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Phase diagram and superconductivity at 58.1 K in {alpha}-FeAs free SmFeAsO1-xFx

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 Added by Masaya Fujioka
 Publication date 2013
  fields Physics
and research's language is English




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The Phase diagram of SmFeAsO1-xFx in terms of x is exhibited in this study. SmFeAsO1-xFx from x = 0 to x = 0.3 were prepared by low temperature sintering with slow cooling. The low temperature sintering suppresses the formation of the amorphous FeAs, which is inevitably produced as an impurity by using high temperature sintering. Moreover, slow cooling is effective to obtain the high fluorine concentration. The compositional change from feedstock composition is quite small after this synthesis. We can reproducibly observe a record superconducting transition for an iron based superconductor at 58.1 K. This achievement of a high superconducting transition is due to the success in a large amount of fluorine substitution. A shrinking of the a lattice parameter caused by fluorine substitution is observed and the substitutional rate of fluorine changes at x =0.16.



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We obtained amorphous-FeAs-free SmFeAsO1-xFx using a low temperature sintering with slow cooling. SmFeAsO1-xFx is sintered at 980 {deg}C for 40 hours and cooled slowly down to 600 {deg}C. The low temperature sintering suppresses the formation of amorphous FeAs, and the slow cooling introduces much fluorine into SmFeAsO1-xFx. The superconductivity of this sample appears at 57.8 K and the superconducting volume fraction reaches 96 %. To study the change of fluorine concentration during the cooling process, samples are quenched by water at 950 {deg}C, 900 {deg}C, 850 {deg}C, 800 {deg}C, 750 {deg}C and 700 {deg}C. It is found that fluorine is substituted not only at the maximum heating temperature but also during the cooling process. The low temperature sintering with slow cooling is very effective to obtain a homogeneous SmFeAsO1-xFx with high fluorine concentration.
We have studied the structural and electronic phase diagrams of CeFeAsO1-xFx and SmFeAsO1-xFx by a detailed analysis of muon spin relaxation experiments, synchrotron X-ray diffraction, Mossbauer spectroscopy, electrical resistivity, specific heat, and magnetic susceptibility measurements (Full abstract in the main document).
179 - Zhi-An Ren , Jie Yang , Wei Lu 2008
Since the discovery of copper oxide superconductor in 1986 [1], extensive efforts have been devoted to the search of new high-Tc superconducting materials, especially high-Tc systems other than cuprates. The recently discovered quaternary superconductor La[O1-xFx]FeAs with the superconducting critical transition Tc of 26 K [2], which has a much simple layered structure compared with cuprates, has attracted quick enthusiasm and is going to become a new high-Tc system [3-6]. Here we report the discovery of bulk superconductivity in the praseodymium-arsenide oxides Pr[O1-xFx]FeAs with an onset drop of resistivity as high as 52 K, and the unambiguous zero-resistivity and Meissner transition at low temperature, which will place these quaternary compounds to another high-Tc superconducting system explicitly.
118 - Zhi-An Ren , Wei Lu , Jie Yang 2008
Here we report the superconductivity in the iron-based oxyarsenide Sm[O1-xFx]FeAs, with the onset resistivity transition temperature at 55.0 K and Meissner transition at 54.6 K. This compound has the same crystal structure as LaOFeAs with shrunk crystal lattices, and becomes the superconductor with the highest critical temperature among all materials besides copper oxides.
269 - Wei Lu , Xiao-Li Shen , Jie Yang 2008
Here we report the superconductivity in the LaFeAsO1-xFx system prepared by high pressure synthesis. The highest onset superconducting transition temperature (Tc) in this La-based system is 41.0 K with the nominal composition of LaFeAsO1-xFx (x = 0.6), which is higher than that reported previously by ambient pressure synthesis. The increase of Tc can be attributed to the further shrinkage of crystal lattice that causes the stronger chemical pressure on the Fe-As plane, which is induced by the increased F-doping level under high pressure synthesis.
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