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000020184 084__ $$2WoS$$aPhysics, Condensed Matter
000020184 1001_ $$0P:(DE-HGF)0$$aMishra, S.K.$$b0
000020184 245__ $$aPressure dependence of the low-temperature crystal structure and phase transition behavior of CaFeAsF and SrFeAsF: A synchrotron x-ray diffraction study
000020184 260__ $$aCollege Park, Md.$$bAPS$$c2011
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000020184 440_0 $$04919$$aPhysical Review B$$v84$$x1098-0121$$y22
000020184 500__ $$aR. Mittal and S. K. Mishra thank the Department of Science and Technology (DST), India for providing financial support to carry out synchrotron x-ray diffraction at the European Synchrotron Radiation Facility, Grenoble, France.
000020184 520__ $$aWe report systematic investigation of high pressure crystal structures and structural phase transition up to 46 GPa in CaFeAsF and 40 GPa in SrFeAsF at 40 K using powder synchrotron x-ray diffraction experiments and Rietveld analysis of the diffraction data. We find that CaFeAsF undergoes orthorhombic to monoclinic phase transition at P-c = 13.7 GPa while increasing pressure. SrFeAsF exhibits coexistence of orthorhombic and monoclinic phases over a large pressure range from 9 to 39 GPa. The coexistence of the two phases indicates that the transition is of first order in nature. Unlike in the 122 compounds (BaFe2As2 and CaFe2As2), we do not find any collapse tetragonal transition. The transition to a lower symmetry phase (orthorhombic to monoclinic) in 1111 compounds under pressure is in contrast with the transition to a high symmetry phase (orthorhombic to tetragonal) in 122-type compounds. On heating from 40 K at high pressure, CaFeAsF undergoes monoclinic to tetragonal phase transition around 25 GPa and 200 K. Further, it does not show any post-tetragonal phase transition and remains in the tetragonal phase up to 25 GPa at 300 K. The dP(c)/dT is found to be positive for the CaFeAsF and CaFe2As2, however the same was not found in case of BaFe2As2.
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000020184 7001_ $$0P:(DE-HGF)0$$aChaplot, S. L.$$b2
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