simulations of Gragg and Cohen, i.e., the silver-rich clusters were instead octahedral in shape and fully disordered, atleast below 170°C. The object of the present investigation is to examine directly the structural characteristics of G.P. zones in Al-Ag by high resolution transmission electron microscopy.


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