Spontaneously induced magnetic anisotropy in an ultrathin Co/MoS2 heterojunction. Issue 7 (13th May 2020)
- Record Type:
- Journal Article
- Title:
- Spontaneously induced magnetic anisotropy in an ultrathin Co/MoS2 heterojunction. Issue 7 (13th May 2020)
- Main Title:
- Spontaneously induced magnetic anisotropy in an ultrathin Co/MoS2 heterojunction
- Authors:
- Lu, Chun-I
Huang, Chih-Heng
Ou Yang, Kui-Hon
Simbulan, Kristan Bryan
Li, Kai-Shin
Li, Feng
Qi, Junjie
Jugovac, Matteo
Cojocariu, Iulia
Feyer, Vitaliy
Tusche, Christian
Lin, Minn-Tsong
Chuang, Tzu-Hung
Lan, Yann-Wen
Wei, Der-Hsin - Abstract:
- Abstract : MoS2 is predicted to be magnetized through charge and spin donation from the attached Co layer. In this work, we observe that the top amorphous Co layer has spontaneous magnetic anisotropy, and the domain walls follow the crystalline axis of MoS2 . Abstract : Magnetic anisotropy (MA) is a material preference that involves magnetization aligned along a specific direction and provides a basis for spintronic devices. Here we report the first observation of strong MA in a cobalt–molybdenum disulfide (Co/MoS2 ) heterojunction. Element-specific magnetic images recorded with an X-ray photoemission electron microscope (PEEM) reveal that ultrathin Co films, of thickness 5 monolayers (ML) and above, form micrometer (μm)-sized domains on monolayer MoS2 flakes of size tens of μm. Image analysis shows that the magnetization of these Co domains is oriented not randomly but in directions apparently correlated with the crystal structure of the underlying MoS2 . Evidence from micro-area X-ray photoelectron spectra (μ-XPS) further indicates that a small amount of charge is donated from cobalt to sulfur upon direct contact between Co and MoS2 . As the ferromagnetic behavior found for Co/MoS2 is in sharp contrast with that reported earlier for non-reactive Fe/MoS2, we suggest that orbital hybridization at the interface is what makes Co/MoS2 different. Our report provides micro-magnetic and micro-spectral evidence that consolidates the knowledge required to build functionalAbstract : MoS2 is predicted to be magnetized through charge and spin donation from the attached Co layer. In this work, we observe that the top amorphous Co layer has spontaneous magnetic anisotropy, and the domain walls follow the crystalline axis of MoS2 . Abstract : Magnetic anisotropy (MA) is a material preference that involves magnetization aligned along a specific direction and provides a basis for spintronic devices. Here we report the first observation of strong MA in a cobalt–molybdenum disulfide (Co/MoS2 ) heterojunction. Element-specific magnetic images recorded with an X-ray photoemission electron microscope (PEEM) reveal that ultrathin Co films, of thickness 5 monolayers (ML) and above, form micrometer (μm)-sized domains on monolayer MoS2 flakes of size tens of μm. Image analysis shows that the magnetization of these Co domains is oriented not randomly but in directions apparently correlated with the crystal structure of the underlying MoS2 . Evidence from micro-area X-ray photoelectron spectra (μ-XPS) further indicates that a small amount of charge is donated from cobalt to sulfur upon direct contact between Co and MoS2 . As the ferromagnetic behavior found for Co/MoS2 is in sharp contrast with that reported earlier for non-reactive Fe/MoS2, we suggest that orbital hybridization at the interface is what makes Co/MoS2 different. Our report provides micro-magnetic and micro-spectral evidence that consolidates the knowledge required to build functional heterojunctions based on two-dimensional (2D) materials. … (more)
- Is Part Of:
- Nanoscale horizons. Volume 5:Issue 7(2020)
- Journal:
- Nanoscale horizons
- Issue:
- Volume 5:Issue 7(2020)
- Issue Display:
- Volume 5, Issue 7 (2020)
- Year:
- 2020
- Volume:
- 5
- Issue:
- 7
- Issue Sort Value:
- 2020-0005-0007-0000
- Page Start:
- 1058
- Page End:
- 1064
- Publication Date:
- 2020-05-13
- Subjects:
- Nanoscience -- Periodicals
Nanotechnology -- Periodicals
620.505 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/nh#!recentarticles&adv ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d0nh00108b ↗
- Languages:
- English
- ISSNs:
- 2055-6756
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9829.980000
British Library DSC - BLDSS-3PM
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- 13865.xml