5 years ago

Intrinsic Ferromagnetism in Mn-Substituted MoS2 Nanosheets Achieved by Supercritical Hydrothermal Reaction

Intrinsic Ferromagnetism in Mn-Substituted MoS2 Nanosheets Achieved by Supercritical Hydrothermal Reaction
Peng Guo, Liang Cai, Shiqiang Wei, Chao Ma, Qinghua Liu, Hengli Duan, Chao Wang, Hao Tan, Wensheng Yan, Wei Hu, Xusheng Zheng, Fengchun Hu, Zhihu Sun
Doping atomically thick nanosheets is a great challenge due to the self-purification effect that drives the precipitation of dopants. Here, a breakthrough is made to dope Mn atoms substitutionally into MoS2 nanosheets in a sulfur-rich supercritical hydrothermal reaction environment, where the formation energy of Mn substituting for Mo sites in MoS2 is significantly reduced to overcome the self-purification effect. The substitutional Mn doping is convincingly evidenced by high-angle annular dark-field scanning transmission electron microscopy and X-ray absorption fine spectroscopy characterizations. The Mn-doped MoS2 nanosheets show robust intrinsic ferromagnetic response with a saturation magnetic moment of 0.05 µB Mn−1 at room temperature. The intrinsic ferromagnetism is further confirmed by the reversibility of the magnetic behavior during the cycle of incorporating/removing Li codopants, showing the critical role of Mn 3d electronic states in mediating the magnetic interactions in MoS2 nanosheets. A supercritical hydrothermal reaction method is used to substitutionally dope Mn atoms into MoS2 nanosheets, as convincingly evidenced by high-angle annular dark-field and X-ray absorption fine spectroscopy characterizations. The as-prepared nanosheets show robust intrinsic ferromagnetic response with a saturation magnetic moment of 0.05 µB Mn−1 at room temperature, which can be tuned by reversible incorporation/removal of Li codopants.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/smll.201701389

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.