2010
DOI: 10.1016/j.solidstatesciences.2009.11.018
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Structural variations and cation distributions in Mn3−xCoxO4 (0≤x≤3) dense ceramics using neutron diffraction data

Abstract: OATAO is an open access repository that collects the work of Toulouse researchers and makes it freely available over the web where possible. This is an author -deposited version published in: http://oatao.univ-toulouse.fr/ Eprints ID: 3829

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Cited by 102 publications
(117 citation statements)
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“…According to our previous studies performed on ceramics of similar compositions (Bordeneuve, Rousset, Tenailleau, Guillemet-Fritsch, 2010b) . However, the reduction processes are not fully completed at the highest temperature of TGA measurements (T = 1300 °C) and it is not observed for CoMn 2 O 4 nanopowders, in accordance with previous results obtained on ceramics (Bordeneuve et al, 2010a). The dark Co 3-x Mn x O 4 (x = 1, 1.5, 2) nanoparticles display absorbance of light in the UV and early visible spectra, as shown in Figure 6.…”
Section: Resultssupporting
confidence: 89%
See 1 more Smart Citation
“…According to our previous studies performed on ceramics of similar compositions (Bordeneuve, Rousset, Tenailleau, Guillemet-Fritsch, 2010b) . However, the reduction processes are not fully completed at the highest temperature of TGA measurements (T = 1300 °C) and it is not observed for CoMn 2 O 4 nanopowders, in accordance with previous results obtained on ceramics (Bordeneuve et al, 2010a). The dark Co 3-x Mn x O 4 (x = 1, 1.5, 2) nanoparticles display absorbance of light in the UV and early visible spectra, as shown in Figure 6.…”
Section: Resultssupporting
confidence: 89%
“…A scheme of agglomerate and a dark colloidal suspension of Co 2 MnO 4 are shown in insets of Figure 1 to illustrate the synthetic products. (Bordeneuve et al, 2010a). At room temperature, it is known that Mn 3-x Co x O 4 undergoes a symmetry transition at x ~ 1.7 where a peak splitting is observed for some peaks of the cubic phase as the symmetry is lowered (Aukrust & Muan, 1964).…”
Section: Resultsmentioning
confidence: 99%
“…Although neutron powder diffraction data were only recorded to demonstrate a neutron diffraction inert cryoprotectant, the collected data of hydrogenated L-(-)-ephedrine hemihydrate could be solved and refined directly without an X-ray model. However, most applications of neutron powder diffraction are carried out to follow changes in the crystal structure [78], e.g., when atoms and molecules are absorbed [79,80] or the crystal structure changes due to strain [81,82]. Neutron powder data retain the advantage of the strong scattering by particular nuclei, especially deuterium and of course does not suffer from the sporadic availability of the very large single crystals needed for single crystal neutron work.…”
Section: Neutron Diffractionmentioning
confidence: 99%
“…Consequently, the real structure is tetragonal rather than cubic. [14,15]. For a spinel structure rich in Mn 3+ , net distortion of these octahedral sites could lead to a unit cell transformation from cubic to tetragonal if the amount of Mn 3+ in these sites is high enough [16].…”
Section: Resultsmentioning
confidence: 99%