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• W1981296661 abstract "In this paper, the magnetic properties of p-type Zn <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>1-x</sub> Mn <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>x</sub> O powders are reported. This are prepared from the decomposition of an oxalate precursor Zn <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>1-x</sub> Mn <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>x</sub> C <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>2</sub> O <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>4</sub> <sup xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>.</sup> H <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>2</sub> O. The oxalate precursor is obtained by coprecipitation of 50 ml of a 0.4mol/L aqueous solution of Zn and Mn acetates and the same volume of a 0.4 mol/L solution of oxalic acid. The mixed solution is stirred for 2h at room temperature. We added CH <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>3</sub> COONH <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>4</sub> and In(NO <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>3</sub> ) <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>3</sub> <sup xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>.</sup> H <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>2</sub> O as p-type doped source (Zn:N:In=l:3:0.05 mol) to the solution with addition 3h stirring. The precipitate is then washed with distilled water and dried in air. The white powders obtained are then annealed in N <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>2</sub> at 500-800 K for 2h and finally turned moss yellow powder samples. The structure of the powder samples are studied by X-ray diffraction (XRD). All the observed lines from the XRD patterns show the ZnO structure without any hint of an impurity phase. With the increase of x, the peak position of Zn <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>1-x</sub> Mn <sub xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>x</sub> O shifts towards lower angles and the lattice constants a and c increase linearly, which means that the Mn <sup xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>2+</sup> replaces well the Zn <sup xmlns:mml=http://www.w3.org/1998/Math/MathML xmlns:xlink=http://www.w3.org/1999/xlink>2+</sup> to occupy the 2b crystallographic site." @default.
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• W1981296661 date "2010-10-01" @default.
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• W1981296661 title "The magnetic properties of p-type Zn<inf>1−x</inf>Mn<inf>x</inf>O achieved by co-precipitation technique" @default.
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• W1981296661 doi "https://doi.org/10.1109/ivesc.2010.5644190" @default.
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