Reduction of carbon impurities in aluminium nitride from time-resolved chemical vapour deposition using trimethylaluminum

Author(s):  
Polla Rouf ◽  
Pitsiri Sukkaew ◽  
Lars Ojamäe ◽  
Henrik Pedersen

<p>Aluminium nitride (AlN) is a semiconductor with a wide range of applications from light emitting diodes to high frequency transistors. Electronic grade AlN is routinely deposited at 1000 °C by chemical vapour deposition (CVD) using trimethylaluminium (TMA) and NH<sub>3</sub> while low temperature CVD routes to high quality AlN are scarce and suffer from high levels of carbon impurities in the film. We report on an ALD-like CVD approach with time-resolved precursor supply where thermally induced desorption of methyl groups from the AlN surface is enhanced by the addition of an extra pulse, H<sub>2</sub>, N<sub>2</sub> or Ar between the TMA and NH<sub>3</sub> pulses. The enhanced desorption allowed deposition of AlN films with carbon content of 1 at. % at 480 °C. Kinetic- and quantum chemical modelling suggest that the extra pulse between TMA and NH<sub>3</sub> prevents re-adsorption of desorbing methyl groups terminating the AlN surface after the TMA pulse. </p>

2020 ◽  
Author(s):  
Polla Rouf ◽  
Pitsiri Sukkaew ◽  
Adam Hultqvist ◽  
Tobias Törndahl ◽  
Lars Ojamäe ◽  
...  

Aluminium nitride (AlN) is a semiconductor with a wide range of applications from light emitting diodes to high frequency transistors. Electronic grade AlN is routinely deposited at 1000 °C by chemical vapour deposition (CVD) using trimethylaluminium (TMA) and NH<sub>3</sub> while low temperature CVD routes to high quality AlN are scares and suffer from high levels of carbon impurities in the film. We report on an ALD-like CVD approach with time-resolved precursor supply where thermally induced desorption of methyl groups from the AlN surface is enhanced by the addition of an extra pulse, H<sub>2</sub>, N<sub>2</sub> or Ar between the TMA and NH<sub>3</sub> pulses. The enhanced desorption allowed deposition of AlN films with carbon content of 1 at. % at 480 °C. Mass spectrometry combined with kinetic- and quantum chemical modelling show that the extra pulse between TMA and NH<sub>3</sub> enhances the desorption and prevents re-adsorption of the methyl groups, terminating the AlN surface after the TMA pulse. The surface methyl groups are found to desorb as CH<sub>3</sub>, CH<sub>4</sub> and C<sub>2</sub>H<sub>x</sub>.


2020 ◽  
Author(s):  
Polla Rouf ◽  
Pitsiri Sukkaew ◽  
Lars Ojamäe ◽  
Henrik Pedersen

<p>Aluminium nitride (AlN) is a semiconductor with a wide range of applications from light emitting diodes to high frequency transistors. Electronic grade AlN is routinely deposited at 1000 °C by chemical vapour deposition (CVD) using trimethylaluminium (TMA) and NH<sub>3</sub> while low temperature CVD routes to high quality AlN are scarce and suffer from high levels of carbon impurities in the film. We report on an ALD-like CVD approach with time-resolved precursor supply where thermally induced desorption of methyl groups from the AlN surface is enhanced by the addition of an extra pulse, H<sub>2</sub>, N<sub>2</sub> or Ar between the TMA and NH<sub>3</sub> pulses. The enhanced desorption allowed deposition of AlN films with carbon content of 1 at. % at 480 °C. Kinetic- and quantum chemical modelling suggest that the extra pulse between TMA and NH<sub>3</sub> prevents re-adsorption of desorbing methyl groups terminating the AlN surface after the TMA pulse. </p>


1994 ◽  
Vol 29 (16) ◽  
pp. 4314-4318 ◽  
Author(s):  
A. H. Khan ◽  
M. F. Odeh ◽  
J. M. Meese ◽  
E. M. Charlson ◽  
E. J. Charlson ◽  
...  

1989 ◽  
Vol 94 (2) ◽  
pp. 387-391 ◽  
Author(s):  
Hideaki Itoh ◽  
Hisashi Morikawa ◽  
Kohzoh Sugiyama

2011 ◽  
Vol 700 ◽  
pp. 112-115
Author(s):  
Mark Alexander Bissett ◽  
Anders Jack Barlow ◽  
Joe George Shapter ◽  
Jamie Scott Quinton

Simple and up-scalable production of carbon nanotubes (CNTs) still remains difficult with current production methods. Plasma enhanced chemical vapour deposition (PECVD) provides an excellent method for producing high purity and large amounts of carbon nanotubes. This work demonstrates how PECVD can be used to tailor the required properties in the resultant nanotubes produced. By altering only one of the growth variables the resultant CNTs can be altered from single-walled to multi-walled. This was achieved by altering the growth temperature from 450-650°C, altering the growth time and altering the underlying catalyst and supporting layer. High purity SWCNT and MWCNT could be produced and easily distinguished leading to a wide range of applications.


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