Enhanced Desorption of Surface Methyl Groups in Time-Resolved Chemical Vapour Deposition of Aluminium Nitride from Trimethylaluminum

28 February 2020, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

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 NH3 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, H2, N2 or Ar between the TMA and NH3 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 NH3 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 CH3, CH4 and C2Hx.

Keywords

AlN
CVD
ALD
surface reaction

Supplementary materials

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