Large-scale fabrication and Mo vacancy-induced robust room-temperature ferromagnetism of MoSe 2 thin films
Source abstract
Abstract
Molybdenum selenide (MoSe2) has recently attracted particular attention due to its room-temperature ferromagnetism (RTFM) and related spintronic applications. However, not only does the FM mechanism of MoSe2 remain controversial, but also the synthesis of MoSe2 thin films with robust RTFM is still an unmet challenge. Here it is shown that using polymer-assisted deposition under appropriate growth conditions, large-scale (4 cm × 4 cm) synthesis of MoSe2 thin films with robust RTFM and a smooth surface (roughness average ∼0.22 nm) is possible. A new record-high saturation magnetization (6.69 emu g-1) is achieved in the prepared MoSe2 thin films, about 5 times the previously reported record (1.39 emu g-1) obtained in 2H-MoSe2 nanoflakes. Meanwhile, the coercivity of the MoSe2 films can be tuned down to a new record-low value (5.0 Oe), one-tenth of the previously reported record. Notably, detailed analysis combining the experimental findings and calculation results shows that the robust RTFM mainly comes from the Ruderman-Kittel-Kasuya-Yoshida (RKKY) interaction between the magnetic moments induced by abundant Mo vacancies (VMos) in the MoSe2 films. Our results give insights into the large-scale production and robust RTFM of MoSe2 thin films and may provide a platform for designing and fabricating spintronic materials and devices based on transition-metal dichalcogenides.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: 2D Materials and Applications · Graphene research and applications · Heusler alloys: electronic and magnetic properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Physics, Sichuan University, Chengdu 610064, China
College of Physical Science and Technology, Lanzhou University, Lanzhou 730000, China
College of Optoelectronic Engineering, Chengdu University of Information Technology, Chengdu 610225, China
Funding
National Natural Science Foundation of China · National Key Research and Development Program of China
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