اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدRole of Arsenic in Iron-based Superconductivity at Atomic Scale
120
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
In iron-based superconductors, a unique tri-layer Fe-As (Se, Te, P) plays an essential role in controlling the electronic properties, especially the Cooper pairing interaction. Here we use scanning tunneling microscopy/spectroscopy (STM/S) to investigate the role of arsenic atom in superconducting Ba0.4K0.6Fe2As2 by directly breaking and restoring the Fe-As structure at atomic scale. After the up-As-layer peeled away, the tunneling spectrum of the exposed iron surface reveals a shallow incoherent gap, indicating a severe suppression of superconductivity without arsenic covering. When a pair of arsenic atoms is placed on such iron surface, a localized topographic feature is formed due to Fe-As orbital hybridization, and the superconducting coherent peaks recover locally with the gap magnitude the same as that on the iron-layer fully covered by arsenic. These observations unravel the Fe-As interactions on an atomic scale and imply its essential roles in the iron-based superconductivity.
قيم البحث
اقرأ أيضاً
Two-dimensional (2D) superconductors supply important platforms for exploring new quantum physics and high-$T_c$ superconductivity. The intrinsic superconducting properties in the 2D iron-arsenic superconductors are still unknown owing to the difficu
lties in the preparation of ultrathin samples. Here we report the fabrication and physical investigations of the high quality single-crystalline ultrathin films of the iron-arsenic superconductor KCa$_2$Fe$_4$As$_4$F$_2$. For the sample with the thickness of 2.6$sim$5 nm (1$sim$2 unit cells), a sharp superconducting transition at around 30 K (onset point) is observed. Compare with the bulk material, the ultrathin sample reveals a relatively lower $T_c$, wider transition width, and broader flux liquid region under the in-plane field. Moreover, the angle dependent upper critical field follows the Tinkham model, demonstrating the two-dimensional superconductivity in ultrathin KCa$_2$Fe$_4$As$_4$F$_2$.
Here we report pressure effect on superconducting transition temperature (Tc) of ReFeAsO0.85 (Re= Sm and Nd) system without fluorine doping. In-situ measurements under high pressure showed that Tc of the two compounds decrease monotonously over the p
ressure range investigated. The pressure coefficients dTc/dP in SmFeAsO0.85 and Nd FeAsO0.85 were different, revealing the important influence of the deformation in layers on Tc. Theoretical calculations suggested that the electron density of states decrease with increasing pressure, following the same trend of experimental data.
High-temperature iron-based superconductivity develops in a structure with unusual lattice-orbital geometry, based on a planar layer of Fe atoms with 3d orbitals and tetrahedrally coordinated by anions. Here we elucidate the electronic role of anions
in the iron-based superconductors utilizing state-of-the-art scanning tunneling microscopy. By measuring the local electronic structure, we find that As anion in Ba0.4K0.6Fe2As2 has a striking impact on the electron pairing. The superconducting electronic feature can be switched off/on by removing/restoring As atoms on Fe layer at the atomic scale. Our analysis shows that this remarkable atomic switch effect is related to the geometrical cooperation between anion mediated hopping and unconventional pairing interaction. Our results uncover that the local Fe-anion coupling is fundamental for the pairing interaction of iron-based superconductivity, and promise the potential of bottom-up engineering of electron pairing.
We report on the optimization of synthesis of iron-selenide (non-arsenic) superconducting powders that are based on 122 composition, with optimal Tc = 38 K and Jc = 10^5 A/cm2 (4 K). We also report on the wire proof-of concept for these materials, by
producing ~ 40 ft of wire that produce Ic. The 122 selenides are more difficult to synthesize and have more complex crystal structures compared to 11 selenides (FeSe and FeSe1-xTex), but they do offer higher Tc and might provoke a natural extension for 11 work.
The symmetry requirement and the origin of magnetic orders coexisting with superconductivity have been strongly debated issues of iron-based superconductors (FeSCs). Observation of C$_4$-symmetric antiferromagnetism in violation of the inter-band nes
ting condition of spin-density waves in superconducting ground state will require significant change in our understanding of the mechanism of FeSC. The superconducting material Sr$_2$VO$_3$FeAs, a bulk version of monolayer FeSC in contact with a perovskite layer with its magnetism (T$_N$ ~ 50 K) and superconductivity (T$_c$ ~ 37 K) coexisting at parent state, has no reported structural orthorhombic distortion and thus makes a perfect system to look for theoretically expected C$_4$ magnetisms. Based on variable temperature spin-polarized scanning tunneling microscopy (SPSTM) with newly discovered imaging mechanism that removes the static surface reconstruction (SR) pattern by fluctuating it rapidly with spin-polarized tunneling current, we could visualize underlying C$_4$ symmetric (2$times$2) magnetic domains and its phase domain walls. We find that this magnetic order is perfectly consistent with the plaquette antiferromagnetic order in tetragonal Fe spin lattice expected from theories based on the Heisenberg exchange interaction of local Fe moments and the quantum order by disorder. The inconsistency of its modulation Q vectors from the nesting condition also implies that the nesting-based C$_2$ symmetric magnetism is not a unique prerequisite of high-T$_c$ FeSC. Furthermore, the plaquette antiferromagnetic domain wall dynamics under the influence of small spin torque effect of spin-polarized tunneling current are shown to be consistent with theoretical simulation based on the extended Landau-Lifshitz-Gilbert equation.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
