The role of H2O in enhancing hot filament assisted diamond growth at low temperatures

1997 ◽  
Vol 81 (3) ◽  
pp. 1536-1545 ◽  
Author(s):  
Z. Li Tolt ◽  
L. Heatherly ◽  
R. E. Clausing ◽  
C. S. Feigerle
1995 ◽  
Vol 10 (11) ◽  
pp. 2685-2688 ◽  
Author(s):  
Qijin Chen ◽  
Zhangda Lin

Diamond film was synthesized on thin Ti wafers (as thin as 40 μm) via hot filament chemical vapor deposition (HFCVD). The hydrogen embrittlement of the titanium substrate and the formation of a thick TiC interlayer were suppressed. A very low pressure (133 Pa) was employed to achieve high-density rapid nucleation and thus to suppress the formation of TiC. Oxygen was added to source gases to lower the growth temperature and therefore to slow down the hydrogenation of the thin Ti substrate. The role of the very low pressure during nucleation is discussed, providing insight into the nucleation mechanism of diamond on a titanium substrate. The as-grown diamond films were characterized by scanning electron microscopy (SEM), Raman spectroscopy, and x-ray analysis.


1992 ◽  
Vol 270 ◽  
Author(s):  
Ching-Hsong Wu ◽  
T. J. Potter ◽  
M. A. Tamor

ABSTRACTA mass spectrometric analysis of heavy hydrocarbons (HHCs) during hot-filament CVD diamond growth was performed together with in situ monitoring of the growth rate. Many HHCs were detected and tentatively identified. Of all HHCs studied, only diacetylene shows good correlation with the diamond growth rate under various deposition conditions. Its possible role is discussed.


1994 ◽  
Vol 339 ◽  
Author(s):  
Robin E. Rawles ◽  
Mark P. D'Evelyn

ABSTRACTGrowth and etch rates for diamond homoepitaxy have been measured in situ using Fizeau interferometry. Experiments were conducted in a hot-filament reactor using hydrogen, methane, and oxygen feed gases at a reactor pressure of 25 torr. The substrate temperature dependence for growth on diamond(lOO) was studied for 0.5% and 1% CH4 and 0–0.44% O2. Apparent activation energies of 17 and 5 kcal/mol were determined for growth from 0.5% and 1% CH4 in hydrogen, over the ranges of 700 – 1000 °C and 800 – 1050 °C, respectively. When a minimal amount of Oxygen was added to the feedstock, the growth-rate behavior was similar for that with pure methane. With greater amounts of added oxygen, growth rates were higher than those without Oxygen at low temperatures, proceeded through a maximum, and then decreased until etching was observed at high temperatures. Similar behavior was observed for growth from 1% CH4 with and without oxygen. We also measured the temperature dependence for etching of homoepitaxial diamond films in hydrogen with 0–0.1% O2, and observed etch rates of 0.01 – 0.1 microns/hr in the range of 950 – 1150 °C. We propose that oxygen facilitates diamond growth at low temperatures by enhancing the removal of both sp2- and sp3-bonded “errors” and/or by increasing the efficiency of carbon incorporation by roughening the diamond surface, and that these etching processes become dominant at high temperatures.


1994 ◽  
Vol 349 ◽  
Author(s):  
Evaldo. J. Corat ◽  
V. J. Trava-Airoldi ◽  
Nélia F. Leite ◽  
Angel F.V. Peña ◽  
Vítor Baranauskas

ABSTRACTIn this work we show that the addition of a small amount of CF4 to a regular CH4 -H2 gas mixture allows diamond growth at lower temperatures with reasonable growth rates. We used a hot filament assisted reactor and observed diamond growth with a substrate temperature as low as 390 ଌ. We present a comparative study for the growth dependence on substrate temperature with and without CF4 addition in the gas mixture. The growth rate is measured by post growth weighting with a micro balance. Raman spectroscopy, SEM and AFM images show the good quality of the films grown at low temperatures when CF4 is added to the feeding gas.


1998 ◽  
Vol 08 (PR7) ◽  
pp. Pr7-391-Pr7-399 ◽  
Author(s):  
S. Farhat ◽  
C. Findeling ◽  
F. Silva ◽  
K. Hassouni ◽  
A. Gicquel

2020 ◽  
Vol 65 (1) ◽  
pp. 28-41
Author(s):  
Marwa Aly Ahmed ◽  
Júlia Erdőssy ◽  
Viola Horváth

Multifunctional nanoparticles have been shown earlier to bind certain proteins with high affinity and the binding affinity could be enhanced by molecular imprinting of the target protein. In this work different initiator systems were used and compared during the synthesis of poly (N-isopropylacrylamide-co-acrylic acid-co-N-tert-butylacrylamide) nanoparticles with respect to their future applicability in molecular imprinting of lysozyme. The decomposition of ammonium persulfate initiator was initiated either thermally at 60 °C or by using redox activators, namely tetramethylethylenediamine or sodium bisulfite at low temperatures. Morphology differences in the resulting nanoparticles have been revealed using scanning electron microscopy and dynamic light scattering. During polymerization the conversion of each monomer was followed in time. Striking differences were demonstrated in the incorporation rate of acrylic acid between the tetramethylethylenediamine catalyzed initiation and the other systems. This led to a completely different nanoparticle microstructure the consequence of which was the distinctly lower lysozyme binding affinity. On the contrary, the use of sodium bisulfite activation resulted in similar nanoparticle structural homogeneity and protein binding affinity as the thermal initiation.


Materials ◽  
2021 ◽  
Vol 14 (2) ◽  
pp. 426
Author(s):  
Byeong-Kwan Song ◽  
Hwan-Young Kim ◽  
Kun-Su Kim ◽  
Jeong-Woo Yang ◽  
Nong-Moon Hwang

Although the growth rate of diamond increased with increasing methane concentration at the filament temperature of 2100 °C during a hot filament chemical vapor deposition (HFCVD), it decreased with increasing methane concentration from 1% CH4 –99% H2 to 3% CH4 –97% H2 at 1900 °C. We investigated this unusual dependence of the growth rate on the methane concentration, which might give insight into the growth mechanism of a diamond. One possibility would be that the high methane concentration increases the non-diamond phase, which is then etched faster by atomic hydrogen, resulting in a decrease in the growth rate with increasing methane concentration. At 3% CH4 –97% H2, the graphite was coated on the hot filament both at 1900 °C and 2100 °C. The graphite coating on the filament decreased the number of electrons emitted from the hot filament. The electron emission at 3% CH4 –97% H2 was 13 times less than that at 1% CH4 –99% H2 at the filament temperature of 1900 °C. The lower number of electrons at 3% CH4 –97% H2 was attributed to the formation of the non-diamond phase, which etched faster than diamond, resulting in a lower growth rate.


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