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Room temperature magnetization in Co-doped anatase phase of TiO2
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Fysiska sektionen, Institutionen för fysik och astronomi.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Tekniska sektionen, Institutionen för teknikvetenskaper, Fasta tillståndets fysik.
Vise andre og tillknytning
2013 (engelsk)Inngår i: European Physical Journal: Applied physics, ISSN 1286-0042, E-ISSN 1286-0050, Vol. 61, nr 1, s. 10601-Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

CoxTi1-xO2 films were deposited by spray pyrolysis technique on Si(1 0 0) substrates at 475 degrees C. A hydro-alcoholic solution containing titanium (iv) isopropoxide and Co(NO3)(2) with various Co doping levels from x = 0-0.015 in solution was used as spray solution. Grazing incident angle of X-ray diffraction illustrates that the CoxTi1-xO2 films are single phase and polycrystal with mixed orientations. Study of surface morphology of the films by atomic force microscope reveals that the annealing atmosphere does not significantly affect the grain size and the microstructure of the films. This study provides further insight into the importance of annealing atmosphere on magnetization of the films. Room temperature magneto-optical Kerr measurement was employed in polar mode. A hysteresis loop and a paramagnetic behavior have been recorded for samples annealed in H-2 ambient gas and air, respectively. Chemical composition analysis by X-ray photo-electron spectroscopy showed that Co atoms are bounded to oxygen and no metallic clusters are present. Moreover, it indicates the formation of high spin Co2+ for the sample x = 0.008 annealed in H-2 ambient gas. The origin of magnetization can be attributed to the contribution of oxygen vacancies in the spin polarization of the structure.

sted, utgiver, år, opplag, sider
2013. Vol. 61, nr 1, s. 10601-
HSV kategori
Forskningsprogram
Teknisk fysik med inriktning mot fasta tillståndets fysik
Identifikatorer
URN: urn:nbn:se:uu:diva-196079DOI: 10.1051/epjap/2012120243ISI: 000314352800009OAI: oai:DiVA.org:uu-196079DiVA, id: diva2:609275
Tilgjengelig fra: 2013-03-05 Laget: 2013-03-04 Sist oppdatert: 2017-12-06bibliografisk kontrollert

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