Search for: All records

Abstract Colloidal magnetite nanoparticles self‐assemble onto a disk drive medium as directed by magnetic field gradients created where the medium magnetic moment switches direction over single nanometer distances. Here, it is shown that for two such reversals or transitions that are closely spaced, the nanoparticles self‐assemble into a single feature centered between the transitions, rather than forming separate features at the transitions, and the resulting 2D assembly achieves hexatic ordering. Langevin dynamics simulations are used to explain these results, and it is found that the detailed magnetic properties of the medium play a critical role in determining assembly location. Slight changes to solvent polarity disrupt the hexatic ordering and push the nanoparticles toward the transitions, suggesting an alternate mechanism to precisely tune the self‐assembly process. 

The agglomeration of ferromagnetic nanoparticles in a fluid is studied using nanoparticle-level Langevin dynamics simulations. The simulations have interdigitation and bridging between ligand coatings included using a computationally-cheap, phenomenological sticking parameter c. The interactions between ligand coatings are shown in this preliminary study to be important in determining the shapes of agglomerates that form. A critical size for the sticking parameter is estimated analytically and via the simulations and indicates where particle agglomerates transition from well-ordered (c is small) to disordered (c is large) shapes. Results are also presented for the hysteresis loops (magnetization versus applied field) for these particle systems in an oscillating magnetic field appropriate for hyperthermia applications. The results show that the clumping of particles has a significant effect on their macroscopic properties, with important consequences on applications. In particular, the work done by an oscillating field on the system has a nonmonotonic dependence on c.