scholarly journals Micropipes in SiC Single Crystal Observed by Molten KOH Etching

Materials ◽  
2021 ◽  
Vol 14 (19) ◽  
pp. 5890
Author(s):  
Hejing Wang ◽  
Jinying Yu ◽  
Guojie Hu ◽  
Yan Peng ◽  
Xuejian Xie ◽  
...  

Micropipe, a “killer” defect in SiC crystals, severely hampers the outstanding performance of SiC-based devices. In this paper, the etching behavior of micropipes in 4H-SiC and 6H-SiC wafers was studied using the molten KOH etching method. The spectra of 4H-SiC and 6H-SiC crystals containing micropipes were examined using Raman scattering. A new Raman peak accompanying micropipes located near −784 cm−1 was observed, which may have been induced by polymorphic transformation during the etching process in the area of micropipe etch pits. This feature may provide a new way to distinguish micropipes from other defects. In addition, the preferable etching conditions for distinguishing micropipes from threading screw dislocations (TSDs) was determined using laser confocal microscopy, scanning electron microscopy (SEM) and optical microscopy. Meanwhile, the micropipe etching pits were classified into two types based on their morphology and formation mechanism.

2021 ◽  
Vol 63 (9) ◽  
pp. 1340
Author(s):  
Н.А. Иванов ◽  
С.А. Небогин ◽  
С.С. Колесников ◽  
Л.И. Брюквина

It is investigated the thermal etching of LiF and MgF2 crystals with cobalt and nickel impurities by means of scanning electron microscopy and atomic force microscopy with using decorating. It is shown that impurity inclusions leave the crystal from dislocations. The differences between of thermal etching in vacuum and air atmosphere take place. The crystallographic oriented terraced etch pits are formed after exit of impurities from dislocations. The square thermal etch pits are formed after thermal etching at 750°C in air. The surface impurity nanoscale film is formed at thermal etching. The oxidation of surface impurities observed at thermal etching in air atmosphere or in residual air atmosphere.


2019 ◽  
Vol 13 (4) ◽  
pp. 587-598 ◽  
Author(s):  
Maya Schnabel‐Lubovsky ◽  
Olga Kossover ◽  
Sonia Melino ◽  
Francesca Nanni ◽  
Yeshayahu Talmon ◽  
...  

2002 ◽  
Vol 16 (28n29) ◽  
pp. 4484-4486
Author(s):  
YUESHENG XU ◽  
CHUNLING ZHANG ◽  
LEI TANG ◽  
CAICHI LIU ◽  
JINGCHEN HAO

The micro-defects in semi-insulating gallium arsenide (SI-GaAs) were investigated by means of chemical etching (ultrasonic aided Abtahams-Buiocchi etching, melting KOH etching), transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The experimental results showed that the micro-defects in SI-GaAs are micro-precipitates of As with the size of microns. Micro-defects and dislocations have strong interaction, dislocations absorb the micro-defects and micro-defects decorate on the dislocations.


2020 ◽  
Author(s):  
Srinivas Ramachandra ◽  
Abdulla Abdal-hay ◽  
Pingping Han ◽  
Ryan Lee ◽  
Saso Ivanovski

<p><strong>Introduction</strong>: Biofilms are 3-dimensional (3D) aggregates of microorganisms that are associated with a wide range of diseases. Although there have been several studies investigating biofilm formation on two-dimensional substrates, the use of 3D substrates may result in more representative and clinically relevant models. Accordingly, the aim of this study was to compare the growth of biofilms in the 3D substrates against biofilms grown in 2D substrates.<br /><strong>Material and Methods:</strong> Two grams of medical grade polycaprolactone (PCL) were loaded into a plastic Luer-lock 3 ml syringe and a 23G needle was used as a spinneret. The syringe was placed in a melt electro-writing (MEW) device to obtain fine fibers under controlled parameters. The 3-dimensional MEW PCL scaffolds were manufactured and characterised with an overall thickness of ~ 0.8 mm, with ~ 15 μm diameter fibers and ordered pore sizes of either 100 or 250 µm. PCL films employed as 2D substrates were manufactured by dissolving 10 gms of PCL in 100 ml chloroform and stirred for 3 h to obtain a transparent solution. Then, the solution was cast in glass petri dishes and dried to remove all organic solvents. In addition, commercial hydroxyapatite discs were also used as 2D controls. Unstimulated saliva from six healthy donors (gingival health) were used to grow biofilms. The formed biofilms were assessed at day 4, day 7 and day 10 using crystal violet assay, confocal microscopy, scanning electron microscopy and next-generation 16s sequencing.<br /><strong>Results:</strong> The results demonstrates that 3D PCL scaffolds dramatically enhanced biofilm biomass and thickness growth compared to that of the 2D controls. Confocal microscopy of biofilms at day 4 stained with SYTO 9 and propidium iodide showed thickness of biofilms in 2D substrates were 39 µm and 81µm for hydroxyapatite discs and PCL films, respectively. Biofilms in 3D substrates were 250 µm and 338 µm for MEW PCL 100µm pore size and MEW PCL 250 µm pore size, respectively. Similar results were noticed at day 7 and day 10. Scanning electron microscopy showed biofilm bridges formed over the fibers of the MEW scaffolds. Pilot trials of next generation sequencing detected similar taxa in biofilms formed in 3D scaffolds compared to that of 2D substrates.<br /><strong>Discussion:</strong> We have successfully investigated a 3D biofilm growth model using 3D medical grade PCL scaffolds. Thicker biofilms can be conveniently grown using this inexpensive static model. This will facilitate 3D microbial community studies that are more clinically relevant and improve our understanding of biofilm-associated disease processes.</p> <p> </p>


2006 ◽  
Vol 911 ◽  
Author(s):  
Hui Chen ◽  
Guan Wang ◽  
Yi Chen ◽  
Xiaoting Jia ◽  
Jie Bai ◽  
...  

AbstractCarrot-like defects in a 7&#61616; off-cut (from [0001] toward <1-210> direction) 4H-SiC wafer with a 36μm thick 4H-SiC epilayer have been investigated using Nomarski optical microscopy, synchrotron white beam x-ray topography (SWBXT), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). X-ray topographs confirm that threading screw dislocations are often associated with the carrots. Cross-sectional TEM observation confirms that a prismatic stacking fault exists below the carrot. This fault was found to show contrast in all observed diffraction geometries except for g=0004. A model for the mechanism of formation of this type of defect during epitaxial growth is proposed.


2018 ◽  
Vol 17 ◽  
pp. 153601211878732 ◽  
Author(s):  
Joseph E. Kobes ◽  
George I. Georgiev ◽  
Anthony V. Louis ◽  
Isen A. Calderon ◽  
Eriko S. Yoshimaru ◽  
...  

Reseeding of decellularized organ scaffolds with a patient’s own cells has promise for eliminating graft versus host disease. This study investigated whether ultrasound imaging or magnetic resonance imaging (MRI) can track the reseeding of murine liver scaffolds with silica-labeled or iron-labeled liver hepatocytes. Mesoporous silica particles were created using the Stöber method, loaded with Alexa Flour 647 fluorophore, and conjugated with protamine sulfate, glutamine, and glycine. Fluorescent iron oxide particles were obtained from a commercial source. Liver cells from donor mice were loaded with the silica particles or iron oxide particles. Donor livers were decellularized and reperfused with silica-labeled or iron-labeled cells. The reseeded livers were longitudinally analyzed with ultrasound imaging and MRI. Liver biopsies were imaged with confocal microscopy and scanning electron microscopy. Ultrasound imaging had a detection limit of 0.28 mg/mL, while MRI had a lower detection limit of 0.08 mg/mL based on particle weight. The silica-loaded cells proliferated at a slower rate compared to iron-loaded cells. Ultrasound imaging, MRI, and confocal microscopy underestimated cell numbers relative to scanning electron microscopy. Ultrasound imaging had the greatest underestimation due to coarse resolution compared to the other imaging modalities. Despite this underestimation, both ultrasound imaging and MRI successfully tracked the longitudinal recellularization of liver scaffolds.


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