Issue 47, 2016

Ammonolysis of polycrystalline and amorphized gallium arsenide GaAs to polytype-specific nanopowders of gallium nitride GaN

Abstract

Convenient single-step N-for-As metathesis reactions of gallium arsenide GaAs with ammonia NH3 at temperatures in the range 650–950 °C for 6–90 hours afforded in this oxygen-free system high yields of pure nanocrystalline powders of the wide bandgap semiconductor gallium nitride GaN. High energy ball milling via noticeable amorphization of the monocrystalline cubic GaAs substrate enabled complete ammonolysis and nitride preparation at lower temperatures and shorter times relative to manual grinding. Under the applied conditions, all by-products were removed as volatiles affording pure GaN nanopowders. Reaction-controlled average crystallite sizes ranged from a few to a few tens of nanometers. When compared to the related ammonolysis reactions of cubic GaP and cubic GaSb which yielded, respectively, either the hexagonal polytype only or mixtures of mostly hexagonal with some cubic GaN polytypes, here, the nitride could be made both as solely hexagonal and as a mixture of two polytypes in a wide composition range. All this supports diverse reaction pathways which were found to be closely correlated with substrate grain size characteristics. The ball milled fine GaAs particles afforded only hexagonal or hexagonal GaN-enriched mixtures pointing to predominantly thermodynamic reaction control. Under similar conditions, the manually ground coarser GaAs particles yielded cubic GaN-enriched mixtures, instead, consistent with prevailing topochemical control.

Graphical abstract: Ammonolysis of polycrystalline and amorphized gallium arsenide GaAs to polytype-specific nanopowders of gallium nitride GaN

Supplementary files

Article information

Article type
Paper
Submitted
03 Mar 2016
Accepted
16 Apr 2016
First published
20 Apr 2016

RSC Adv., 2016,6, 41074-41086

Ammonolysis of polycrystalline and amorphized gallium arsenide GaAs to polytype-specific nanopowders of gallium nitride GaN

M. Drygaś, P. Jeleń, M. Radecka and J. F. Janik, RSC Adv., 2016, 6, 41074 DOI: 10.1039/C6RA05706C

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