Keep up to date with the latest research and developments from Diamond. Sign up for news on our scientific output, facility updates and plans for the future.
Spin-orbit torque (SOT) arises from spin-orbit coupling in heavy metal/ferromagnet bilayers, and can be used to control the magnetisation direction. It is of considerable interest as a way to efficiently switch the magnetisation of spintronic devices, which have advantages over traditional electronic devices, including non-volatile memory and logic applications. In order to engineer materials with enhanced SOT, for lower power consumption, scientists are investigating the microscopic origin of SOT.
A team of researchers based in Korea and the UK used X-ray Absorption Spectroscopy (XAS) and X-ray Magnetic Circular Dichroism (XMCD) measurements on Diamond’s BLADE: X-ray Dichroism and Scattering beamline (I10) to investigate the relationship between the resistivity and the spin-Hall angle of platinum. They found that the SOT strength increases with heavy metal resistivity. Their results are expected to provide an efficient route for material engineering towards improved SOT-based spintronic devices.
The manipulation of the magnetisation by in-plane current utilising spin-orbit torque (SOT) has been receiving a great deal of attention due to its possible applications in spintronic devices such as magnetic memories and spin-logic devices1-3. For wider applications of spintronic devices, it is essential to find an efficient way to switch the magnetisation. In this respect, many attempts are being made in order to improve the SOT efficiency, for instance, by finding heavy metal (HM) electrodes with high spin Hall angle.
It has been experimentally shown that the θSH,eff of Pt increases with the Pt resistivity, however, the enhancement factor of the spin-Hall angle is 3.0 while the enhancement factor of the Pt resistivity is 1.6. This may imply that there is a significant interface contribution to the enhancement in θSH,eff since more current flows near the Co/Pt interface as the Pt resistivity increases. To account for this additional contribution to the SOT, the interface contribution needed to be experimentally addressed, which is related to the spin-orbit coupling-induced band splitting originating from the inversion-symmetry breaking at the interface. X-ray Absorption Spectroscopy (XAS) and X-ray Magnetic Circular Dichroism (XMCD) measurements were performed to verify whether the interface spin-orbit coupling is influenced by the Pt resistivity. Two quantities associated with the spin-orbit coupling of the Co atoms were obtained: the branching ratio (B) and the orbital-to-spin magnetic moment ratio (mL/mS,eff) using the XAS and XMCD spectra and their integrated intensities for Pt(5 nm)/Co(0.8 nm)/AlOx (1.8 nm) samples (Fig. 2a,b). The obtained values of B and mL/mS,eff show a gradual increase with Pt resistivity indicating that the spin-orbit interaction of the Co indeed increases with the resistivity of the Pt layer. These results are in good agreement with the theoretical prediction4 which emphasises the important role of interfacial spin-orbit interaction that contributes to the increase in θSH,eff. Therefore, our result, the efficient control of θSH,eff and hence of SOT by controlling the HM resistivity, opens up a novel way to improve the switching efficiency in SOT-active devices.
Funding acknowledgement: This work was supported by the National Research Foundation of Korea (2017R1A2A2A05069760, 2017M2A2A6A01071238)
Diamond Light Source is the UK's national synchrotron science facility, located at the Harwell Science and Innovation Campus in Oxfordshire.
Copyright © 2022 Diamond Light Source
Diamond Light Source Ltd
Diamond House
Harwell Science & Innovation Campus
Didcot
Oxfordshire
OX11 0DE
Diamond Light Source® and the Diamond logo are registered trademarks of Diamond Light Source Ltd
Registered in England and Wales at Diamond House, Harwell Science and Innovation Campus, Didcot, Oxfordshire, OX11 0DE, United Kingdom. Company number: 4375679. VAT number: 287 461 957. Economic Operators Registration and Identification (EORI) number: GB287461957003.