TY - JOUR
T1 - Realization of Enhanced Magnetoelectric Coupling and Raman Spectroscopic Signatures in 0-0 Type Hybrid Multiferroic Core-Shell Geometric Nanostructures
AU - Abraham, Ann Rose
AU - Raneesh, B.
AU - Woldu, Tesfakiros
AU - Aškrabić, Sonja
AU - Lazović, Saša
AU - Dohčević-Mitrović, Zorana
AU - Oluwafemi, Oluwatobi Samuel
AU - Thomas, Sabu
AU - Kalarikkal, Nandakumar
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2017/1/30
Y1 - 2017/1/30
N2 - Multiferroic heterostructures' contribution to the persistent growth of ultrafast wireless communications may pave the way for future 5G technology. In line with this, we herein report the development of an engineered hybrid multiferroic core-shell nanostructure with a soft magnetic core and a ferroelectric shell. In this system, the attributes of the ferromagnetic core were modulated by a ferroelectric coating over it, in order to impart a bifunctionality to it and thus induce magnetoelectric coupling in it for multifunctional device applications. The phase, crystal structure and morphology of these composites have been investigated using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and confocal Raman spectroscopy. The origin of strain mediated magnetoelectric coupling effect at the ferromagnetic core and ferroelectric shell interface was also investigated. Raman spectroscopy is efficiently utilized to manifest the multiferroism in the core-shell samples. High resolution transmission electron microscopy images and domain structure mapping using confocal Raman microscopy along with Raman images substantiate the core-shell nature of the samples. The findings manifest how tuning of the ferromagnetic phase influences the magnetoelectric coupling at the interface and reveal novel approaches for manipulating the attributes of a ferromagnetic-ferroelectric interface for innovative device applications. The outcome of the experiments indicates an energy efficient move toward the control of the E-field by the magnetic field, which demonstrates an enormous prospective for novel low power electronic, magnonic, and spintronic devices.
AB - Multiferroic heterostructures' contribution to the persistent growth of ultrafast wireless communications may pave the way for future 5G technology. In line with this, we herein report the development of an engineered hybrid multiferroic core-shell nanostructure with a soft magnetic core and a ferroelectric shell. In this system, the attributes of the ferromagnetic core were modulated by a ferroelectric coating over it, in order to impart a bifunctionality to it and thus induce magnetoelectric coupling in it for multifunctional device applications. The phase, crystal structure and morphology of these composites have been investigated using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and confocal Raman spectroscopy. The origin of strain mediated magnetoelectric coupling effect at the ferromagnetic core and ferroelectric shell interface was also investigated. Raman spectroscopy is efficiently utilized to manifest the multiferroism in the core-shell samples. High resolution transmission electron microscopy images and domain structure mapping using confocal Raman microscopy along with Raman images substantiate the core-shell nature of the samples. The findings manifest how tuning of the ferromagnetic phase influences the magnetoelectric coupling at the interface and reveal novel approaches for manipulating the attributes of a ferromagnetic-ferroelectric interface for innovative device applications. The outcome of the experiments indicates an energy efficient move toward the control of the E-field by the magnetic field, which demonstrates an enormous prospective for novel low power electronic, magnonic, and spintronic devices.
UR - http://www.scopus.com/inward/record.url?scp=85021248416&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.6b12461
DO - 10.1021/acs.jpcc.6b12461
M3 - Article
AN - SCOPUS:85021248416
SN - 1932-7447
VL - 121
SP - 4352
EP - 4362
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 8
ER -