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Register a new userPhase Separation and Magnetic Order in K-doped Iron Selenide Superconductor
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Alkali-doped iron selenide is the latest member of high Tc superconductor family, and its peculiar characters have immediately attracted extensive attention. We prepared high-quality potassium-doped iron selenide (KxFe2-ySe2) thin films by molecular beam epitaxy and unambiguously demonstrated the existence of phase separation, which is currently under debate, in this material using scanning tunneling microscopy and spectroscopy. The stoichiometric superconducting phase KFe2Se2 contains no iron vacancies, while the insulating phase has a surd5timessurd5 vacancy order. The iron vacancies are shown always destructive to superconductivity in KFe2Se2. Our study on the subgap bound states induced by the iron vacancies further reveals a magnetically-related bipartite order in the superconducting phase. These findings not only solve the existing controversies in the atomic and electronic structures in KxFe2-ySe2, but also provide valuable information on understanding the superconductivity and its interplay with magnetism in iron-based superconductors.
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We elucidate the existing controversies in the newly discovered K-doped iron selenide (KxFe2-ySe2-z) superconductors. The stoichiometric KFe2Se2 with surd2timessurd2 charge ordering was identified as the parent compound of KxFe2-ySe2-z superconductor using scanning tunneling microscopy and spectroscopy. The superconductivity is induced in KFe2Se2 by either Se vacancies or interacting with the anti-ferromagnetic K2Fe4Se5 compound. Totally four phases were found to exist in KxFe2-ySe2-z: parent compound KFe2Se2, superconducting KFe2Se2 with surd2timessurd5 charge ordering, superconducting KFe2Se2-z with Se vacancies and insulating K2Fe4Se5 with surd5timessurd5 Fe vacancy order. The phase separation takes place at the mesoscopic scale under standard molecular beam epitaxy condition.
The phenomenon of phase separation into antiferromagnetic (AFM) and superconducting (SC) or normal-state regions has great implication for the origin of high-temperature (high-Tc) superconductivity. However, the occurrence of an intrinsic antiferromagnetism above the Tc of (Li, Fe)OHFeSe superconductor is questioned. Here we report a systematic study on a series of (Li, Fe)OHFeSe single crystal samples with Tc up to ~41 K. We observe an evident drop in the static magnetization at Tafm ~125 K, in some of the SC (Tc < ~38 K, cell parameter c < ~9.27 {AA}) and non-SC samples. We verify that this AFM signal is intrinsic to (Li, Fe)OHFeSe. Thus, our observations indicate mesoscopic-to-macroscopic coexistence of an AFM state with the normal (below Tafm) or SC (below Tc) state in (Li, Fe)OHFeSe. We explain such coexistence by electronic phase separation, similar to that in high-Tc cuprates and iron arsenides. However, such an AFM signal can be absent in some other samples of (Li, Fe)OHFeSe, particularly it is never observed in the SC samples of Tc > ~38 K, owing to a spatial scale of the phase separation too small for the macroscopic magnetic probe. For this case, we propose a microscopic electronic phase separation. It is suggested that the microscopic static phase separation reaches vanishing point in high-Tc (Li, Fe)OHFeSe, by the occurrence of two-dimensional AFM spin fluctuations below nearly the same temperature as Tafm reported previously for a (Li, Fe)OHFeSe (Tc ~42 K) single crystal. A complete phase diagram is thus established. Our study provides key information of the underlying physics for high-Tc superconductivity.
Here we present a combined study of the slightly underdoped novel pnictide superconductor Ba(1-x)K(x)Fe(2)As(2) by means of X-ray powder diffraction, neutron scattering, muon spin rotation (muSR), and magnetic force microscopy (MFM). Commensurate static magnetic order sets in below Tm ~ 70 K as inferred from the emergence of the magnetic (1 0 -3) reflection in the neutron scattering data and from the observation of damped oscillations in the zero-field-muSR asymmetry. Transverse-field muSR below Tc shows a coexistence of magnetically ordered and non-magnetic states, which is also confirmed by MFM imaging. We explain such coexistence by electronic phase separation into antiferromagnetic and superconducting/normal state regions on a lateral scale of several tens of nanometers. Our findings indicate that such mesoscopic phase separation can be considered an intrinsic property of some iron pnictide superconductors.
In Ba(Fe0.95Co0.05)2As2 all of the 75As NMR intensity at the paramagnetic resonance position vanishes abruptly below Tonset(SDW)=56 K, indicating that magnetic (spin density wave) order is present in all of the sample volume, despite bulk superconductivity below Tc=15 K. The two phases thus coexist homogeneously at the microscopic scale. In Ba0.6K0.4Fe2As2, on the other hand, the signal loss below Tonset(SDW)~75 K is not complete, revealing that magnetic order is bound to finite-size areas of the sample, while the remaining NMR signal shows a clear superconducting response below Tc=37 K. Thus, the two phases are not homogeneously mixed, at least for this potassium concentration. For both samples, spatial electronic and/or magnetic inhomogeneity is shown to characterize the NMR properties in the normal state.
Nematic phase intertwines closely with high-Tc superconductivity in iron-based superconductors. Its mechanism, which is closely related to the pairing mechanism of superconductivity, still remains controversial. Comprehensive characterization of how the electronic state reconstructs in the nematic phase is thus crucial. However, most experiments focus only on the reconstruction of band dispersions. Another important characteristic of electronic state, the spectral weight, has not been studied in details so far. Here, we studied the spectral weight transfer in the nematic phase of FeSe$_{0.9}$S$_{0.1}$ using angle-resolved photoemission spectroscopy and in-situ detwinning technique. There are two elliptical electron pockets overlapping with each other orthogonally at the Brillouin zone corner. We found that, upon cooling, one electron pocket loses spectral weight and fades away, while the other electron pocket gains spectral weight and becomes pronounced. Our results show that the symmetry breaking of electronic state is manifested by not only the anisotropic band dispersion but also the band-selective modulation of spectral weight. Our observation completes our understanding of the nematic electronic state, and put strong constraints on the theoretical models. It further provide crucial clues to understand the gap anisotropy and orbital-selective pairing in iron-selenide superconductors.
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