Precise Determination of Thermal Expansion Coefficients Observed in 4H-SiC Single Crystals

2006 ◽  
Vol 527-529 ◽  
pp. 699-702 ◽  
Author(s):  
Masashi Nakabayashi ◽  
Tatsuo Fujimoto ◽  
Masakazu Katsuno ◽  
Noboru Ohtani

The coefficient of thermal expansion (CTE) of SiC single crystals is important, in particular, for both designing device assembly and controlling stress distributions in heteroepitaxial thin film structures grown onto SiC substrates. We have performed very precise measurements of the CTEs for SiC single crystals comprising of single 4H polytype PVT-grown in NIPPON Steel Corporation for a temperature range from 123 K to 473 K using a laser interferometry method. This method allows us to directly measure the temperature dependent variation in thermal expansion of the crystal volume with much higher accuracy, and enables us to straightforwardly obtain practical information of CTE data. Furthermore in order to discuss the CTE behavior for a wider temperature range the CTEs at higher temperatures up to 1573 K have been also measured using dilatometer method. The CTE obtained for a nitrogen-doped 4H-SiC single crystal increases continuously from 0.8 ppm/K to 3.1 ppm/K for temperatures of 273 K and 423 K respectively, and further increases to 5.4 ppm/K at 1273 K. We conclude from our data that the CTE variations are likely to be almost independent of the crystal axis directions of SiC from 123 K up to 1573 K.

1965 ◽  
Vol 43 (7) ◽  
pp. 1328-1333 ◽  
Author(s):  
D. A. Channing ◽  
S. Weintroub

The linear thermal expansion coefficients αψ of two single crystals of Zn of orientations ψ = 10.8° and 63.9 ° with the hexad axis were measured over the temperature range of about 20–270 °K using an absolute Fizeau optical interference technique. The two principal coefficients, [Formula: see text] and [Formula: see text], corresponding to ψ = 0° and 90 ° respectively, were calculated from the Voigt relation, and their values are compared with previously reported experimental data. Above 60 °K there is good agreement with previous work, and below 60 °K the results confirm, in general, the data obtained by McCammon and White. The Grüneisen parameter γ is essentially constant at about 2.1 in the range 100–270 °K, but below 100 °K γ rises appreciably with decreasing temperature and reaches the value of about 3.5 at 20 °K.


1992 ◽  
Vol 181 (1-2) ◽  
pp. 293-298 ◽  
Author(s):  
Y. Uwatoko ◽  
H. Okita ◽  
G. Oomi ◽  
I. Umehara ◽  
Y. Ōnuki

2018 ◽  
Vol 52 (27) ◽  
pp. 3745-3758 ◽  
Author(s):  
Amin Bahrami ◽  
Niloofar Soltani ◽  
Martin I Pech-Canul ◽  
Shaghayegh Soltani ◽  
Luis A González ◽  
...  

In this study, wettability behavior of B4C substrate as well as B4C/crystalline rice husk ash and B4C/amorphous rice husk ash substrates with two aluminum alloys were studied. The electrical resistivity, thermal expansion coefficients, and thermal diffusivity of bilayer Al/B4C/rice husk ash composite fabricated by one-step pressureless infiltration were measured and the obtained data were systemically analyzed using the Taguchi method and analysis of variance. Boron carbide substrates after addition of amorphous or crystalline rice husk ash display good wettability with molten aluminum alloys. The results show that, electrical resistivity of Al/B4C/rice husk ash composites is mainly influenced by initial preform porosity, while the coefficient of thermal expansion of composites is determined by the chemical composition of infiltrated alloys. The measured values for coefficient of thermal expansion (10.5 × 10−6/℃) and electrical resistivity (0.60 × 10−5 Ω.m) of Al/B4C/rice husk ash composites, fabricated according to analysis of variance's optimal conditions are in good agreement with those of the projected values (11.02 × 10−6/℃ and 0.65 × 10−5 Ω.m, respectively). The difference between the corresponding values obtained from verification tests and projected values, for electrical resistivity and coefficient of thermal expansion are less than 5%. Finally, as a material selection approach, the strengths and weaknesses of the composites have been graphed in the form of radar diagrams.


2018 ◽  
Vol 281 ◽  
pp. 169-174
Author(s):  
Yang Wang ◽  
Yuan Yuan Song ◽  
Yuan Yuan Zhou ◽  
Lu Ping Yang ◽  
Fu Tian Liu

Low thermal expansion ceramics have been widely applied in multiple fields. In this paper, a series of low thermal expansion ceramics SrZr4-xTix(PO4)6 was prepared and characterized. The SrZr4-xTix(PO4)6 ceramics could be well sintered in the temperature range of 1400~1500 °C. The effect of the addition of Ti substituting Zr and the sintering temperature was studied. The Ceramic with x =0.1 sintered at 1450 °C, the SrZr4-xTix(PO4)6 had a high relative density. The thermal expansion coefficients were about 3.301×10-6 °C-1. It was demonstrated that the microstructure of the SrZr4-xTix(PO4)6 could be altered by adding varying amount of Ti to tailor the thermophysical properties of the material.


2008 ◽  
Vol 368-372 ◽  
pp. 1662-1664 ◽  
Author(s):  
X.L. Xiao ◽  
M.M. Wu ◽  
J. Peng ◽  
Y.Z. Cheng ◽  
Zhong Bo Hu

Compounds Yb2Mo3O12 and Lu2Mo3O12 were prepared by conventional solid-state reaction. Their crystal structures and thermal expansion properties were investigated. It was found that Yb2Mo3O12 and Lu2Mo3O12 adopt orthorhombic structure and show negative thermal expansion (NTE) in the temperature range of 200-800 °C. Their a-axis and c-axis exhibit stronger contraction in the temperature range of 200-800 °C, while b-axis slightly expands in the temperature range of 200-300 °C and then contracts in the temperature range of 300-800 °C. The linear thermal expansion coefficients al of Yb2Mo3O12 and Lu2Mo3O12 are −5.17 × 10−6 °C−1 and −5.67 × 10−6 °C−1, respectively.


1986 ◽  
Vol 108 (3) ◽  
pp. 270-274 ◽  
Author(s):  
C. N. Chu ◽  
N. Saka ◽  
N. P. Suh

The coefficient of thermal expansion (CTE) of a hot pressed Ta16W18O94 which was produced from Ta2O5 and WO3 powders was found to be −1.52×10−6 K−1 in the temperature range 180–330 K. Using the Ta16W18O94 and Super Invar powders, 50:50 volume percent metal-ceramic composites were made by the powder metallurgy techniques. When the mixture of constituent powders was hot pressed at 1123 K for 10 minutes, a CTE of 1.1 × 10−6 K−1 was obtained in the temperature range 140–420 K.


1995 ◽  
Vol 73 (4) ◽  
pp. 513-521 ◽  
Author(s):  
Darek Michalski ◽  
Mary Anne White ◽  
Pradip K. Bakshi ◽  
T. Stanley Cameron ◽  
Ian Swainson

The crystal structures of hexakis(phenylthio)benzene (HPTB) and its CBr4 clathrate have been determined by single crystal X-ray diffraction data collected at T = 18 °C and refined to final Rw of 0.036 and 0.047, respectively. Pure HPTB is triclinic, space group [Formula: see text] (No. 2), with a = 9.589(2) Å, b = 10.256(1) Å, c = 10.645(2) Å, α = 68.42(1)°, β = 76.92(2)°, γ = 65.52(1)°, and Z = 1. The CBr4 clathrate of HPTB is rhombohedral, space group [Formula: see text] (No. 148), with a = 14.327(4) Å, b = 20.666(8) Å, and Z = 3. The host–guest mole ratio of HPTB–CBr4 is 1:2. Neutron powder diffraction was carried out on powders of both compounds in the temperature range 25 K < T < 295 K. Thermal expansion coefficients were determined for HPTB and HPTB–CBr4 over this temperature range. Keywords: thermal expansion, crystal structure, clathrate.


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