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Based on the minimum two-orbital model and the phase diagram recently proposed by Tai et al. (Europhys. Lett. textbf{103}, 67001(2013)) for both electron- and hole-doped 122 iron-based superconducting compounds, we use the Bogoliubov-de Gennes equations to perform a comprehensive investigation of the evolution of the Fermi surface (FS) topology in the presence of the collinear spin-density-wave (SDW) order as the doping is changed. In the parent compound, the ground state is the SDW order, where the FS is not completely gapped, and two types of Dirac cones, one electron-doped and the other hole-doped emerge in the magnetic Brillouin zone. Our findings are qualitatively consistent with recent angle-resolved photoemission spectroscopy and magneto-resistivity measurements. We also examine the FS evolution of both electron- and hole-doped cases and compare them with measurements, as well as with those obtained by other model Hamiltonians.
Based on a minimal two-orbital model [Tai {it et al.}, Europhys. Lett. textbf{103}, 67001 (2013)], which captures the canonical electron-hole-doping phase diagram of the iron-pnictide BaFe$_{2}$As$_{2}$, we study the evolution of quasiparticle states
Recent measurements of Fermi surface with de Haas-van Alphen oscillations in LaFePO showed a shrinking of the Fermi pockets with respect to first-principle LDA calculations, suggesting an energy shift of the hole and electrons bands with respect to L
The wave-vector q and doping (x,y) dependences of the magnetic energy, iron moment, and effective exchange interactions in LaFeAsO{1-x}F{x} and Ba{1-2y}K{2y}Fe2As2 are studied by self-consistent LSDA calculations for co-planar spin spirals. For the u
We studied two BaFe2-xNixAs2 (Ni-doped Ba-122) single crystals at two dfferent doping levels (underdoped and optimally doped) using an optical spectroscopic technique. The underdoped sample shows a magnetic phase transition around 80 K. We analyze th
We report on a comprehensive de Haas--van Alphen (dHvA) study of the iron pnictide LaFe$_2$P$_2$. Our extensive density-functional band-structure calculations can well explain the measured angular-dependent dHvA frequencies. As salient feature, we ob