The controlled synthesis of ZnO at
the micro- and nanoscale has
been the focus of significant research due to its importance in electrical
and optoelectronic applications, and the potential of tuning its properties
at the crystal formation stage. We present a detailed study of ZnO
growth processes which supports and consolidates previous findings
and gives a clearer understanding of the mechanism of ZnO formation.
The influence of synthesis conditions on ZnO formation was investigated
by comparison of two different growth routes (Zn(CH3COO)2–NH3 and Zn(NO3)2·6H2O−HMTA) both known to result in the formation of wurtzite
structured, twinned hexagonal rods of ZnO. The identities of the solid
phases formed and supernatants were confirmed by data from SEM, XRD,
FTIR, XPS, TGA, and ICP-OES analysis; giving insight into the involvement
of multistep pathways. In both cases, reaction takes place via intermediates
known as layered basic zinc salts (LBZs) which only later transform
to the oxide phase. In the ZnAc2–NH3 system,
crystal growth evolves as Zn(CH3COO)2 →
LBZA (A: acetate) → ZnO through a dissolution/reprecipitation
process, with the formation of an additional product identified as
LBZAC (C: carbonate). In contrast, in the Zn(NO3)2·6H2O−HMTA system, solid-phase transformation
occurs as Zn(NO3)2·6H2O →
LBZN (N: nitrate) → ZnO with no evidence of dissolution. Similar
comprehensive studies can be applied to other solid-state processes
to further advance functional materials design.