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Physics picture from neutron scattering study on Fe-based superconductors 被引量:1

Physics picture from neutron scattering study on Fe-based superconductors
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摘要 Neutron scattering, with its ability to measure the crystal structure, the magnetic order, and the structural and magnetic excitations, plays an active role in investigating various families of Fe-based high-Tc superconductors. Three different types of antiferromagnetic orders have been discovered in the Fe plane, but two of them cannot be explained by the spin-density-wave (SDW) mechanism of nesting Fermi surfaces. Noticing the close relation between antiferromagnetic order and lattice distortion in orbital ordering from previous studies on manganites and other oxides, we have advocated orbital ordering as the underlying common mechanism for the structural and antiferromagnetic transitions in the 1111, 122, and 11 parent compounds. We observe the coexistence of antiferromagnetic order and superconductivity in the (Ba,K)Fe2As2 system, when its phase separation is generally accepted. Optimal Tc is proposed to be controlled by the local FeAs4 tetrahedron from our investigation on the 1111 materials. The Bloch phase coherence of the Fermi liquid is found crucial to the occurrence of bulk superconductivity in iron chalcogenides of both the 11 and the 245 families. Iron chalcogenides carry a larger staggered magnetic moment (〉 2 tB/Fe) than that in iron pnictides (〈 1 .B/Fe) in the antiferromagnetic order. Normal state magnetic excitations in the 11 superconductor are of the itinerant nature while in the 245 superconductor the spin-waves of localized moments. The observation of superconducting resonance peak provides a crucial piece of information in current deliberation of the pairing symmetry in Fe-based superconductors. Neutron scattering, with its ability to measure the crystal structure, the magnetic order, and the structural and magnetic excitations, plays an active role in investigating various families of Fe-based high-Tc superconductors. Three different types of antiferromagnetic orders have been discovered in the Fe plane, but two of them cannot be explained by the spin-density-wave (SDW) mechanism of nesting Fermi surfaces. Noticing the close relation between antiferromagnetic order and lattice distortion in orbital ordering from previous studies on manganites and other oxides, we have advocated orbital ordering as the underlying common mechanism for the structural and antiferromagnetic transitions in the 1111, 122, and 11 parent compounds. We observe the coexistence of antiferromagnetic order and superconductivity in the (Ba,K)Fe2As2 system, when its phase separation is generally accepted. Optimal Tc is proposed to be controlled by the local FeAs4 tetrahedron from our investigation on the 1111 materials. The Bloch phase coherence of the Fermi liquid is found crucial to the occurrence of bulk superconductivity in iron chalcogenides of both the 11 and the 245 families. Iron chalcogenides carry a larger staggered magnetic moment (〉 2 tB/Fe) than that in iron pnictides (〈 1 .B/Fe) in the antiferromagnetic order. Normal state magnetic excitations in the 11 superconductor are of the itinerant nature while in the 245 superconductor the spin-waves of localized moments. The observation of superconducting resonance peak provides a crucial piece of information in current deliberation of the pairing symmetry in Fe-based superconductors.
作者 鲍威
机构地区 Department of Physics
出处 《Chinese Physics B》 SCIE EI CAS CSCD 2013年第8期90-97,共8页 中国物理B(英文版)
基金 supported by the National Basic Research Program of China(Grant Nos.2012CB921700 and 2011CBA00112) the National Natural Science Foundation of China(Grant Nos.11034012 and 11190024)
关键词 orbital ordering antiferromagnetic order EXCITATIONS structural transition orbital ordering, antiferromagnetic order, excitations, structural transition
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  • 1Kamihara Y, Watanabe T, Hirano M and Hosono H 2008 J. Am. Chem. Soc. 130 3296.
  • 2Kamihara Y, Hiramatsu H, Hirano M, Kawamura R, Yanagi H, Kamiya T and Hosono H 2006 J. Am. Chem. Soc. 128 10012.
  • 3Watanabe T, Yanagi H, Kamiya T, Kamihara Y and Hosono H 2007 lnorg. Chem. 46 7719.
  • 4Nagarajan R, Mazumdar C, Hossain Z, Dhar S K, Gopalakrishnan K V, Gupta L C, Godart C, Padalia B D and Vijayaraghavan R 1994 Phys. Rev. Lett. 72 274.
  • 5Cava R J, Takagi H, Batlogg B, Zandbergen H W, Krajewski J J, Peck J W F, van Dover R B, Felder R J, Siegrist T, Mizuhashi K, Lee J O, Eisaki H, Carter S A and Uchida S 1994 Nature 367 146.
  • 6Siegrist T, Zandbergen H W, Cava R J, Kra-jewski J J and Peck W F Jr 1994 Nature 367 254.
  • 7Canfield P C, Gammel P L and Bishop D J 1998 Phys. Today 51 40.
  • 8Chen X H, Wu T, Wu G, Liu R H, Chen H and Fang D F 2008 Nature 453 761.
  • 9Chen G F, Li Z, Wu D, Li G, Hu W Z, Dong .I, Zlaeng K Luo J L and Wang N L 2008 Phys. Rev. Lett. 100 247002.
  • 10Ren Z A, Lu W, Yang J, Yi W, Shen X L, Li Z C, Che G C, Dong X L, Sun L L, Zhou F and Zhao Z X 2008 Chin. Phys. Lett. 25 2215.

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