Abstract
Magneto-ionics has emerged as a promising approach to manipulate magnetic properties, not only by drastically reducing power consumption associated with electric current based devices but also by enabling novel functionalities. To date, magneto-ionics have been mostly explored in oxygen-based systems, while there is a surge of interests in alternative ionic systems. Here we demonstrate highly effective hydroxide-based magneto-ionics in electrodeposited α-Co(OH)2 films. The α-Co(OH)2, which is a room temperature paramagnet, is switched to ferromagnetic after electrolyte gating with a negative voltage. The system is fully, magnetically reversible upon positive voltage application. The origin of the reversible paramagnetic-to-ferromagnetic transition is attributed to the ionic diffusion of hydroxyl groups, promoting the formation of metallic cobalt ferromagnetic regions. Our findings demonstrate one of the lowest turn-on voltages reported for propylene carbonate gated experiments. By tuning the voltage magnitude and sample area we demonstrate that the speed of the induced ionic effect can be drastically enhanced.
Original language | English (US) |
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Journal | Journal of Materials Chemistry |
State | Published - 2022 |
Bibliographical note
KAUST Repository Item: Exported on 2022-11-04Acknowledged KAUST grant number(s): OSR-2019-CRG8-4081
Acknowledgements: This work has been supported in part by SMART (2018-NE-2861), one of seven centers of nCORE, a Semiconductor Research Corporation program, sponsored by National Institute of Standards and Technology (NIST), the NSF (ECCS-1933527, ECCS-2151809), and KAUST (OSR-2019-CRG8-4081). A.A.F. acknowledges support from the NSF-REU program (DMR- 1659532). The acquisition of a Magnetic Property Measurements System (MPMS3), which was used in this investigation was supported by the NSF-MRI program (DMR-1828420).