Giant Controllable Magnetization Changes Induced by Structural Phase Transitions in a Metamagnetic Artificial Multiferroic

S. P. Bennett, A. T. Wong, A. Glavic, A. Herklotz, C. Urban, I. Valmianski, M. D. Biegalski, H. M. Christen, T. Z. Ward, V. Lauter

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42 Scopus citations

Abstract

The realization of a controllable metamagnetic transition from AFM to FM ordering would open the door to a plethora of new spintronics based devices that, rather than reorienting spins in a ferromagnet, harness direct control of a materials intrinsic magnetic ordering. In this study FeRh films with drastically reduced transition temperatures and a large magneto-thermal hysteresis were produced for magnetocaloric and spintronics applications. Remarkably, giant controllable magnetization changes (measured to be as high has ∼25%) are realized by manipulating the strain transfer from the external lattice when subjected to two structural phase transitions of BaTiO3 (001) single crystal substrate. These magnetization changes are the largest seen to date to be controllably induced in the FeRh system. Using polarized neutron reflectometry we reveal how just a slight in plane surface strain change at ∼290C results in a massive magnetic transformation in the bottom half of the film clearly demonstrating a strong lattice-spin coupling in FeRh. By means of these substrate induced strain changes we show a way to reproducibly explore the effects of temperature and strain on the relative stabilities of the FM and AFM phases in multi-domain metamagnetic systems. This study also demonstrates for the first time the depth dependent nature of a controllable magnetic order using strain in an artificial multiferroic heterostructure.

Original languageEnglish
Article number22708
JournalScientific Reports
Volume6
DOIs
StatePublished - 2016

Funding

This work was supported by the Scientific User Facilities Division, the Office of Basic Energy Sciences (BES), US Department of Energy (DOE), (S.B., V.L., A.G. & H.C.). This effort was also supported in part by the US Department of Energy (DOE), Office of Basic Energy Sciences (BES), Materials Sciences and Engineering Division, (T.Z.W. and A.H.) and under US DOE grant DE-SC0002136 (A.W.). And grant DE FG02 87ER-45332, DMS funded by the Department of Energy’s Office of Basic Energy Science, (C. U. & I. V.).

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