Abstract

Both divalent and trivalent iron have been substituted into the zinc oxide lattice at levels up to about 2.5 atomic percent. Using enriched57Fe, Mössbauer studies indicate that either Fe2+or Fe3+may substitute for Zn2+at its normal lattice site. One spectrum indicative of Fe3+is observed when iron is substituted into zinc oxide under oxidizing conditions. However, two distinct spectra are found for Fe2+when iron is substituted into zinc oxide under reducing conditions. The quadrupole splitting of one of these Fe2+spectra shows an exceptionally high temperature dependence.

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