The chemical environment of Co sites in CoAl2O4 layers grown by metal-organic chemical vapor deposition has been investigated by X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD). It is shown that the air- or [O2 + H2O]-annealing at 500 °C of the layers deposited at low temperature induce a partial crystallization with the formation of (Co1-2ηAl2)(Co2Al2η)(Co 2ηAl2(1-η)))O4 spinel (η = 0.2-0.27). Nevertheless, slightly more than half of Co remains in an amorphous phase, and XAS data are consistent with the formation of a medium-range ordered Co3O4 phase, especially upon air-annealing. Layers grown at higher temperatures (600-650 °C) exhibit a similar but more complex structure, since the presence of an additional medium-range ordered phase (likely, CoAl2O4) is also revealed. The air-annealing at high temperature (800 °C) generates blue, almost completely crystalline, CoAl2O4 layers. Optical properties of deposited layers are discussed by referring to the outcomes of structural results. In particular, the optical absorption spectrum results negligibly affected by the presence of the amorphous phase, while absorptions present in the 300-500 nm range, responsible for the green layer color and evident in samples annealed in an oxidizing atmosphere or grown at high temperature, are likely caused by the octahedrally coordinated Co ions of the partially inverted spinel (Co;- 2ηAl2η)(Co2(1-η)Al 2(1-η))O4 -))O4 phase. Despite the XRD analysis that ultimately demonstrates the presence of octahedrally coordinated Co ions, whose oxidation state in the spinel phase is in majority Co(II), the occurrence of Co(III) species with an octahedral environment cannot be ruled out.

XAS and GIXRD Study of Co Sites in CoAl2O4 Layers Grown by MOCVD

CATTARUZZA, Elti;
2010-01-01

Abstract

The chemical environment of Co sites in CoAl2O4 layers grown by metal-organic chemical vapor deposition has been investigated by X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD). It is shown that the air- or [O2 + H2O]-annealing at 500 °C of the layers deposited at low temperature induce a partial crystallization with the formation of (Co1-2ηAl2)(Co2Al2η)(Co 2ηAl2(1-η)))O4 spinel (η = 0.2-0.27). Nevertheless, slightly more than half of Co remains in an amorphous phase, and XAS data are consistent with the formation of a medium-range ordered Co3O4 phase, especially upon air-annealing. Layers grown at higher temperatures (600-650 °C) exhibit a similar but more complex structure, since the presence of an additional medium-range ordered phase (likely, CoAl2O4) is also revealed. The air-annealing at high temperature (800 °C) generates blue, almost completely crystalline, CoAl2O4 layers. Optical properties of deposited layers are discussed by referring to the outcomes of structural results. In particular, the optical absorption spectrum results negligibly affected by the presence of the amorphous phase, while absorptions present in the 300-500 nm range, responsible for the green layer color and evident in samples annealed in an oxidizing atmosphere or grown at high temperature, are likely caused by the octahedrally coordinated Co ions of the partially inverted spinel (Co;- 2ηAl2η)(Co2(1-η)Al 2(1-η))O4 -))O4 phase. Despite the XRD analysis that ultimately demonstrates the presence of octahedrally coordinated Co ions, whose oxidation state in the spinel phase is in majority Co(II), the occurrence of Co(III) species with an octahedral environment cannot be ruled out.
2010
22
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/30437
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