Numerical Simulation and Experimental Analysis on the Crystal Growth of Excimer-Laser Crystallization of a-Si Film

Author(s):  
Long-Sun Chao ◽  
Yu-Ru Chen ◽  
Hsiun-Chang Peng

In this work, the excimer-laser-induced crystallization of amorphous silicon (a-Si) films was investigated numerically and experimentally. The basic structure is an a-Si film on a glass substrate. This study had investigated the effects of irradiating energy density on the grain size and structure by scanning electron microscopy (SEM). In the surface microstructure analysis of the laser-irradiated area, the critical fluences (full-melt threshold, FMT) between the partial melting and complete melting regimes can be found by applying scanning electron microscopy. An efficient two-dimensional numerical model is carried out to predict the critical fluences (FMT) and the transient temperature distribution during the laser processing. Numerical analysis of the temperature profile showed that a temperature drop occurred at the center of melted zone immediately after laser irradiation. From the analysis of temperature responses, the FMT obtained from the simulation results of the proposed model agree fairly well with those from the experimental data reported in the literature and acquired in this research. Furthermore, the grain growth of the poly-Si was studied by the grain observation of the cross section and its corresponding numerical simulation. The cross-sectional grain structure of the resulting poly-Si film was observed with different laser intensities. The grain sizes decreased with increasing irradiating energy intensity in the partial melting regime. From the surface observation, the grain distribution was uniform and most of the grain has a single crystallographic direction. The average grain size had the biggest value at FMT. But some super large grains occurred and combined with more than one crystallographic direction when the film obtained sufficiently high energy intensities that was closed or over the FMT. The grain distribution was not uniform. The super large gain was around the small grain size. The modified cellular automation method (MCA) was used to simulate the grain growth two-dimensionally and explain the grain development during the solidification process. The grain morphology of the numerical simulation was satisfied with the experimental observation. From the analysis of the grain growth, this model was able to simulate the undercooling effect and grain growth phenomenon and fitted for the experimental grain observation in the excimer-laser-induced crystallization.

2011 ◽  
Vol 492 ◽  
pp. 97-101
Author(s):  
Yuan Fei Gao ◽  
Zhao Hui Huang ◽  
Kai Chen ◽  
Ming Hao Fang ◽  
Yang Gai Liu

A WTi(C,N)-06 cemented carbide with TaC and NbC is studied as the research objective in this paper. The phase composition of the cemented carbide was analyzed by using XRD method, and the microstructure of the cemented carbide was studied and evaluated by using optical microscopy and scanning electron microscopy. According to the comparison with a general-grained cemented carbide, the addition of TaC and NbC can suppress the grain growth of WC crystal, and it is also good for improving mechanism performance. The average grain size of WTi(C,N)-06 cemented carbide is 2.1μm, density 12.9g/cm3, hardness 74HRC, and bending strength 2378MPa.


2007 ◽  
Vol 561-565 ◽  
pp. 2163-2166 ◽  
Author(s):  
H.Z. Abdullah ◽  
Charles C. Sorrell

Rutile nano-powders were suspended in a solution of acetylacetone and iodine. The suspensions were electrophoretically deposited on titanium foil at a voltage range of 5-30 V over times of 5-120 s. The dried tapes then were sintered at 800°C for 2 h in flowing argon. Both the green and fired tapes were examined by field emission scanning electron microscopy, optical microscopy, X-ray diffraction, and Raman microspectroscopy. The thickness of the films depended on the voltage and the time of deposition. The sintered microstructures depended significantly on the thickness of the film, which was a function the proximity to the Ti/TiO2 interface. The interface is critical to the microstructure because it acts as the source of defect formation, which enhances sintering, grain growth, and grain facetting.


1994 ◽  
Vol 9 (2) ◽  
pp. 286-291 ◽  
Author(s):  
Kunsong Ma ◽  
Alain C. Pierre

Bi—(Pb)—Sr—Ca—Cu—O superconductors were synthesized by sol-gel processing from nitrates by complexation with citric acid. Their grain growth and sintering above 800 °C were studied by Scanning Electron Microscopy (SEM) and Brunauer, Emmett, Teller (BET) porosimetry. The sintering was limited by anisotropic grain growth, and microcracks in 2212 phase grains were created due to the formation of 2223 phase.


2012 ◽  
Vol 496 ◽  
pp. 379-382
Author(s):  
Rui Song Yang ◽  
Ming Tian Li ◽  
Chun Hai Liu ◽  
Xue Jun Cui ◽  
Yong Zhong Jin

The Cu0.81Ni0.19 has been synthesized directly from elemental powder of nickel and copper by mechanical alloying. The alloyed Cu0.81Ni0.19 alloy powders are prepared by milling of 8h. The grain size calculated by Scherrer equation of the NiCu alloy decreased with the increasing of milling time. The end-product was analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM)


2018 ◽  
Vol 281 ◽  
pp. 156-162
Author(s):  
Wang Nian Zhang ◽  
Xi Tang Wang ◽  
Zhou Fu Wang

The influence of the light burning temperature on the sintering property of nature dolomite has been investigated by two-step sintering process in the temperature range 1500 °C to 1600 °C. The resulting bulk densities and apparent porosities of the sintered dolomite samples were examined, and analyzing the sintered dolomite by scanning electron microscopy and X-ray diffraction were performed. The results showed light burned at 850 °C for 3 h, the main phases of the dolomite with 3-5 grain size were MgO, CaO and little CaCO3, and then fired at 1600 °C,the density of sintering dolomite reached to 3.38 g/cm3, the apparent property was 1.2 %, the size of MgO grain up to 3.75 μm . However when dolomite light burned at 1050 °C for 3 h, the main phases were MgO and CaO, and then fired at 1600 °C,the density of sintering dolomite only was 3.30 g/cm3, the apparent property was 2.3 %, the size of MgO only was 3.05 μm .


2011 ◽  
Vol 686 ◽  
pp. 348-354 ◽  
Author(s):  
Shu Tao Xiong ◽  
Fu Sheng Pan ◽  
Bin Jiang ◽  
Xiao Ke Li

In the present work, Al-Ca metallic compound was prepared in Mg-Ca alloys and the effects of Al-Ca metallic compound and different Al/Ca values on the grain refinement of Mg-Ca alloys were investigated by scanning electron microscopy and X-ray diffraction, and the mechanism of grain refinement of Mg-Ca alloys was discussed. The results showed that the grain size of Mg-0.5Ca alloy was obviously reduced from 550μm to 230μm due to the addition of Al. Al2Ca phase existed in these alloys and its morphology evolved from granular to rod-like. It is regarded as the main factor for the grain refinement.


2007 ◽  
Vol 539-543 ◽  
pp. 3568-3573
Author(s):  
H. Kumagai ◽  
M. Shibata ◽  
Tomokazu Moritani ◽  
Takao Kozakai ◽  
Minoru Doi ◽  
...  

When the Al/Ge/SiO2 bilayer films are annealed in-situ in a scanning electron microscope (SEM) at the temperatures lower than the crystallization temperature of amorphous Ge itself, the so-called metal-mediated-crystallization (MMC) takes place. In the course of MMC, crystalline Ge aggregates (Ge clusters) form in the bilayer films, which results in the formation and the evolution of impressive fractal patterns with branching on the free surface. In-situ SEM observations of annealed Al/Ge/SiO2 bilayer films indicate that the grain size of polycrystalline Al-layer influences the nucleation of Ge clusters and hence of fractal patterns. For the bilayer films containing larger Al grains, the nucleation rate of fractal patterns (Ge clusters) is faster and the number of patterns is larger.


2008 ◽  
Vol 8 (8) ◽  
pp. 4127-4131 ◽  
Author(s):  
G. S. Okram ◽  
Kh. Namrata Devi ◽  
H. Sanatombi ◽  
Ajay Soni ◽  
V. Ganesan ◽  
...  

Nanocrystalline nickel powders were prepared with grain size 'd' in the range 40–100 nm diameters through polyol method. X-ray diffraction (XRD), scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used for characterization. XRD of the prepared samples consistently matched with standard fcc structure of nickel without any impurity peak. Detailed analysis and calculations using Scherrer equation for (111) peak revealed systematic increase in line width and peak shifting towards lower diffraction 2θ angles with decrease in nickel to ethylene glycol mole ratio. Different values of d estimated from various peaks of each sample suggested associated microstrains in the nanograins. Values of d estimated from X-ray diffraction patterns were compared with those obtained from atomic force microscopy and scanning electron microscopy results, and discussed. Observed lattice expansion is explained, on the basis of a theoretical model of linear elasticity.


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