Please use this identifier to cite or link to this item: https://doi.org/10.1039/c7tc02664a
Title: Single-layer metal halides MX2 (X = Cl, Br, I): Stability and tunable magnetism from first principles and Monte Carlo simulations
Authors: Kulish V.V. 
Huang W. 
Keywords: Calculations
Intelligent systems
Ising model
Magnetic properties
Magnetism
Metal halides
Antiferromagnetics
First principles
First-principles calculation
Magnetic transitions
Nanospintronics
Nearest neighbors
Single-layer metal
Thermal dependences
Monte Carlo methods
Issue Date: 2017
Citation: Kulish V.V., Huang W. (2017). Single-layer metal halides MX2 (X = Cl, Br, I): Stability and tunable magnetism from first principles and Monte Carlo simulations. Journal of Materials Chemistry C 5 (34) : 8734-8741. ScholarBank@NUS Repository. https://doi.org/10.1039/c7tc02664a
Abstract: Based on first-principles calculations, we investigate a novel class of 2D materials-MX2 metal dihalides (X = Cl, Br, I). Our results show that single-layer dihalides are energetically and dynamically stable and can be potentially exfoliated from their bulk layered forms. We found that 2D FeX2, NiX2, CoCl2 and CoBr2 monolayers are ferromagnetic (FM), while VX2, CrX2, MnX2 and CoI2 are antiferromagnetic (AFM). The magnetic properties of 2D dihalides originate from the competition between AFM direct nearest-neighbor d-d exchange and FM superexchange via halogen p states, which leads to a variety of magnetic states. The thermal dependence of magnetic properties and the Curie temperature of magnetic transition are evaluated using statistical Monte Carlo simulations based on the Ising model with classical Heisenberg Hamiltonian. The magnetic properties of single-layer dihalides can be further tuned by strain and carrier doping. Our study broadens the family of existing 2D materials with promising applications in nanospintronics. © 2017 The Royal Society of Chemistry.
Source Title: Journal of Materials Chemistry C
URI: https://scholarbank.nus.edu.sg/handle/10635/173959
ISSN: 20507534
DOI: 10.1039/c7tc02664a
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