TY - JOUR
T1 - Magnetism in Fe-based superconductors
AU - Lumsden, M. D.
AU - Christianson, A. D.
PY - 2010
Y1 - 2010
N2 - In this review, we present a summary of experimental studies of magnetism in Fe-based superconductors. The doping dependent phase diagram shows strong similarities to the generic phase diagram of the cuprates. Parent compounds exhibit magnetic order together with a structural phase transition, both of which are progressively suppressed with doping, allowing superconductivity to emerge. The stripe-like spin arrangement of Fe moments in the magnetically ordered state shows identical in-plane structure for the RFeAsO (R = rare earth) and AFe2As2 (A = Sr, Ca, Ba, Eu and K) parent compounds, notably different than the spin configuration of the cuprates. Interestingly, Fe1 + yTe orders with a different spin order despite having very similar Fermi surface topology. Studies of the spin dynamics of the parent compounds show that the interactions are best characterized as anisotropic three-dimensional interactions. Despite the room temperature tetragonal structure, analysis of the low temperature spin waves under the assumption of a Heisenberg Hamiltonian indicates strong in-plane anisotropy with a significant next-nearest-neighbor interaction. For the superconducting state, a resonance, localized in both wavevector and energy, is observed in the spin excitation spectrum as for the cuprates. This resonance is observed at a wavevector compatible with a Fermi surface nesting instability independent of the magnetic ordering of the relevant parent compound. The resonance energy (Er) scales with the superconducting transition temperature (TC) as E r ∼ 4.9kBTC, which is consistent with the canonical value of ∼ 5kBTC observed for the cuprates. Moreover, the relationship between the resonance energy and the superconducting gap, Δ, is similar to that observed for many unconventional superconductors (Er/2Δ ∼ 0.64).
AB - In this review, we present a summary of experimental studies of magnetism in Fe-based superconductors. The doping dependent phase diagram shows strong similarities to the generic phase diagram of the cuprates. Parent compounds exhibit magnetic order together with a structural phase transition, both of which are progressively suppressed with doping, allowing superconductivity to emerge. The stripe-like spin arrangement of Fe moments in the magnetically ordered state shows identical in-plane structure for the RFeAsO (R = rare earth) and AFe2As2 (A = Sr, Ca, Ba, Eu and K) parent compounds, notably different than the spin configuration of the cuprates. Interestingly, Fe1 + yTe orders with a different spin order despite having very similar Fermi surface topology. Studies of the spin dynamics of the parent compounds show that the interactions are best characterized as anisotropic three-dimensional interactions. Despite the room temperature tetragonal structure, analysis of the low temperature spin waves under the assumption of a Heisenberg Hamiltonian indicates strong in-plane anisotropy with a significant next-nearest-neighbor interaction. For the superconducting state, a resonance, localized in both wavevector and energy, is observed in the spin excitation spectrum as for the cuprates. This resonance is observed at a wavevector compatible with a Fermi surface nesting instability independent of the magnetic ordering of the relevant parent compound. The resonance energy (Er) scales with the superconducting transition temperature (TC) as E r ∼ 4.9kBTC, which is consistent with the canonical value of ∼ 5kBTC observed for the cuprates. Moreover, the relationship between the resonance energy and the superconducting gap, Δ, is similar to that observed for many unconventional superconductors (Er/2Δ ∼ 0.64).
UR - http://www.scopus.com/inward/record.url?scp=77956298177&partnerID=8YFLogxK
U2 - 10.1088/0953-8984/22/20/203203
DO - 10.1088/0953-8984/22/20/203203
M3 - Review article
AN - SCOPUS:77956298177
SN - 0953-8984
VL - 22
JO - Journal of Physics Condensed Matter
JF - Journal of Physics Condensed Matter
IS - 20
M1 - 203203
ER -