Ferromagnetic stability optimization via oxygen-vacancy control in single-atom Co/TiO(2) nanostructures

通过控制单原子Co/TiO(2)纳米结构中的氧空位来优化铁磁稳定性

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Abstract

Oxygen vacancies and their correlation with the nanomagnetism and electronic structure are crucial for applications in dilute magnetic semiconductors design applications. Here, we report on cobalt single atom-incorporated titanium dioxide (TiO(2)) monodispersed nanoparticles synthesized using a thermodynamic redistribution strategy. Using advanced synchrotron-based X-ray techniques and simulations, we find trivalent titanium is absent, indicating trivalent cations do not influence ferromagnetic (FM) stability. Density functional theory calculations show that the FM stability between Co(2+) ions is very weak. However, electron doping from additional oxygen vacancies can significantly enhance this FM stability, which explains the observed room-temperature ferromagnetism. Moreover, our calculations illustrate enhanced FM interactions between Co(Ti) + V(O) complexes with additional oxygen vacancies. This study explores the electronic structure and room-temperature ferromagnetism using monodispersed nanocrystallites with single-atom-incorporated TiO(2) nanostructures. The strategies described herein offer promise in revealing magnetism in other single-atom-incorporated nanostructures.

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