The origins of magnetism in transition-metal doped Na0.5Bi0.5TiO3 system are investigated by ab initio calculations. The calculated results indicate that a transition-metal atom sub- stitution for a Ti atom produces m...The origins of magnetism in transition-metal doped Na0.5Bi0.5TiO3 system are investigated by ab initio calculations. The calculated results indicate that a transition-metal atom sub- stitution for a Ti atom produces magnetic moments, which are due to the spin-polarization of transition-metal 3d electrons. The characteristics of exchange coupling are also calculated, which shows that in Cr-/Mn-/Fe-/Co- doped Na0.5Bi0.5TiO3 system, the antiferromagnetic coupling is favorable. The results can successfully explain the experimental phenomenon that, in Mn-/Fe- doped Nao.sBio.sTiO3 system, the ferromagnetism disappears at low tem- perature and the paramagnetic component becomes stronger with the increase of doping concentration of Mn/Fe/Co ions. Unexpectedly, we find the Na0.5Bi0.5Ti0.67V0.33iO3 sys- tem with ferromagnetic coupling is favorable and produces a magnetic moment of 2.00 P-B, which indicates that low temperature ferromagnetism materials could be made by intro- ducing V atoms in Na0.5Bi0.5TiO3. This may be a new way to produce low temperature multiferroic materials.展开更多
The combination effect of cation vacancies and O2 adsorption on ferromagnetism of Na0.5Bi0.5TiO3（100） surface is studied by using density functional theory. An ideal Na0.5Bi0.5TiO3（100） surface is non-magnetic and...The combination effect of cation vacancies and O2 adsorption on ferromagnetism of Na0.5Bi0.5TiO3（100） surface is studied by using density functional theory. An ideal Na0.5Bi0.5TiO3（100） surface is non-magnetic and the cation vacancy could induce the magnetism. By comparing the formation energies for Na, Bi and Ti vacancy, the Na vacancy is more stable than the others. Therefore, we focus on the configuration and electric structure for the system of O2 molecule adsorption on the Na0.5Bi0.5TiO3（100） surface with a Na vacancy. Among the five physisorption configurations we considered, the most likely adsorption position is Na vacancy. The O2 adsorption enhances the magnetism of the system. The contribution of spin polarization is mainly from the O 2p orbitals. The characteristics of exchange coupling are also calculated, which show that the ferromagnetic coupling is favorable. Compared with the previous calculation results, our calculations could explain the room-temperature ferromagnetism of Na0.5Bi0.5TiO3 nanocrytalline powders more reasonably, because of taking into account adsorbed oxygen and cation vacancies. Moreover, our results also show that adsorption of O2 molecule as well as introduction of cation vacancies may be a promising approach to improve multiferroic materials.展开更多
文摘The origins of magnetism in transition-metal doped Na0.5Bi0.5TiO3 system are investigated by ab initio calculations. The calculated results indicate that a transition-metal atom sub- stitution for a Ti atom produces magnetic moments, which are due to the spin-polarization of transition-metal 3d electrons. The characteristics of exchange coupling are also calculated, which shows that in Cr-/Mn-/Fe-/Co- doped Na0.5Bi0.5TiO3 system, the antiferromagnetic coupling is favorable. The results can successfully explain the experimental phenomenon that, in Mn-/Fe- doped Nao.sBio.sTiO3 system, the ferromagnetism disappears at low tem- perature and the paramagnetic component becomes stronger with the increase of doping concentration of Mn/Fe/Co ions. Unexpectedly, we find the Na0.5Bi0.5Ti0.67V0.33iO3 sys- tem with ferromagnetic coupling is favorable and produces a magnetic moment of 2.00 P-B, which indicates that low temperature ferromagnetism materials could be made by intro- ducing V atoms in Na0.5Bi0.5TiO3. This may be a new way to produce low temperature multiferroic materials.
基金supported by the National Natural Science Foundation of China (No.11547176, No.11704006)Henan College Key Research Project (No.15A140017)
文摘The combination effect of cation vacancies and O2 adsorption on ferromagnetism of Na0.5Bi0.5TiO3（100） surface is studied by using density functional theory. An ideal Na0.5Bi0.5TiO3（100） surface is non-magnetic and the cation vacancy could induce the magnetism. By comparing the formation energies for Na, Bi and Ti vacancy, the Na vacancy is more stable than the others. Therefore, we focus on the configuration and electric structure for the system of O2 molecule adsorption on the Na0.5Bi0.5TiO3（100） surface with a Na vacancy. Among the five physisorption configurations we considered, the most likely adsorption position is Na vacancy. The O2 adsorption enhances the magnetism of the system. The contribution of spin polarization is mainly from the O 2p orbitals. The characteristics of exchange coupling are also calculated, which show that the ferromagnetic coupling is favorable. Compared with the previous calculation results, our calculations could explain the room-temperature ferromagnetism of Na0.5Bi0.5TiO3 nanocrytalline powders more reasonably, because of taking into account adsorbed oxygen and cation vacancies. Moreover, our results also show that adsorption of O2 molecule as well as introduction of cation vacancies may be a promising approach to improve multiferroic materials.
