| Autor: |
Fan, Dong, Wang, Zhihao, Yin, Maoye, Li, Hengshuai, Hu, Haiquan, Guo, Feng, Feng, Zhenbao, Li, Jun, Zhang, Dong, Li, Zhi, Zhu, Minghui |
| Zdroj: |
Physical Chemistry Chemical Physics (PCCP); 12/7/2023, Vol. 25 Issue 45, p31257-31269, 13p |
| Abstrakt: |
Armchair X–N4 nanoribbons (X–AN4NRs) and zigzag X–N4 nanoribbons (X–ZN4NRs) were calculated using first-principles calculations. Ferromagnets (FM) were found to be the most stable among the initial magnetic structures. Furthermore, nanoribbons were found to be thermodynamically stable through molecular dynamics simulations. It can be found that when the temperature and total energy of X–AN4NRs and X–ZN4NRs change with time, they have a small oscillation range, which confirms the dynamic stability of X–AN4NRs and X–ZN4NRs under realistic experimental conditions. Subsequently, the magnetic moment analysis of the X–AN4NRs and X–ZN4NRs revealed that the magnetic moment of the X–AN4NRs is significantly smaller than that of X–ZN4NRs. The band structure and density of states (DOS) of the X–AN4NRs and X–ZN4NRs were also computed, which indicate different properties for different transition metal nanoribbons. The results suggest that different edge structures and transition metals can influence the electronic structure of the nanoribbons. Moreover, based on the band structure and DOS, it was found that Mn–AN4NRs and Fe–ZN4NRs exhibit half-metallic properties. They can generate 100% polarized currents at the Fermi level, providing valuable information for developing spintronic devices. Our study has a positive value for regulating the properties of the nanoribbons by metal atom substitution. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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