Magnetic properties of sol-gel synthesized C-doped ZnO nanoparticles

ZnO doping with Carbon (C-doped ZnO) materials were prepared by sol-gel technique following with a heat treatment process. Single phase of Wurtzite crystal structure of ZnO was concluded via x-ray diffraction (XRD) with a large amount of excess C tracking by energy dispersive X-ray spectroscopy (EDX...

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Veröffentlicht in:Journal of alloys and compounds 2016-05, Vol.668, p.87-90
Hauptverfasser: Dung, Nguyen Duc, Son, Cao Thai, Loc, Pham Vu, Cuong, Nguyen Huu, Kien, Pham The, Huy, Pham Thanh, Ha, Ngo Ngoc
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Sprache:eng
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Zusammenfassung:ZnO doping with Carbon (C-doped ZnO) materials were prepared by sol-gel technique following with a heat treatment process. Single phase of Wurtzite crystal structure of ZnO was concluded via x-ray diffraction (XRD) with a large amount of excess C tracking by energy dispersive X-ray spectroscopy (EDX) analysis. Two types of ZnO crystals (twinning particles) with different grain sizes and shapes were identified via scanning electron microscopy (FE-SEM). The first type has a smaller grain size of about 20 nm and hexagonal shape. And the second type has a larger grain size of about 80–120 nm and round shape. C substitutions of both Zn and O sites to form C–O and C–Zn bonds were conclusively confirmed via x-ray photoelectron spectroscope (XPS). Experimental evidences for the co-existence of different ferromagnetic phases in the materials are reported and discussed. Two Curie points at high temperatures (>500 °C) are presented. A metamagnetic transition was observed at magnetic field H = 19.2 kOe which was related to the co-existence of ferromagnetic phases. These involve in the formation of twinning C-doped ZnO nanoparticles. •Formation of sol-gel prepared single phase wurtzite ZnO nanoparticles.•Two morphological C-doped ZnO nanoparticles of different grain sizes.•The room temperature ferromagnetism.•An abnormal metamagnetic transition at magnetic field H = 19.2 kOe.•Two different Curie points (TC) at 500–600 °C.
ISSN:0925-8388
1873-4669
DOI:10.1016/j.jallcom.2016.01.208