Boron doping: B/H/C/O gas-phase chemistry; H atom density dependences on pressure and wire temperature; puzzles regarding the gas-surface mechanism

Experimental and modeling studies of the gas-phase chemistry occurring in dilute, hot filament (HF) activated B 2H 6/CH 4/H 2 gas mixtures appropriate for growth of boron-doped diamond are reported. The results of two-dimensional modeling of heat and mass transfer processes and the B/H/C chemistry p...

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Veröffentlicht in:Thin solid films 2011-05, Vol.519 (14), p.4421-4425
Hauptverfasser: Mankelevich, Yuri A., Ashfold, Michael N.R., Comerford, Dane W., Ma, Jie, Richley, James C.
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Sprache:eng
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Zusammenfassung:Experimental and modeling studies of the gas-phase chemistry occurring in dilute, hot filament (HF) activated B 2H 6/CH 4/H 2 gas mixtures appropriate for growth of boron-doped diamond are reported. The results of two-dimensional modeling of heat and mass transfer processes and the B/H/C chemistry prevailing in such HF activated gas mixtures (supplemented by reactions involving trace O 2 present as air impurity in the process gas mixture) are discussed and compared with measurements of B atom densities as functions of the hot wire temperature T w and distance from the wire. Most of the B 2H 6 molecules that diffuse from the cool, near-wall regions into the hot, near wire region are thermally decomposed (yielding two BH 3 molecules as primary products) and then converted into various ‘active’ B-containing species like B, BH and BH 2 — some of which are able to accommodate into the growing diamond film. H-shifting reactions BH x + H ↔ BH x − 1 + H 2 enable rapid inter-conversion between the various BH x ( x = 0–3) species and the BH x source is limited by diffusional transfer of B 2H 6. H atoms play several key roles — e.g. activating the process gas mixture, and driving inter-conversions between the various H x B y C z O z′ species. We show that the T w and gas pressure dependences of the H atom production rate (by H 2 dissociation on the HF surface) can be accommodated by a simple gas-surface reaction model.
ISSN:0040-6090
1879-2731
DOI:10.1016/j.tsf.2011.01.328