Electronic reconstruction in confined SrRuO3 monolayers

被引:0
作者
Lamichhane, U. [1 ]
Sankhi, B. [1 ]
Kundu, N. [1 ]
Fabbris, G. [2 ]
Choi, Y. [2 ]
Haskel, D. [2 ]
Mcchesney, J. L. [2 ]
Cao, Yue [3 ]
Li, J. [4 ]
Bisogni, V. [4 ]
Borunda, M. F. [1 ]
Meyers, D. [1 ]
机构
[1] Oklahoma State Univ, Dept Phys, Stillwater, OK 74078 USA
[2] Argonne Natl Lab, Adv Photon Source, Lemont, IL 60439 USA
[3] Argonne Natl Lab, Mat Sci Div, Lemont, IL 60439 USA
[4] Brookhaven Natl Lab, NSLS 2, Upton, NY 11973 USA
基金
美国国家科学基金会;
关键词
TRANSITION-METAL; BRANCHING RATIO; BAND-STRUCTURE; SR2RUO4; OXIDE; INSULATOR; MAGNETISM; PHYSICS; SUPERCONDUCTIVITY; HETEROSTRUCTURES;
D O I
10.1103/PhysRevB.110.235104
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We report the observation of an electronic reconstruction in dimensionally controlled ruthenate heterostructures synthesized by pulsed laser deposition. High structural and electronic quality of superlattices comprised of a single SrRuO3 layer inter-spaced with varying thicknesses of insulating SrTiO3 layers was verified by reflection high energy electron diffraction, atomic force microscopy, x-ray diffraction, reciprocal space mapping, and x-ray absorption spectroscopy. X-ray absorption spectroscopy evidences a confinement-driven evolution of the Ru electronic configuration from the d 5 L to the d 4 state. Significant increases of the spin-orbit coupling are observed in connection with the configuration changes supporting recent works identifying large enhancement of the magnetic anisotropy. The growth of high quality two-dimensional confined ruthenate layers under precisely controlled environments highlights the potential to directly manipulate interlayer coupling and selectively perturb the electronic state in ruthenates in analogy to superconducting Sr2RuO4.
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页数:10
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