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Abstract

Materials research has driven the development of modern nanoelectronic devices. In particular, research in magnetic thin films has revolutionized the development of spintronic devices1,2 because identifying new magnetic materials is key to better device performance and design. Van der Waals crystals retain their chemical stability and structural integrity down to the monolayer and, being atomically thin, are readily tuned by various kinds of gate modulation3,4. Recent experiments have demonstrated that it is possible to obtain two-dimensional ferromagnetic order in insulating Cr2Ge2Te6 (ref. 5) and CrI3 (ref. 6) at low temperatures. Here we develop a device fabrication technique and isolate monolayers from the layered metallic magnet Fe3GeTe2 to study magnetotransport. We find that the itinerant ferromagnetism persists in Fe3GeTe2 down to the monolayer with an out-of-plane magnetocrystalline anisotropy. The ferromagnetic transition temperature, Tc, is suppressed relative to the bulk Tc of 205 kelvin in pristine Fe3GeTe2 thin flakes. An ionic gate, however, raises Tc to room temperature, much higher than the bulk Tc. The gatetunable room-temperature ferromagnetism in two-dimensional Fe3GeTe2 opens up opportunities for potential voltage-controlled magnetoelectronics7-11 based on atomically thin van der Waals crystals.

Details

Title
Gate-tunable room-temperature ferromagnetism in two-dimensional Fe^sub 3^GeTe^sub 2^
Author
Deng, Yujun 1 ; Yu, Yijun 1 ; Song, Yichen 1 ; Zhang, Jingzhao 2 ; Wang, Nai Zhou 3 ; Sun, Zeyuan; Yi, Yangfan; Wu, Yi Zheng; Wu, Shiwei; Zhu, Junyi; Wang, Jing; Chen, Xian Hui; Zhang, Yuanbo

 State Key Laboratory of Surface Physics and Department of Physics, Fudan University, Shanghai, China 
 Department of Physics, The Chinese University of Hong Kong, Shatin, Hong Kong, China 
 Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing, China 
Pages
94-99,99A-99M
Section
LETTER
Publication year
2018
Publication date
Nov 1, 2018
Publisher
Nature Publishing Group
ISSN
00280836
e-ISSN
14764687
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2136860076
Copyright
Copyright Nature Publishing Group Nov 1, 2018