Depending on the solvent chosen, high temperatures can be used to control metal precursor reaction and the formation of magnetic NPs. It is versatile in controlling NP size, shape, structure and composition. [ 7 ] In this chemical context, two methods are commonly used. The fi rst one relays on the rapid injection of the reagents, which are often organometallic compounds, into hot surfactant solution, inducing the simultaneous formation of many nuclei ( Figure 1 ). Alternatively, reducing agents can be quickly added to metal salt solutions at high temperature. In both cases nucleation occurs when the monomer concentration is quickly increased over the critical supersaturation level; this nucleation stage relieves the supersaturation. [ 8 ] After the nucleation event, the preformed nuclei start to grow from the remaining monomers without additional nucleation events, leading to the formation of NPs. [ 9 ] To gain control of the NP size distribution, the nucleation events should occur simultaneously for all nucleating monomers, and the NP growth condition should be kept identical in the reaction solution. In the second common synthetic procedure, reagents are mixed at low temperature and the reaction is slowly heated in a controlled manner to generate nuclei. Subsequently, NP growth occurs by the addition of reactive species [ 7 ] or by Oswalt ripening, [ 9 ] where the high surface energy of the small NPs promotes their dissolution and the subsequent redeposition of the material on the larger NPs. These bottom-up approaches have proven to be very successful in the preparation of a large family of Fe and Co-based magnetic NPs.
Fe NPsMagnetic NPs based on metallic Fe have much higher magnetization values than their oxide counterparts (Fe, 218 emu g -1 ) [ 10 ] which is very attractive for biomedical applications like bioseparation, highly sensitive biosensing and MRI contrast enhancement. Although Fe NPs may be highly reactive in an aqueous environment, issues of biocompatibility, solubility, and stability can be addressed, for example, by coating the NPs with an inert inorganic layer and/or polymer. [ 11 ] Fe NPs are made by thermal decomposition and reduction of metal precursors followed by high temperature or other chemical treatments to form a robust shell of carbon, [ 12 ] oxides, [ 10,13 ] or noble metals. [ 14 ] It is well known that highly crystalline Fe NPs could be made by reduction of a dimeric iron precursor with H 2 ; however, once exposed to air, these NPs are