An Introduction to Fe-based superconductors

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Presentation transcript:

An Introduction to Fe-based superconductors Yuen Yiu University of Tennessee, Department of Physics and Astronomy Knoxville, TN 37922

Overview Brief history: Discovery and progress Material variations: 4 types of material: “1111”, “122”, “111” and “11” [10] Experiments and physical properties: Transport properties, magnetic properties, crystal structures, phase diagram Theoretical models

Brief History Reported by Kamihara et al. on 19rd March 2008, paper titled “Iron based superconductor La[O1-xFx]FeAsO with Tc=26K” [12] has been cited for 1,117 times as of 4th March 2010! Only non-cuprate high Tc superconductors (Tc>20K) Very popular at the moment: There is at least one presentation session EVERY DAY at the upcoming APS March meeting Table 1 Maximum Tc in each RFeAs(O1-xFx). The F concentration x, which gives the maximum Tc is shown [10]

Material variations RFeAsO “1111” family “122” family RFeAsO (R can be but not limited to: Ce, Pr, Nd, Sm, La) Superconductivity induced by Oxygen site electron doping (usually with F), or simply creating oxygen deficiency Iron site electron doping has also been reported AFe2As2 (A = Ba, Sr, Ca, etc.) SC induced by A-site doping with monovalent B+ (i.e. K, Cs, Na, etc.) Iron site doping with Co has been reported

Material variations Li-deficient LiFeAs superconducts “111” family (?) “11” family Li-deficient LiFeAs superconducts Superconductivity very sensitive to sample preparation [10] Parent compounds superconducts (?) Not as popular Simplest structure Se-deficient FeSe superconducts up to 8K [10] NOTE: the PARENT COMPOUNDS DO NOT SUPERCONDUCT UNDER AMBIENT PRESSURE!!!

Crystal structure “1111”: layers of FeAs and LaO “122”: layers of FeAs and K/Sr “111”: layers of FeAs and Li “11”: layers of FeSe Figure 1 (a) Crystal structure of LaOFeAs; [2] (b) Crystal structure of (K/Sr)Fe2As2 and (Cs/Sr)Fe2As2 [2]

Sample Synthesis EXAMPLE: Polycrystals: conventional solid state reaction. PrFeAsO: start with PrAs, Fe2O3 and Fe powders. Ground up stoichiometric mixtures in glovebox, pressed into pellets, sealed in silica tubes in argon, and then heated at 1200oC for 30 hrs. [11] Figure 2 A picture of what PrFeAsO powder looks like

Transport properties Figure 3 Temperature dependence of electrical resistivity of LaFeAsO1-xFx. The inset is a phase diagram constructed with the data. [9] Broad peak at T~150K is generally associated with the SDW phase transition The transition is suppressed and shifted to a lower temperature as doping level increases Superconductivity emerges at x=0.03

Neutron Powder Diffraction Peak splitting: tetragonal- orthorhombic structural transition (Extra) Magnetic peaks found at 5K Figure 4, 5, 6 (left) NPD data for PrFeAsO [5]; (center) Lattice parameter v. Temperature data showing structural transition [Yiu Y. et al., unpublished]; (right) Lattice parameters v. doping level [8]

Behold! The General “1111” Phase Diagram Suppress the following and SC will EMERGE! Structural transition, magnetic phase transition (Naïve, experimentalist point of view) Can be done by chemical doping or applied pressure Figure 7 The structural, magnetic, and superconducting phase diagram of PrFeAsO1−xFx [3]

Behold! The General “122” Phase Diagram Superconductivity coexists with antiferromagnetism!?? Interesting… Figure 8 The structural, magnetic, and superconducting phase diagram of BaFe2- xCoxAs2 a member from the122 family [14]

Theoretical models Non BCS theory of superconductivity!? Works suggesting the s±-pairing state Unconventional and mediated by (nesting-related) antiferromagnetic spin fluctuations [13] First example of multigap superconductivity with a discontinuous sign change between the bands [13] Similar but different from the famous superconducting MgB2 [13] No common consensus yet

Conclusions “Fe-based superconductors” is a new and exciting field 4 different types of crystal structure found in this group The parent compounds do not superconduct, but undergo a structural distortion, a SDW phase transition and magnetic ordering instead. These transitions can be suppressed by chemical doping or applied pressure (unexplored today) and superconductivity will emerge No universally accepted theoretical model yet

References [1] Liu R. H. et al, Phy. Review Letters, 101, 087001 (2008) [2] Sasmal K. et al, Phy. Review Letters, 101, 107007 (2008) [3] Rotundu C. R. et al, Phy. Review B, 80, 144517 (2009) [4] Ren Z. A, Materials Research Innovations 12, 1 (2008) [5] Zhao J. et al, Phy. Review B, 78, 132504 (2008) [6] Qi Y. P. et al, Phy. Review B, 80, 054502 (2009) [7] Wang et al, Phy, Review B, 78, 054521 (2009) [8] Han F. et al, Phy, Review B, 80 024506 (2009) [9] Dong J. et al, Europhys. Letter, 83, 27006 (2008) [10] Ishida k. et al, Journal of the Phy. Socity of Japan, 78, 062001 (2009) [11] McGuire M. A. et al, Journal of Solid State Chemistry, 182, 8, p 2326-2331 (2009) [12] Kamihara et al., Journal of American Chemical Society, 130, 11, p. 3296+ (2008) [13] Mazin I. I. et al., Phys. Rev. Lett., 101 057003 (2008) [14] Wang X. F. et al., arXiv:0811.2920.