Frustration-driven C4 symmetric orders in a hetero-structured iron-based superconductor

التفاصيل البيبلوغرافية
العنوان: Frustration-driven C4 symmetric orders in a hetero-structured iron-based superconductor
المؤلفون: Ok, Jong Mok, Baek, S. -H., Hoch, C., Kremer, R. K., Park, S. Y., Ji, Sungdae, Buechner, B., Park, J. -H., Hyun, S. I., Shim, J. H., Bang, Yunkyu, Moon, E. G., Mazin, I. I., Kim, Jun Sung
سنة النشر: 2017
المجموعة: Condensed Matter
مصطلحات موضوعية: Condensed Matter - Superconductivity, Condensed Matter - Materials Science, Condensed Matter - Strongly Correlated Electrons
الوصف: A subtle balance between competing interactions in strongly correlated systems can be easily tipped by additional interfacial interactions in a heterostructure. This often induces exotic phases with unprecedented properties, as recently exemplified by high-Tc superconductivity in FeSe monolayer on the nonmagnetic SrTiO3. When the proximity-coupled layer is magnetically active, even richer phase diagrams are expected in iron-based superconductors (FeSCs), which however has not been explored due to the lack of a proper material system. One promising candidate is Sr2VO3FeAs, a naturally-assembled heterostructure of a FeSC and a Mott-insulating vanadium oxide. Here, using high-quality single crystals and high-accuracy 75As and 51V nuclear magnetic resonance (NMR) measurements, we show that a novel electronic phase is emerging in the FeAs layer below T0 ~ 155 K without either static magnetism or a crystal symmetry change, which has never been observed in other FeSCs. We find that frustration of the otherwise dominant Fe stripe and V Neel fluctuations via interfacial coupling induces a charge/orbital order with C4-symmetry in the FeAs layers, while suppressing the Neel antiferromagnetism in the SrVO3 layers. These findings demonstrate that the magnetic proximity coupling is effective to stabilize a hidden order in FeSCs and, more generally, in strongly correlated heterostructures.
Comment: 8 pages, 4 figures
نوع الوثيقة: Working Paper
URL الوصول: http://arxiv.org/abs/1706.08157
رقم الانضمام: edsarx.1706.08157
قاعدة البيانات: arXiv