Abstract
Iron carbide nanoparticles (ICNPs) are considered to have great potential in new energy conversion, nanomagnets and biomedical applications due to their intrinsically peculiar magnetic and catalytic properties. However, the synthetic routes were greatly limited in morphology and phase controlled synthesis. In this article, we present a versatile solution chemistry route towards colloidal ICNPs (Fe(2)C-hexagonal and monoclinic syngony, Fe(5)C(2)-monoclinic syngony and Fe(3)C-orthorhombic syngony) derived from body centered cubic Fe@Fe(3)O(4) by introducing heteroatoms to restrain their phase transformation. We found that the phases of Fe(2)C NPs could be controlled by direct phase transformation in the drastic thermally driven procedure (defined as thermodynamical manner). Meanwhile, the selective adsorption of Cl ions weakened the bonding between Fe and C atoms, thus interfering with the penetration of C atoms to form lower carbon content Fe(5)C(2) and Fe(3)C NPs. The kinetic mechanisms were evaluated using density functional theory (DFT) simulations focusing on the bonding energy between Fe-C and Fe-Cl atoms. All the obtained ICNPs exhibited typically soft ferromagnetic properties with the highest saturation magnetization value of 101.2 emu g(-1) and the highest Curie temperature of 497.8 K.