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Polarity-tunable field-free room-temperature spin orbit torque switching via topological symmetry breaking in an all-vdW heterostructure for spin logic applications

  • Fan Gao
  • , Zili Wang
  • , Runyu Zhao
  • , Jing Li
  • , Xiaoyue Song
  • , Peiyuan Yu
  • , Yun Sun
  • , Weiran Xie
  • , Guodong Wei
  • , Yuan Yao
  • , Jin Zou
  • , Jie Zhang
  • , Shucheng Xing
  • , Roberto Mantovan
  • , Zongxia Guo
  • , Nicolas Jaouen
  • , Weisheng Zhao
  • , Tianxiao Nie*
  • *Corresponding author for this work
  • Beihang University
  • CAS - Institute of Physics
  • University of Queensland
  • National Research Council of Italy
  • L'Orme des Merisiers

Research output: Contribution to journalArticlepeer-review

Abstract

Two-dimensional ferromagnetic materials hold great promise for advancing low-power, high-integrated spintronic devices due to their atomic flat surfaces and versatile interfacial modulation. However, achieving a combination of room-temperature, field-free spin-orbit torque switching with tunable polarity in wafer-scale vdW heterostructures remains a significant challenge. Here, we demonstrate polarity-tunable, field-free spin-orbit torque switching in an all-vdW Bi2Te3/Fe4GeTe2 heterostructure, grown by molecular beam epitaxy. Interfacial coupling induces perpendicular magnetic anisotropy in Bi2Te3/Fe4GeTe2 interface, while the rest in-plane magnetic anisotropy component of Fe4GeTe2 breaks the inversion symmetry, enabling field-free switching. By modulating the direction of in-plane component, magnetic switching with different polarity could be achieved at low current density (~1.55×106 A/cm2). This allows for 16 reconfigurable Boolean logic functions in a single device, paving a pathway for energy-efficient 2D spintronic memory and logic systems. Our findings highlight the potential of all-vdW spin-orbit torque devices to revolutionize spintronics with scalable, room-temperature electronic control.

Original languageEnglish
Article number3826
JournalNature Communications
Volume17
Issue number1
DOIs
StatePublished - Dec 2026

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